coding_sequence_variant	899817
inframe_insertion	bc966c
synonymous_variant	441fcf
start_lost	2178b9
stop_gained	2f4b44
CDS	cfd0df
exon	label
frameshift_variant	67bf84
missense_variant	attribute|CSQ:PolyPhen
sequence_variant	ff0000
3_prime_UTR_variant	abe5b6
inframe_deletion	adb578
splice_region_variant	5a5ad4
5_prime_UTR_variant	71c7d4

STARTFILTERS
missense_variant	CSQ:PolyPhen Contains probably_damaging
ENDFILTERS

GFF
CDS|ENST00000592782	VCF	inframe_insertion	194	194	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-72;AF_OTH=1.82548e-04;alleles=A%2CAGGGAAC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07030e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42611e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.09091e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.02292e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=14,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=inframe_insertion,Amino_acids=-/GN,HGVSp=ENSP00000468424.1:p.Asn25_Gly26dup,STRAND=1,CCDS=CCDS11494.1,Allele=GGGAAC,IMPACT=MODERATE,EXON=2/13,cDNA_position=194-195,CDS_position=63-64,SYMBOL=NMT1,VARIANT_CLASS=insertion,Protein_position=21-22,Codons=-/GGGAAC,MINIMISED=1,HGVSc=ENST00000592782.1:c.72_77dupGAACGG
CDS|ENST00000592782	VCF	inframe_insertion	204	204	0.0	.	.	AC_Male=5;AF_NFE=5.38871e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|2|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=5.01187e-60;AF_OTH=0.00000e+00;alleles=A%2CAACGGCC;AF_FIN=4.48994e-05;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84877e-05;Hom=0;AF_POPMAX=5.38871e-05;AN_POPMAX=111344;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|2|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=3.71261e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=3.80952e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80109e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.11301e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84241e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=ACGGCC:2.556e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=ACGGCC:4.635e-05,AFR_MAF=ACGGCC:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=ACGGCC:0,ENSP=ENSP00000468424,Consequence=inframe_insertion,Amino_acids=N/NGH,HGVSp=ENSP00000468424.1:p.Gly26_His27dup,STRAND=1,ExAC_SAS_MAF=ACGGCC:0,CCDS=CCDS11494.1,Allele=ACGGCC,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=ACGGCC:0,cDNA_position=204-205,CDS_position=73-74,ExAC_NFE_MAF=ACGGCC:0,SYMBOL=NMT1,Existing_variation=rs763191382,VARIANT_CLASS=insertion,Protein_position=25,Codons=aac/aACGGCCac,MINIMISED=1,ExAC_AFR_MAF=ACGGCC:2.471e-05,HGVSc=ENST00000592782.1:c.75_80dupCGGCCA,ExAC_Adj_MAF=ACGGCC:0
CDS|ENST00000592782	VCF	synonymous_variant	149	149	0.0	.	.	AC_Male=3;AF_NFE=3.60536e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|3|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00010e-44;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44872e-05;Hom=0;AF_POPMAX=5.96516e-05;AN_POPMAX=33528;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|2|1|0|0|0|1|0|0|0|0|0|0;AF_Male=2.23125e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.54132e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=2.71316e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43635e-05;Hom_Female=0;AF_AMR=5.96516e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:3.427e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:6.219e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000592782.1:c.18G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=149,CDS_position=18,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs776210749,VARIANT_CLASS=SNV,Protein_position=6,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000592782.1:c.18G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	155	155	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16473e-06;Hom=0;AF_POPMAX=6.50407e-05;AN_POPMAX=30750;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43837e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=6.00160e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50407e-05;AS_RF=9.41280e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592782.1:c.24A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=2/13,cDNA_position=155,CDS_position=24,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=gcA/gcG,HGVSc=ENST00000592782.1:c.24A>G
CDS|ENST00000592782	VCF	synonymous_variant	155	155	0.0	.	.	AC_Male=0;AF_NFE=9.01534e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-23;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08237e-06;Hom=0;AF_POPMAX=9.01534e-06;AN_POPMAX=110922;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.51046e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592782.1:c.24A>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=2/13,cDNA_position=155,CDS_position=24,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=gcA/gcC,HGVSc=ENST00000592782.1:c.24A>C
CDS|ENST00000592782	VCF	synonymous_variant	161	161	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-133;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08523e-06;Hom=0;AF_POPMAX=3.25373e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.44225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.78313e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=83;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25373e-05;AS_RF=8.78960e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.561e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=K,HGVSp=ENST00000592782.1:c.30G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=161,CDS_position=30,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs757761311,VARIANT_CLASS=SNV,Protein_position=10,Codons=aaG/aaA,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592782.1:c.30G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	167	167	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-56;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16067e-06;Hom=0;AF_POPMAX=6.50745e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48723e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.23810e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50745e-05;AS_RF=8.94107e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.542e-06&C:8.542e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0&C:1.55e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.36G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&C:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=T:0&C:0,cDNA_position=167,CDS_position=36,ExAC_NFE_MAF=T:0&C:0,SYMBOL=NMT1,Existing_variation=rs780444510,VARIANT_CLASS=SNV,Protein_position=12,Codons=ccG/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06&C:8.237e-06,HGVSc=ENST00000592782.1:c.36G>T,ExAC_Adj_MAF=T:0&C:0
CDS|ENST00000592782	VCF	synonymous_variant	177	177	0.0	.	.	AC_Male=1;AF_NFE=2.69721e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-37;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22188e-05;Hom=0;AF_POPMAX=2.69721e-05;AN_POPMAX=111226;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.42843e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.80333e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97663e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.515e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.545e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.46C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=177,CDS_position=46,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs748150811,VARIANT_CLASS=SNV,Protein_position=16,Codons=Ctg/Ttg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.46C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	185	185	0.0	.	.	AC_Male=0;AF_NFE=8.98828e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-59;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07106e-06;Hom=0;AF_POPMAX=8.98828e-06;AN_POPMAX=111256;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.77273e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00982e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05614e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=Q,HGVSp=ENST00000592782.1:c.54G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=2/13,cDNA_position=185,CDS_position=54,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=18,Codons=caG/caA,MINIMISED=1,HGVSc=ENST00000592782.1:c.54G>A
CDS|ENST00000592782	VCF	synonymous_variant	230	230	0.0	.	.	AC_Male=0;AF_NFE=9.00236e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.84034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07857e-06;Hom=0;AF_POPMAX=9.00236e-06;AN_POPMAX=111082;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.63736e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=13;AF_Female=9.02543e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.58906e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.666e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.57e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=C,HGVSp=ENST00000592782.1:c.99C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=230,CDS_position=99,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs762294220,VARIANT_CLASS=SNV,Protein_position=33,Codons=tgC/tgT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.99C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	233	233	0.0	.	.	AC_Male=0;AF_NFE=1.80050e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-23;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15614e-06;Hom=0;AF_POPMAX=1.80050e-05;AN_POPMAX=111080;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.76923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=1.80473e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.41561e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.741e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.152e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000592782.1:c.102G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=233,CDS_position=102,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768076232,VARIANT_CLASS=SNV,Protein_position=34,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592782.1:c.102G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	242	242	0.0	.	.	AC_Male=0;AF_NFE=9.01567e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.22517e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08407e-06;Hom=0;AF_POPMAX=9.01567e-06;AN_POPMAX=110918;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.97806e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.57456e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000592782.1:c.111G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=2/13,cDNA_position=242,CDS_position=111,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=37,Codons=gaG/gaA,MINIMISED=1,HGVSc=ENST00000592782.1:c.111G>A
CDS|ENST00000592782	VCF	synonymous_variant	251	251	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-88;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=1.02270e-04;AN_POPMAX=9778;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.40984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.02270e-04;DP_MEDIAN=61;AF_Female=9.06914e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.25490e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.018e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.120C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=251,CDS_position=120,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=40,Codons=agC/agT,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.120C>T,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	257	257	0.0	.	.	AC_Male=9;AF_NFE=7.26388e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|1|0|3|1|2|2|4|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-29;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.75899e-05;Hom=0;AF_POPMAX=9.84252e-05;AN_POPMAX=30480;AC_NFE=8;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|3|2|2|6|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=6.75017e-05;AF_AFR=0.00000e+00;AC_raw=15;AB_MEDIAN=4.19355e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=4.55506e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|13;Hom_raw=0;AF_SAS=9.84252e-05;AS_RF=9.10989e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=9.08540e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:0.0001008,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001161,AFR_MAF=T:0.0001995,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592782.1:c.126C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=257,CDS_position=126,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766535198,VARIANT_CLASS=SNV,Protein_position=42,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:9.060e-05,HGVSc=ENST00000592782.1:c.126C>T,ExAC_Adj_MAF=T:9.878e-05
CDS|ENST00000592782	VCF	synonymous_variant	272	272	0.0	.	.	AC_Male=148;AF_NFE=1.34979e-03;Hom_FIN=0;GQ_MEDIAN=80;AB_HIST_ALT=0|0|4|13|34|85|90|44|24|6|1|2|0|0|1|0|0|0|0|0;AC_FIN=74;DREF_MEDIAN=1.00000e-08;AF_OTH=1.30939e-03;alleles=T%2CC;AF_FIN=3.42910e-03;AC_OTH=7;Hom_Male=0;AC=275;Hom_NFE=0;AF=1.14690e-03;Hom=0;AF_POPMAX=3.42910e-03;AN_POPMAX=21580;AC_NFE=145;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|5|4|20|31|38|39|37|27|29|22|24|7|6|3|2|2|0|1;AF_Male=1.12191e-03;AF_AFR=1.81476e-03;AC_raw=304;AB_MEDIAN=3.07692e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=1.23127e-03;DP_MEDIAN=42;AF_Female=1.17747e-03;GQ_HIST_ALT=4|4|6|8|5|9|8|12|6|14|13|6|13|13|19|10|18|17|12|107;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=5.26862e-02;Hom_AMR=0;AC_EAS=6;AC_Female=127;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.51206e-04;AC_SAS=0;POPMAX=FIN;AC_POPMAX=74;AC_AFR=27;Hom_SAS=0;AC_ASJ=12;AF_raw=1.24619e-03;Hom_Female=0;AF_AMR=1.20409e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:0.001857,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0.001923,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0.001052,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.141T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0.005814,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=3/13,ExAC_AMR_MAF=C:0.001447,cDNA_position=272,CDS_position=141,ExAC_NFE_MAF=C:0.01002,SYMBOL=NMT1,Existing_variation=rs777402320,VARIANT_CLASS=SNV,Protein_position=47,Codons=agT/agC,MINIMISED=1,ExAC_AFR_MAF=C:1.911e-03,HGVSc=ENST00000592782.1:c.141T>C,ExAC_Adj_MAF=C:0.000438
CDS|ENST00000592782	VCF	synonymous_variant	332	332	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|1|2|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.10793e-31;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.78394e-05;Hom=0;AF_POPMAX=3.99467e-04;AN_POPMAX=15020;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|1|2|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.68939e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.91379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=4.11794e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.74988e-01;Hom_AMR=0;AC_EAS=6;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.99467e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.46164e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:6.366e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=G:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,EAS_MAF=G:0,EUR_MAF=G:0.003,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0.001103,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=G:0.0006,Amino_acids=K,HGVSp=ENST00000592782.1:c.201A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=3/13,ExAC_AMR_MAF=G:0,cDNA_position=332,CDS_position=201,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs141656657,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=67,AA_MAF=G:0,Codons=aaA/aaG,MINIMISED=1,ExAC_AFR_MAF=G:3.314e-05,HGVSc=ENST00000592782.1:c.201A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	335	335	0.0	.	.	AC_Male=0;AF_NFE=1.12471e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.76844e-06;Hom=0;AF_POPMAX=1.12471e-05;AN_POPMAX=88912;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.05753e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.93464e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10344e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.204C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/13,cDNA_position=335,CDS_position=204,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=68,Codons=ggC/ggT,MINIMISED=1,HGVSc=ENST00000592782.1:c.204C>T
CDS|ENST00000592782	VCF	synonymous_variant	341	341	0.0	.	.	AC_Male=6;AF_NFE=8.41548e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|2|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15518e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=3.50814e-05;Hom=0;AF_POPMAX=8.41548e-05;AN_POPMAX=83180;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|1|0|2|1|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=5.48296e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.21637e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.10980e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12023e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.28394e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:5.723e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001152,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000592782.1:c.210G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=3/13,ExAC_AMR_MAF=A:0,cDNA_position=341,CDS_position=210,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs369434915,VARIANT_CLASS=SNV,Protein_position=70,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:2.496e-05,HGVSc=ENST00000592782.1:c.210G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	353	353	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-83;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.48408e-06;Hom=0;AF_POPMAX=9.03506e-05;AN_POPMAX=11068;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=9.03506e-05;AC_raw=1;AB_MEDIAN=6.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.21150e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.96517e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.3e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=T:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=T:0.0002,Amino_acids=A,HGVSp=ENST00000592782.1:c.222C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/13,ExAC_AMR_MAF=T:0.0002112,cDNA_position=353,CDS_position=222,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs184508172,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=74,AA_MAF=T:0,Codons=gcC/gcT,MINIMISED=1,ExAC_AFR_MAF=T:8.398e-06,HGVSc=ENST00000592782.1:c.222C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	380	380	0.0	.	.	AC_Male=0;AF_NFE=9.11594e-06;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15014e-06;Hom=0;AF_POPMAX=9.11594e-06;AN_POPMAX=109698;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.77778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=9.19912e-06;GQ_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.62962e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.372e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.518e-05,AFR_MAF=C:0,SWISSPROT=P30419,EAS_MAF=C:0,EUR_MAF=C:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=C:0.0002,Amino_acids=S,HGVSp=ENST00000592782.1:c.249T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=4/13,ExAC_AMR_MAF=C:0,cDNA_position=380,CDS_position=249,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs200633656,SAS_MAF=C:0.001,VARIANT_CLASS=SNV,Protein_position=83,AA_MAF=C:0,Codons=tcT/tcC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.249T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	synonymous_variant	404	404	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|2|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22868e-05;Hom=0;AF_POPMAX=9.08045e-05;AN_POPMAX=33038;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46949e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=6.81818e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.81347e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.72461e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=9.08045e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000592782.1:c.273A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=4/13,cDNA_position=404,CDS_position=273,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=91,Codons=gaA/gaG,MINIMISED=1,HGVSc=ENST00000592782.1:c.273A>G
CDS|ENST00000592782	VCF	synonymous_variant	419	419	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-142;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07917e-06;Hom=0;AF_POPMAX=6.55996e-05;AN_POPMAX=15244;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=6.55996e-05;AC_raw=1;AB_MEDIAN=4.83146e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.02657e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.95139e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.272e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=C:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=I,HGVSp=ENST00000592782.1:c.288T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,EA_MAF=C:0.0002,Allele=C,IMPACT=LOW,EXON=4/13,ExAC_AMR_MAF=C:9.641e-05,cDNA_position=419,CDS_position=288,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs372318247,VARIANT_CLASS=SNV,Protein_position=96,Codons=atT/atC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.288T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	synonymous_variant	425	425	0.0	.	.	AC_Male=1;AF_NFE=8.97747e-06;Hom_FIN=0;GQ_MEDIAN=73;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97611e-06;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14538e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.54779e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.00868e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.44770e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.266e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.294G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/13,ExAC_AMR_MAF=T:0,cDNA_position=425,CDS_position=294,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754577624,VARIANT_CLASS=SNV,Protein_position=98,Codons=ctG/ctT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.294G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	431	431	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07193e-06;Hom=0;AF_POPMAX=3.25457e-05;AN_POPMAX=30726;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43141e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25457e-05;AS_RF=8.52320e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.300A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=4/13,cDNA_position=431,CDS_position=300,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=100,Codons=tcA/tcG,MINIMISED=1,HGVSc=ENST00000592782.1:c.300A>G
CDS|ENST00000592782	VCF	synonymous_variant	443	443	0.0	.	.	AC_Male=1;AF_NFE=8.99006e-06;Hom_FIN=0;GQ_MEDIAN=34;AB_HIST_ALT=0|0|0|0|4|3|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=4.08532e-04;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=1.35404e-04;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44760e-05;Hom=0;AF_POPMAX=1.35404e-04;AN_POPMAX=22156;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.44114e-06;AF_AFR=1.31406e-04;AC_raw=8;AB_MEDIAN=2.47642e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=4.51467e-05;GQ_HIST_ALT=0|1|1|0|0|1|1|1|0|0|1|0|1|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.54316e-03;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:6.621e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:6.02e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.312A>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=4/13,ExAC_AMR_MAF=C:0.0002899,cDNA_position=443,CDS_position=312,ExAC_NFE_MAF=C:0.0001537,SYMBOL=NMT1,Existing_variation=rs746348189,VARIANT_CLASS=SNV,Protein_position=104,Codons=ggA/ggC,MINIMISED=1,ExAC_AFR_MAF=C:9.060e-05,HGVSc=ENST00000592782.1:c.312A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	synonymous_variant	449	449	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07701e-06;Hom=0;AF_POPMAX=3.25945e-05;AN_POPMAX=30680;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25945e-05;AS_RF=8.53172e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592782.1:c.318C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/13,cDNA_position=449,CDS_position=318,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=106,Codons=gcC/gcT,MINIMISED=1,HGVSc=ENST00000592782.1:c.318C>T
CDS|ENST00000592782	VCF	synonymous_variant	467	467	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-42;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07501e-06;Hom=0;AF_POPMAX=2.99419e-05;AN_POPMAX=33398;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43450e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.92593e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.81783e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99419e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592782.1:c.336T>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=4/13,cDNA_position=467,CDS_position=336,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=112,Codons=gcT/gcC,MINIMISED=1,HGVSc=ENST00000592782.1:c.336T>C
CDS|ENST00000592782	VCF	synonymous_variant	470	470	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07465e-06;Hom=0;AF_POPMAX=2.99455e-05;AN_POPMAX=33394;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.67568e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=37;AF_Female=9.01518e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92008e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99455e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.339C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/13,cDNA_position=470,CDS_position=339,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=113,Codons=agC/agT,MINIMISED=1,HGVSc=ENST00000592782.1:c.339C>T
CDS|ENST00000592782	VCF	synonymous_variant	488	488	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=25;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15231e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=8;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66799e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000592782.1:c.357C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/13,cDNA_position=488,CDS_position=357,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=119,Codons=ttC/ttT,MINIMISED=1,HGVSc=ENST00000592782.1:c.357C>T
CDS|ENST00000592782	VCF	synonymous_variant	497	497	0.0	.	.	AC_Male=0;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-30;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.78261e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=9.08364e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.39564e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.366G>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/13,cDNA_position=497,CDS_position=366,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=122,Codons=acG/acT,HGVSc=ENST00000592782.1:c.366G>T
CDS|ENST00000592782	VCF	synonymous_variant	497	497	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|1|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.69441e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=3.02810e-05;AN_POPMAX=33024;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|3|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48671e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=1.60256e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.95538e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=3.02810e-05;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.366G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=4/13,cDNA_position=497,CDS_position=366,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=122,Codons=acG/acA,HGVSc=ENST00000592782.1:c.366G>A
CDS|ENST00000592782	VCF	synonymous_variant	503	503	0.0	.	.	AC_Male=13;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|2|0|5|2|0|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=15;Hom_NFE=0;AF=6.19001e-05;Hom=0;AF_POPMAX=4.28788e-04;AN_POPMAX=30318;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|4|2|1|1|1|0|1|0|0|2|1|0|0|1|0|0;AF_Male=9.78076e-05;AF_AFR=6.60153e-05;AC_raw=15;AB_MEDIAN=4.72797e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.82795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|15;Hom_raw=0;AF_SAS=4.28788e-04;AS_RF=9.33794e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.89692e-05;AC_SAS=13;POPMAX=SAS;AC_POPMAX=13;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09088e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.385e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0005311,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.372C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/13,ExAC_AMR_MAF=T:9.632e-05,cDNA_position=503,CDS_position=372,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs774578466,VARIANT_CLASS=SNV,Protein_position=124,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-05,HGVSc=ENST00000592782.1:c.372C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	509	509	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-31;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13839e-06;Hom=0;AF_POPMAX=3.31279e-05;AN_POPMAX=30186;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.54523e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.58333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.31279e-05;AS_RF=8.33412e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.422e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.378C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=4/13,ExAC_AMR_MAF=G:0,cDNA_position=509,CDS_position=378,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767261647,VARIANT_CLASS=SNV,Protein_position=126,Codons=ccC/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.378C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	530	530	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06669e-06;Hom=0;AF_POPMAX=3.24971e-05;AN_POPMAX=30772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42501e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24971e-05;AS_RF=9.28048e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.289e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592782.1:c.399C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=T:0,cDNA_position=530,CDS_position=399,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs760391896,VARIANT_CLASS=SNV,Protein_position=133,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000592782.1:c.399C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	533	533	0.0	.	.	AC_Male=1;AF_NFE=8.97054e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-32;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06544e-06;Hom=0;AF_POPMAX=8.97054e-06;AN_POPMAX=111476;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.48276e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.93308e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.285e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.508e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.402C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=A:0,cDNA_position=533,CDS_position=402,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs766241230,VARIANT_CLASS=SNV,Protein_position=134,Codons=acC/acA,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592782.1:c.402C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	539	539	0.0	.	.	AC_Male=0;AF_NFE=8.97022e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-93;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06521e-06;Hom=0;AF_POPMAX=8.97022e-06;AN_POPMAX=111480;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.90164e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98779e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40909e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.408C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/13,cDNA_position=539,CDS_position=408,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=136,Codons=ggC/ggT,MINIMISED=1,HGVSc=ENST00000592782.1:c.408C>T
CDS|ENST00000592782	VCF	synonymous_variant	542	542	0.0	.	.	AC_Male=22;AF_NFE=2.68986e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|9|6|8|6|4|1|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.00000e-61;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=37;Hom_NFE=0;AF=1.50378e-04;Hom=0;AF_POPMAX=2.68986e-04;AN_POPMAX=111530;AC_NFE=30;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|6|3|4|4|5|5|3|2|0|2|3|0|0|0|0;AF_Male=1.63236e-04;AF_AFR=0.00000e+00;AC_raw=37;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=0.00000e+00;DP_MEDIAN=45;AF_Female=1.34805e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|37;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=30;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.50240e-04;Hom_Female=0;AF_AMR=1.78710e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0003,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.411C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,EA_MAF=G:0.0002,Allele=G,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=542,CDS_position=411,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,Protein_position=137,Codons=ccC/ccG,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000592782.1:c.411C>G,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000592782	VCF	synonymous_variant	542	542	0.0	.	.	AC_Male=4;AF_NFE=2.68986e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|3|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-59;AF_OTH=3.64830e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25142e-05;Hom=0;AF_POPMAX=1.30702e-04;AN_POPMAX=15302;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|1|1|2|2|0|0|0|0|0|0|0|0|0;AF_Male=2.96793e-05;AF_AFR=1.30702e-04;AC_raw=8;AB_MEDIAN=4.75384e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.59479e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=2;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0003,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.411C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,EA_MAF=G:0.0002,Allele=T,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=542,CDS_position=411,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,Protein_position=137,Codons=ccC/ccT,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000592782.1:c.411C>T,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000592782	VCF	synonymous_variant	554	554	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06329e-06;Hom=0;AF_POPMAX=5.79845e-05;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53191e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50090e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79845e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.261e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0,EUR_MAF=T:0.001,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0.0001157,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=T:0.0002,Amino_acids=D,HGVSp=ENST00000592782.1:c.423C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=T:0,cDNA_position=554,CDS_position=423,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs535242567,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=141,AA_MAF=T:0,Codons=gaC/gaT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.423C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	557	557	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-50;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06339e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41851e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43104e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=K,HGVSp=ENST00000592782.1:c.426G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=5/13,cDNA_position=557,CDS_position=426,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=142,Codons=aaG/aaA,MINIMISED=1,HGVSc=ENST00000592782.1:c.426G>A
CDS|ENST00000592782	VCF	synonymous_variant	602	602	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|0|1|2|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-64;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84465e-05;Hom=0;AF_POPMAX=2.08445e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|0|1|0|2|0|1|0|0|1|0|0;AF_Male=1.48372e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=7;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=4.49317e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84239e-05;Hom_Female=0;AF_AMR=2.08445e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.65e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.471C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=G:0,cDNA_position=602,CDS_position=471,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs559376009,VARIANT_CLASS=SNV,Protein_position=157,Codons=acC/acG,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.471C>G,ExAC_Adj_MAF=G:0.0001732
CDS|ENST00000592782	VCF	synonymous_variant	618	618	0.0	.	.	AC_Male=25006;AF_NFE=2.09922e-01;Hom_FIN=285;GQ_MEDIAN=99;AB_HIST_ALT=0|0|5|15|72|453|1543|3857|7281|7755|7846|3986|1826|582|145|27|12|4|3|0;AC_FIN=3550;DREF_MEDIAN=1.00000e-73;AF_OTH=1.77555e-01;alleles=C%2CT;AF_FIN=1.59379e-01;AC_OTH=973;Hom_Male=2665;AC=45042;Hom_NFE=2465;AF=1.83181e-01;Hom=4839;AF_POPMAX=3.36036e-01;AN_POPMAX=15296;AC_NFE=23384;AS_FilterStatus=PASS;Hom_OTH=97;DP_HIST_ALT=2|26|94|195|538|1305|2559|3767|4480|4660|4316|3950|3356|2703|2157|1571|1256|914|624|548;AF_Male=1.85675e-01;AF_AFR=3.36036e-01;AC_raw=45128;AB_MEDIAN=4.75610e-01;Hom_EAS=11;AC_AMR=2943;AF_ASJ=1.65819e-01;DP_MEDIAN=52;AF_Female=1.80160e-01;GQ_HIST_ALT=6|6|7|9|6|14|13|17|10|21|33|20|43|66|53|88|83|83|130|39562;Hom_raw=4858;AF_SAS=2.21782e-01;AS_RF=9.54732e-01;Hom_AMR=167;AC_EAS=595;AC_Female=20036;Hom_AFR=875;Hom_ASJ=130;AF_EAS=3.44968e-02;AC_SAS=6826;POPMAX=AFR;AC_POPMAX=5140;AC_AFR=5140;Hom_SAS=809;AC_ASJ=1631;AF_raw=1.83246e-01;Hom_Female=2174;AF_AMR=8.76362e-02;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=T:0.3616,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=T:0.134,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=synonymous_variant,GMAF=T:0.1991,ExAC_SAS_MAF=T:0.1752,SOMATIC=0&1,IMPACT=LOW,ExAC_AMR_MAF=T:0.3348,CDS_position=487,ExAC_NFE_MAF=T:0.1553,SYMBOL=NMT1,Existing_variation=rs1132898&COSM3755586,VARIANT_CLASS=SNV,Protein_position=163,AA_MAF=T:0.2157,Codons=Ctg/Ttg,ExAC_Adj_MAF=T:0.08946,PHENO=0&1,ExAC_EAS_MAF=T:0.1935,ExAC_MAF=T:0.2031,BIOTYPE=protein_coding,ExAC_OTH_MAF=T:0.2069,AFR_MAF=T:0.2226,SWISSPROT=P30419,EUR_MAF=T:0.0367,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,ExAC_FIN_MAF=T:0.0346,ENSP=ENSP00000468424,Amino_acids=L,HGVSp=ENST00000592782.1:c.487C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,EA_MAF=T:0.325,Allele=T,EXON=5/13,cDNA_position=618,SAS_MAF=T:0.1769,MINIMISED=1,ExAC_AFR_MAF=T:0.193,HGVSc=ENST00000592782.1:c.487C>T
CDS|ENST00000592782	VCF	synonymous_variant	620	620	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-69;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06557e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.42280e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.31034e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=8.87045e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.489G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=5/13,cDNA_position=620,CDS_position=489,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=163,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000592782.1:c.489G>A
CDS|ENST00000592782	VCF	synonymous_variant	623	623	0.0	.	.	AC_Male=2;AF_NFE=1.79498e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|2|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-46;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21991e-05;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|1;AF_Male=1.48469e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.69796e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=8.99184e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.10458e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.652e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.006e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.492C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=T:0,cDNA_position=623,CDS_position=492,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749766632,VARIANT_CLASS=SNV,Protein_position=164,Codons=ggC/ggT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.492C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	629	629	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-64;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06901e-06;Hom=0;AF_POPMAX=6.53595e-05;AN_POPMAX=15300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53595e-05;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=8.99653e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.86417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000592782.1:c.498T>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=5/13,cDNA_position=629,CDS_position=498,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=166,Codons=cgT/cgG,MINIMISED=1,HGVSc=ENST00000592782.1:c.498T>G
CDS|ENST00000592782	VCF	synonymous_variant	632	632	0.0	.	.	AC_Male=0;AF_NFE=8.98537e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-29;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06891e-06;Hom=0;AF_POPMAX=8.98537e-06;AN_POPMAX=111292;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.11111e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=18;AF_Female=8.99491e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.57047e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.267e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.503e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.501T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=C:0,cDNA_position=632,CDS_position=501,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs772281237,VARIANT_CLASS=SNV,Protein_position=167,Codons=ggT/ggC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.501T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	synonymous_variant	653	653	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|2|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16108e-109;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.24865e-05;Hom=0;AF_POPMAX=2.38223e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|3|0|0|0|0|0|1|1;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.25397e-01;Hom_EAS=0;AC_AMR=8;AF_ASJ=0.00000e+00;DP_MEDIAN=93;AF_Female=5.38812e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=6;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=8;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=2.38223e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:3.295e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.522C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=6/13,ExAC_AMR_MAF=T:0,cDNA_position=653,CDS_position=522,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs770678984,VARIANT_CLASS=SNV,Protein_position=174,Codons=acC/acT,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000592782.1:c.522C>T,ExAC_Adj_MAF=T:0.0003455
CDS|ENST00000592782	VCF	synonymous_variant	686	686	0.0	.	.	AC_Male=4;AF_NFE=5.37095e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-123;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43643e-05;Hom=0;AF_POPMAX=5.37095e-05;AN_POPMAX=111712;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|1;AF_Male=2.96512e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.30292e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=135;AF_Female=1.79598e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.942e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.991e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000592782.1:c.555C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=6/13,ExAC_AMR_MAF=T:0,cDNA_position=686,CDS_position=555,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs776474941,VARIANT_CLASS=SNV,Protein_position=185,Codons=gaC/gaT,MINIMISED=1,ExAC_AFR_MAF=T:4.942e-05,HGVSc=ENST00000592782.1:c.555C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	689	689	0.0	.	.	AC_Male=0;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-101;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.05660e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=106;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12871e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592782.1:c.558C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=6/13,cDNA_position=689,CDS_position=558,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=186,Codons=aaC/aaT,MINIMISED=1,HGVSc=ENST00000592782.1:c.558C>T
CDS|ENST00000592782	VCF	synonymous_variant	701	701	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-132;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.34426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=122;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.50786e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000592782.1:c.570T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=6/13,ExAC_AMR_MAF=C:0,cDNA_position=701,CDS_position=570,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs759459614,VARIANT_CLASS=SNV,Protein_position=190,Codons=ttT/ttC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.570T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	synonymous_variant	710	710	0.0	.	.	AC_Male=4;AF_NFE=1.16371e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|3|5|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-93;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=13;Hom_NFE=0;AF=5.27897e-05;Hom=0;AF_POPMAX=1.16371e-04;AN_POPMAX=111712;AC_NFE=13;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|2|1|1|0|0|1|0|0|1;AF_Male=2.96507e-05;AF_AFR=0.00000e+00;AC_raw=13;AB_MEDIAN=4.05405e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=97;AF_Female=8.08219e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|13;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.28067e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=13;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.27872e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:6.589e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001199,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.579C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=6/13,ExAC_AMR_MAF=A:0,cDNA_position=710,CDS_position=579,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs372926712,VARIANT_CLASS=SNV,Protein_position=193,Codons=tcC/tcA,MINIMISED=1,ExAC_AFR_MAF=A:6.589e-05,HGVSc=ENST00000592782.1:c.579C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	713	713	0.0	.	.	AC_Male=380;AF_NFE=2.32750e-03;Hom_FIN=3;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|2|40|88|203|202|119|49|4|0|0|0|0|0|0|0;AC_FIN=293;DREF_MEDIAN=5.01187e-117;AF_OTH=3.83072e-03;alleles=G%2CA;AF_FIN=1.31390e-02;AC_OTH=21;Hom_Male=2;AC=716;Hom_NFE=0;AF=2.90754e-03;Hom=4;AF_POPMAX=1.31390e-02;AN_POPMAX=22300;AC_NFE=260;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|5|6|15|17|25|30|39|50|52|47|44|38|56;AF_Male=2.81686e-03;AF_AFR=2.61370e-04;AC_raw=716;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=45;AF_ASJ=9.23858e-03;DP_MEDIAN=93;AF_Female=3.01740e-03;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|712;Hom_raw=4;AF_SAS=3.24865e-05;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=1;AC_Female=336;Hom_AFR=0;Hom_ASJ=1;AF_EAS=5.79777e-05;AC_SAS=1;POPMAX=FIN;AC_POPMAX=293;AC_AFR=4;Hom_SAS=0;AC_ASJ=91;AF_raw=2.90735e-03;Hom_Female=2;AF_AMR=1.34000e-03;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.002586,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0022,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=A:0.0004,Amino_acids=P,HGVSp=ENST00000592782.1:c.582G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0.003311,CCDS=CCDS11494.1,EA_MAF=A:0.0005,Allele=A,IMPACT=LOW,EXON=6/13,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=713,CDS_position=582,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,Protein_position=194,AA_MAF=A:0,Codons=ccG/ccA,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000592782.1:c.582G>A,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000592782	VCF	synonymous_variant	713	713	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-124;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.71429e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41835e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.002586,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0022,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=A:0.0004,Amino_acids=P,HGVSp=ENST00000592782.1:c.582G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0.003311,CCDS=CCDS11494.1,EA_MAF=A:0.0005,Allele=T,IMPACT=LOW,EXON=6/13,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=713,CDS_position=582,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,Protein_position=194,AA_MAF=A:0,Codons=ccG/ccT,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000592782.1:c.582G>T,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000592782	VCF	synonymous_variant	743	743	0.0	.	.	AC_Male=4;AF_NFE=5.37577e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00079e-202;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43754e-05;Hom=0;AF_POPMAX=5.37577e-05;AN_POPMAX=111612;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|1;AF_Male=2.96630e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=5.20944e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=152;AF_Female=1.79691e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35748e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.612C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=7/13,ExAC_AMR_MAF=T:0,cDNA_position=743,CDS_position=612,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757227703&COSM4130155,VARIANT_CLASS=SNV,Protein_position=204,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000592782.1:c.612C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	770	770	0.0	.	.	AC_Male=1;AF_NFE=1.79045e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-65;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12163e-06;Hom=0;AF_POPMAX=1.79045e-05;AN_POPMAX=111704;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.08500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=57;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.42948e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.639G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=7/13,ExAC_AMR_MAF=A:0,cDNA_position=770,CDS_position=639,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768715452,VARIANT_CLASS=SNV,Protein_position=213,Codons=ggG/ggA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.639G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	782	782	0.0	.	.	AC_Male=9;AF_NFE=2.32741e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|11|10|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-104;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=26;Hom_NFE=0;AF=1.05578e-04;Hom=0;AF_POPMAX=2.32741e-04;AN_POPMAX=111712;AC_NFE=26;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|3|0|2|5|0|2;AF_Male=6.67141e-05;AF_AFR=0.00000e+00;AC_raw=26;AB_MEDIAN=4.45780e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=98;AF_Female=1.52658e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|26;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=17;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=26;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.05574e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.885e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0003,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001798,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000592782.1:c.651C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=7/13,ExAC_AMR_MAF=T:0,cDNA_position=782,CDS_position=651,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs199671891,VARIANT_CLASS=SNV,Protein_position=217,Codons=gtC/gtT,MINIMISED=1,ExAC_AFR_MAF=T:9.884e-05,HGVSc=ENST00000592782.1:c.651C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	791	791	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-154;AF_OTH=1.82282e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.60938e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000592782.1:c.660G>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=7/13,cDNA_position=791,CDS_position=660,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=220,Codons=cgG/cgC,MINIMISED=1,HGVSc=ENST00000592782.1:c.660G>C
CDS|ENST00000592782	VCF	synonymous_variant	812	812	0.0	.	.	AC_Male=2;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21823e-05;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=1.48249e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.91803e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.01565e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.647e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.681C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=7/13,ExAC_AMR_MAF=T:0,cDNA_position=812,CDS_position=681,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772957252,VARIANT_CLASS=SNV,Protein_position=227,Codons=agC/agT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.681C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	821	821	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-140;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.49153e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=118;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.690A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=7/13,ExAC_AMR_MAF=G:0,cDNA_position=821,CDS_position=690,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs770200317,VARIANT_CLASS=SNV,Protein_position=230,Codons=ccA/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.690A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	839	839	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-84;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06138e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.92754e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=69;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.86417e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=Y,HGVSp=ENST00000592782.1:c.708T>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=7/13,cDNA_position=839,CDS_position=708,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=236,Codons=taT/taC,MINIMISED=1,HGVSc=ENST00000592782.1:c.708T>C
CDS|ENST00000592782	VCF	synonymous_variant	893	893	0.0	.	.	AC_Male=1;AF_NFE=8.95367e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-83;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06121e-06;Hom=0;AF_POPMAX=8.95367e-06;AN_POPMAX=111686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41400e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.37037e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.49406e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.762G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=8/13,cDNA_position=893,CDS_position=762,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=254,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000592782.1:c.762G>A
CDS|ENST00000592782	VCF	synonymous_variant	899	899	0.0	.	.	AC_Male=2;AF_NFE=2.68562e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-156;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21825e-05;Hom=0;AF_POPMAX=2.68562e-05;AN_POPMAX=111706;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0;AF_Male=1.48265e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.28302e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33696e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.768C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=T:0,cDNA_position=899,CDS_position=768,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs770379933,VARIANT_CLASS=SNV,Protein_position=256,Codons=tcC/tcT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.768C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	905	905	0.0	.	.	AC_Male=7;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|3|5|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-120;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.46675e-05;Hom=0;AF_POPMAX=3.24865e-04;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|2|1|2|0|0|0|0|1|1;AF_Male=5.18880e-05;AF_AFR=6.53424e-05;AC_raw=11;AB_MEDIAN=4.69613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=92;AF_Female=3.59202e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=3.24865e-04;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=10;POPMAX=SAS;AC_POPMAX=10;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:5.766e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0003634,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000592782.1:c.774G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=905,CDS_position=774,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs780855060,VARIANT_CLASS=SNV,Protein_position=258,Codons=agG/agA,MINIMISED=1,ExAC_AFR_MAF=A:5.765e-05,HGVSc=ENST00000592782.1:c.774G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	929	929	0.0	.	.	AC_Male=23;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|8|24|20|21|5|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.07688e-127;AF_OTH=1.82349e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=85;Hom_NFE=0;AF=3.45164e-04;Hom=1;AF_POPMAX=3.98589e-03;AN_POPMAX=15304;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|2|4|1|6|4|3|5|6|3|1|3|5;AF_Male=1.70492e-04;AF_AFR=3.98589e-03;AC_raw=85;AB_MEDIAN=4.72222e-01;Hom_EAS=0;AC_AMR=19;AF_ASJ=3.04569e-04;DP_MEDIAN=97;AF_Female=5.56773e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|84;Hom_raw=1;AF_SAS=3.24865e-05;AS_RF=9.53297e-01;Hom_AMR=0;AC_EAS=0;AC_Female=62;Hom_AFR=1;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=61;AC_AFR=61;Hom_SAS=0;AC_ASJ=3;AF_raw=3.45147e-04;Hom_Female=1;AF_AMR=5.65779e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.0004366,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0002,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0.0061,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=A:0.0016,Amino_acids=E,HGVSp=ENST00000592782.1:c.798G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0.001101,CCDS=CCDS11494.1,EA_MAF=A:0.0052,Allele=A,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=A:0.004228,cDNA_position=929,CDS_position=798,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs146578323,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=266,AA_MAF=A:0,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:4.365e-04,HGVSc=ENST00000592782.1:c.798G>A,ExAC_Adj_MAF=A:0.0005183
CDS|ENST00000592782	VCF	synonymous_variant	935	935	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-30;AF_OTH=1.82349e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=8.98037e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.72787e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.804C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=8/13,cDNA_position=935,CDS_position=804,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=268,Codons=acC/acT,MINIMISED=1,HGVSc=ENST00000592782.1:c.804C>T
CDS|ENST00000592782	VCF	synonymous_variant	950	950	0.0	.	.	AC_Male=15;AF_NFE=3.58153e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|5|5|3|5|3|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-69;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=25;Hom_NFE=0;AF=1.01531e-04;Hom=0;AF_POPMAX=1.11082e-03;AN_POPMAX=15304;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|1|1|2|4|5|1|1|1|2|0|1|0;AF_Male=1.11200e-04;AF_AFR=1.11082e-03;AC_raw=25;AB_MEDIAN=4.82014e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98166e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|25;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.93009e-01;Hom_AMR=0;AC_EAS=0;AC_Female=10;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=17;AC_AFR=17;Hom_SAS=0;AC_ASJ=0;AF_raw=1.01514e-04;Hom_Female=0;AF_AMR=1.19111e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:4.943e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=A:0.0002,Amino_acids=L,HGVSp=ENST00000592782.1:c.819G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0005,Allele=A,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=A:0.0003844,cDNA_position=950,CDS_position=819,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs201216212,SAS_MAF=A:0.001,VARIANT_CLASS=SNV,Protein_position=273,AA_MAF=A:0,Codons=ctG/ctA,MINIMISED=1,ExAC_AFR_MAF=A:4.942e-05,HGVSc=ENST00000592782.1:c.819G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	962	962	0.0	.	.	AC_Male=1;AF_NFE=8.95383e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-154;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06128e-06;Hom=0;AF_POPMAX=8.95383e-06;AN_POPMAX=111684;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41345e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=115;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000592782.1:c.831C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=T:0,cDNA_position=962,CDS_position=831,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766086965,VARIANT_CLASS=SNV,Protein_position=277,Codons=ttC/ttT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.831C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	980	980	0.0	.	.	AC_Male=3;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|1|1|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-112;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43815e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|1|2|0|1;AF_Male=2.22499e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.63415e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=87;AF_Female=2.69648e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=4;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=1;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.24e-06&T:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0&T:0.0003467,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592782.1:c.849C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=A:0&T:0,cDNA_position=980,CDS_position=849,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs773804544,VARIANT_CLASS=SNV,Protein_position=283,Codons=gcC/gcT,ExAC_AFR_MAF=A:8.236e-06&T:3.295e-05,HGVSc=ENST00000592782.1:c.849C>T,ExAC_Adj_MAF=A:0&T:0
CDS|ENST00000592782	VCF	synonymous_variant	980	980	0.0	.	.	AC_Male=1;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-101;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06359e-06;Hom=0;AF_POPMAX=8.96379e-06;AN_POPMAX=111560;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.41664e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=84;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.24e-06&T:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0&T:0.0003467,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592782.1:c.849C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=A:0&T:0,cDNA_position=980,CDS_position=849,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs773804544,VARIANT_CLASS=SNV,Protein_position=283,Codons=gcC/gcA,ExAC_AFR_MAF=A:8.236e-06&T:3.295e-05,HGVSc=ENST00000592782.1:c.849C>A,ExAC_Adj_MAF=A:0&T:0
CDS|ENST00000592782	VCF	synonymous_variant	983	983	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-131;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06342e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41675e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.35644e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=101;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.45417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.241e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.852G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=T:0,cDNA_position=983,CDS_position=852,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs777042262,VARIANT_CLASS=SNV,Protein_position=284,Codons=ggG/ggT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.852G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	992	992	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|2|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38770e-91;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03277e-05;Hom=0;AF_POPMAX=2.89922e-04;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|1|0|1|1|1|0|0;AF_Male=2.22605e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.67647e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=1.79853e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43239e-01;Hom_AMR=0;AC_EAS=5;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.89922e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:3.298e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0.0004622,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.861A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=G:0,cDNA_position=992,CDS_position=861,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs765144876,VARIANT_CLASS=SNV,Protein_position=287,Codons=ctA/ctG,MINIMISED=1,ExAC_AFR_MAF=G:3.295e-05,HGVSc=ENST00000592782.1:c.861A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	995	995	0.0	.	.	AC_Male=1;AF_NFE=8.97876e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-116;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06693e-06;Hom=0;AF_POPMAX=8.97876e-06;AN_POPMAX=111374;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.42269e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.18519e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=81;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.07420e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=1,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.864A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,SOMATIC=1,Allele=G,IMPACT=LOW,EXON=8/13,cDNA_position=995,CDS_position=864,SYMBOL=NMT1,Existing_variation=COSM980092,VARIANT_CLASS=SNV,Protein_position=288,Codons=ccA/ccG,MINIMISED=1,HGVSc=ENST00000592782.1:c.864A>G
CDS|ENST00000592782	VCF	synonymous_variant	1001	1001	0.0	.	.	AC_Male=16886;AF_NFE=7.81798e-02;Hom_FIN=144;GQ_MEDIAN=99;AB_HIST_ALT=0|0|4|11|34|169|815|2369|5579|6526|6364|2859|1315|395|126|40|13|6|2|0;AC_FIN=2671;DREF_MEDIAN=1.58489e-82;AF_OTH=1.21898e-01;alleles=C%2CT;AF_FIN=1.19862e-01;AC_OTH=668;Hom_Male=1379;AC=32227;Hom_NFE=374;AF=1.31220e-01;Hom=2825;AF_POPMAX=2.70280e-01;AN_POPMAX=17234;AC_NFE=8690;AS_FilterStatus=PASS;Hom_OTH=38;DP_HIST_ALT=0|34|152|543|1210|1834|1980|1919|2086|2037|2144|2084|2059|2011|1891|1563|1322|1089|843|766;AF_Male=1.25481e-01;AF_AFR=1.64684e-01;AC_raw=32293;AB_MEDIAN=4.80000e-01;Hom_EAS=624;AC_AMR=8200;AF_ASJ=1.11156e-01;DP_MEDIAN=56;AF_Female=1.38175e-01;GQ_HIST_ALT=2|5|5|5|6|4|15|8|13|29|37|35|59|87|46|89|130|54|99|28732;Hom_raw=2833;AF_SAS=1.21133e-01;AS_RF=9.54732e-01;Hom_AMR=1132;AC_EAS=4658;AC_Female=15341;Hom_AFR=203;Hom_ASJ=67;AF_EAS=2.70280e-01;AC_SAS=3728;POPMAX=EAS;AC_POPMAX=4658;AC_AFR=2520;Hom_SAS=243;AC_ASJ=1092;AF_raw=1.31127e-01;Hom_Female=1446;AF_AMR=2.44470e-01;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=T:0.1717,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=T:0.2003,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=synonymous_variant,GMAF=T:0.1707,ExAC_SAS_MAF=T:0.1082,SOMATIC=0&1,IMPACT=LOW,ExAC_AMR_MAF=T:0.1637,CDS_position=870,ExAC_NFE_MAF=T:0.1181,SYMBOL=NMT1,Existing_variation=rs2239922&COSM4130156,VARIANT_CLASS=SNV,Protein_position=290,AA_MAF=T:0.138,Codons=ccC/ccT,ExAC_Adj_MAF=T:0.2522,PHENO=0&1,ExAC_EAS_MAF=T:0.1255,ExAC_MAF=T:0.084,BIOTYPE=protein_coding,ExAC_OTH_MAF=T:0.08058,AFR_MAF=T:0.1247,SWISSPROT=P30419,EUR_MAF=T:0.2669,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,ExAC_FIN_MAF=T:0.2664,ENSP=ENSP00000468424,Amino_acids=P,HGVSp=ENST00000592782.1:c.870C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,EA_MAF=T:0.1609,Allele=T,EXON=8/13,cDNA_position=1001,SAS_MAF=T:0.0845,MINIMISED=1,ExAC_AFR_MAF=T:0.125,HGVSc=ENST00000592782.1:c.870C>T
CDS|ENST00000592782	VCF	synonymous_variant	1010	1010	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-66;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07485e-06;Hom=0;AF_POPMAX=3.24971e-05;AN_POPMAX=30772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43837e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24971e-05;AS_RF=9.36271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.879C>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=8/13,cDNA_position=1010,CDS_position=879,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=293,Codons=acC/acG,MINIMISED=1,HGVSc=ENST00000592782.1:c.879C>G
CDS|ENST00000592782	VCF	synonymous_variant	1047	1047	0.0	.	.	AC_Male=35456;AF_NFE=2.86445e-01;Hom_FIN=602;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|5|45|265|1612|6264|14024|13853|7316|1836|403|56|20|5|1|7|0|0;AC_FIN=5122;DREF_MEDIAN=5.01187e-129;AF_OTH=2.67688e-01;alleles=C%2CT;AF_FIN=2.29686e-01;AC_OTH=1468;Hom_Male=4900;AC=62473;Hom_NFE=4541;AF=2.53714e-01;Hom=8385;AF_POPMAX=3.13873e-01;AN_POPMAX=30780;AC_NFE=31993;AS_FilterStatus=PASS;Hom_OTH=200;DP_HIST_ALT=0|4|10|40|98|183|365|643|1031|1413|1780|2104|2153|2372|2313|2427|2475|2656|2744|3260;AF_Male=2.62863e-01;AF_AFR=8.24621e-02;AC_raw=62491;AB_MEDIAN=4.51613e-01;Hom_EAS=523;AC_AMR=5860;AF_ASJ=2.83046e-01;DP_MEDIAN=99;AF_Female=2.42631e-01;GQ_HIST_ALT=1|1|1|3|5|1|2|2|7|5|3|7|10|13|9|10|20|17|27|53958;Hom_raw=8389;AF_SAS=3.13873e-01;AS_RF=9.54732e-01;Hom_AMR=536;AC_EAS=4319;AC_Female=27017;Hom_AFR=44;Hom_ASJ=372;AF_EAS=2.50435e-01;AC_SAS=9661;POPMAX=SAS;AC_POPMAX=9661;AC_AFR=1262;Hom_SAS=1567;AC_ASJ=2788;AF_raw=2.53748e-01;Hom_Female=3485;AF_AMR=1.74509e-01;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=T:0.059,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=T:0.2017,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=synonymous_variant,GMAF=T:0.2240,ExAC_SAS_MAF=T:0.2671,SOMATIC=0&1,IMPACT=LOW,ExAC_AMR_MAF=T:0.08428,CDS_position=916,ExAC_NFE_MAF=T:0.2272,SYMBOL=NMT1,Existing_variation=rs2239923&COSM4000177,VARIANT_CLASS=SNV,Protein_position=306,AA_MAF=T:0.3333,Codons=Ctg/Ttg,ExAC_Adj_MAF=T:0.1691,PHENO=0&1,ExAC_EAS_MAF=T:0.2516,ExAC_MAF=T:0.2892,BIOTYPE=protein_coding,ExAC_OTH_MAF=T:0.2796,AFR_MAF=T:0.3133,SWISSPROT=P30419,EUR_MAF=T:0.2748,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,ExAC_FIN_MAF=T:0.2472,ENSP=ENSP00000468424,Amino_acids=L,HGVSp=ENST00000592782.1:c.916C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,EA_MAF=T:0.0921,Allele=T,EXON=9/13,cDNA_position=1047,SAS_MAF=T:0.2992,MINIMISED=1,ExAC_AFR_MAF=T:0.252,HGVSc=ENST00000592782.1:c.916C>T
CDS|ENST00000592782	VCF	synonymous_variant	1052	1052	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-115;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57447e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.07652e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=I,HGVSp=ENST00000592782.1:c.921T>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=9/13,cDNA_position=1052,CDS_position=921,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=307,Codons=atT/atC,MINIMISED=1,HGVSc=ENST00000592782.1:c.921T>C
CDS|ENST00000592782	VCF	synonymous_variant	1058	1058	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-265;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.84211e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=190;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.26718e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000592782.1:c.927G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=9/13,ExAC_AMR_MAF=T:0,cDNA_position=1058,CDS_position=927,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs779600514,VARIANT_CLASS=SNV,Protein_position=309,Codons=gtG/gtT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.927G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1064	1064	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-52;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.25532e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.45417e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000592782.1:c.933C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=9/13,cDNA_position=1064,CDS_position=933,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=311,Codons=ttC/ttT,MINIMISED=1,HGVSc=ENST00000592782.1:c.933C>T
CDS|ENST00000592782	VCF	synonymous_variant	1073	1073	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-21;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.56863e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=102;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=4.74649e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.942G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=9/13,cDNA_position=1073,CDS_position=942,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=314,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000592782.1:c.942G>A
CDS|ENST00000592782	VCF	synonymous_variant	1109	1109	0.0	.	.	AC_Male=1;AF_NFE=8.96106e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-92;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06303e-06;Hom=0;AF_POPMAX=8.96106e-06;AN_POPMAX=111594;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41719e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.39683e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50841e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.978C>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=9/13,cDNA_position=1109,CDS_position=978,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=326,Codons=ctC/ctG,MINIMISED=1,HGVSc=ENST00000592782.1:c.978C>G
CDS|ENST00000592782	VCF	synonymous_variant	1115	1115	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-120;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06375e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=104;AF_Female=8.98666e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20293e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.244e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000592782.1:c.984A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=9/13,ExAC_AMR_MAF=G:0,cDNA_position=1115,CDS_position=984,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs748936607,VARIANT_CLASS=SNV,Protein_position=328,Codons=cgA/cgG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.984A>G,ExAC_Adj_MAF=G:8.645e-05
CDS|ENST00000592782	VCF	synonymous_variant	1145	1145	0.0	.	.	AC_Male=1;AF_NFE=8.96636e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06560e-06;Hom=0;AF_POPMAX=8.96636e-06;AN_POPMAX=111528;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42236e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.05405e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=37;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.73634e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.1014G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=10/13,cDNA_position=1145,CDS_position=1014,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=338,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000592782.1:c.1014G>A
CDS|ENST00000592782	VCF	synonymous_variant	1172	1172	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-112;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06134e-06;Hom=0;AF_POPMAX=2.97885e-05;AN_POPMAX=33570;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41367e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.22222e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=90;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97885e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.1041A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=10/13,cDNA_position=1172,CDS_position=1041,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=347,Codons=ccA/ccG,MINIMISED=1,HGVSc=ENST00000592782.1:c.1041A>G
CDS|ENST00000592782	VCF	synonymous_variant	1178	1178	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-82;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06124e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41334e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.27610e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000592782.1:c.1047G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=10/13,cDNA_position=1178,CDS_position=1047,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=349,Codons=gtG/gtA,MINIMISED=1,HGVSc=ENST00000592782.1:c.1047G>A
CDS|ENST00000592782	VCF	synonymous_variant	1193	1193	0.0	.	.	AC_Male=3;AF_NFE=8.95239e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|4|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94028e-59;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43661e-05;Hom=0;AF_POPMAX=1.48916e-04;AN_POPMAX=33576;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|1|2|0|1|1|0|0|0;AF_Male=2.22390e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=3.71530e-01;Hom_EAS=0;AC_AMR=5;AF_ASJ=0.00000e+00;DP_MEDIAN=67;AF_Female=2.69430e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.22228e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=1.48916e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.241e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.1062C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=10/13,ExAC_AMR_MAF=A:0,cDNA_position=1193,CDS_position=1062,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs751985902,VARIANT_CLASS=SNV,Protein_position=354,Codons=acC/acA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.1062C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	1196	1196	0.0	.	.	AC_Male=5;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|4|1|1|4|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-70;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.68519e-05;Hom=0;AF_POPMAX=4.16915e-04;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|1|1|2|1|1|3|1|1|1|0|0|0;AF_Male=3.70645e-05;AF_AFR=0.00000e+00;AC_raw=14;AB_MEDIAN=4.70918e-01;Hom_EAS=0;AC_AMR=14;AF_ASJ=0.00000e+00;DP_MEDIAN=59;AF_Female=8.08233e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=14;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.68477e-05;Hom_Female=0;AF_AMR=4.16915e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000592782.1:c.1065G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=10/13,ExAC_AMR_MAF=A:0,cDNA_position=1196,CDS_position=1065,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs781580851,VARIANT_CLASS=SNV,Protein_position=355,Codons=agG/agA,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000592782.1:c.1065G>A,ExAC_Adj_MAF=A:0.0003456
CDS|ENST00000592782	VCF	synonymous_variant	1223	1223	0.0	.	.	AC_Male=6;AF_NFE=3.58057e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|3|3|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-65;AF_OTH=1.82415e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.46701e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|3|0|0|1|1|1|0|0|0|0|2|0|0;AF_Male=4.44774e-05;AF_AFR=0.00000e+00;AC_raw=11;AB_MEDIAN=3.98148e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=62;AF_Female=4.49035e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=6.49773e-05;AS_RF=9.34832e-01;Hom_AMR=0;AC_EAS=4;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=2;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:6.591e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:5.996e-05,AFR_MAF=T:0.0001211,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0.0002311,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.1092C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/13,ExAC_AMR_MAF=T:0,cDNA_position=1223,CDS_position=1092,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs769815313,VARIANT_CLASS=SNV,Protein_position=364,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:6.589e-05,HGVSc=ENST00000592782.1:c.1092C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1262	1262	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-36;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12466e-06;Hom=0;AF_POPMAX=6.49857e-05;AN_POPMAX=30776;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41554e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.53526e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=8.98376e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.49857e-05;AS_RF=9.31176e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.251e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.1131C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=10/13,ExAC_AMR_MAF=G:0,cDNA_position=1262,CDS_position=1131,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs749581366,VARIANT_CLASS=SNV,Protein_position=377,Codons=ccC/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.1131C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	1265	1265	0.0	.	.	AC_Male=2;AF_NFE=1.79112e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-80;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12460e-06;Hom=0;AF_POPMAX=1.79112e-05;AN_POPMAX=111662;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0;AF_Male=1.48304e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.07843e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08567e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=Q,HGVSp=ENST00000592782.1:c.1134G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=10/13,cDNA_position=1265,CDS_position=1134,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=378,Codons=caG/caA,MINIMISED=1,HGVSc=ENST00000592782.1:c.1134G>A
CDS|ENST00000592782	VCF	synonymous_variant	1277	1277	0.0	.	.	AC_Male=0;AF_NFE=8.96572e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-50;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06570e-06;Hom=0;AF_POPMAX=8.96572e-06;AN_POPMAX=111536;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.20690e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=8.99103e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19671e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=I,HGVSp=ENST00000592782.1:c.1146C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/13,cDNA_position=1277,CDS_position=1146,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=382,Codons=atC/atT,MINIMISED=1,HGVSc=ENST00000592782.1:c.1146C>T
CDS|ENST00000592782	VCF	synonymous_variant	1286	1286	0.0	.	.	AC_Male=4;AF_NFE=8.96861e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97631e-68;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62689e-05;Hom=0;AF_POPMAX=1.73933e-04;AN_POPMAX=17248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=2.96969e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.51825e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=87;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.37116e-01;Hom_AMR=0;AC_EAS=3;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.73933e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:1.664e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.507e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000592782.1:c.1155C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=10/13,ExAC_AMR_MAF=T:0,cDNA_position=1286,CDS_position=1155,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs768875089&COSM980093,VARIANT_CLASS=SNV,Protein_position=385,Codons=ttC/ttT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.1155C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1292	1292	0.0	.	.	AC_Male=1;AF_NFE=8.97811e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-131;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07047e-06;Hom=0;AF_POPMAX=8.97811e-06;AN_POPMAX=111382;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.42986e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.39326e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33934e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.345e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.51e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000592782.1:c.1161G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=10/13,ExAC_AMR_MAF=A:0,cDNA_position=1292,CDS_position=1161,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs774502405,VARIANT_CLASS=SNV,Protein_position=387,Codons=gtG/gtA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.1161G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	1304	1304	0.0	.	.	AC_Male=1;AF_NFE=2.71444e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|3|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-100;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.45570e-05;Hom=0;AF_POPMAX=5.80114e-05;AN_POPMAX=17238;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|1|0|0|0|0|0|1|0|0|1|0|0|0;AF_Male=7.47664e-06;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.79833e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=73;AF_Female=4.52161e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=3.27804e-05;AS_RF=9.44920e-01;Hom_AMR=0;AC_EAS=1;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80114e-05;AC_SAS=1;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43635e-05;Hom_Female=0;AF_AMR=2.99312e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.528e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0002,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.03e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592782.1:c.1173C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1304,CDS_position=1173,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs369014766,VARIANT_CLASS=SNV,Protein_position=391,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000592782.1:c.1173C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1316	1316	0.0	.	.	AC_Male=3;AF_NFE=3.60529e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-44;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63157e-05;Hom=0;AF_POPMAX=3.60529e-05;AN_POPMAX=110948;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=2.23567e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.08621e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=59;AF_Female=9.01112e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05369e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.324e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.507e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.1185A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=G:0,cDNA_position=1316,CDS_position=1185,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs771817702,VARIANT_CLASS=SNV,Protein_position=395,Codons=acA/acG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.1185A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	1337	1337	0.0	.	.	AC_Male=4;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|1|0|4|2|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.58114e-48;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=4.48752e-05;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25698e-05;Hom=0;AF_POPMAX=2.28087e-04;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|1|1|0|0|0|0|0|1|1|0|0|0|0|0;AF_Male=2.97296e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.70158e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=52;AF_Female=3.60101e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=2.28087e-04;AS_RF=9.06358e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=7;POPMAX=SAS;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.476e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0001828,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.1206G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1337,CDS_position=1206,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746713731,VARIANT_CLASS=SNV,Protein_position=402,Codons=acG/acA,ExAC_AFR_MAF=A:2.471e-05,HGVSc=ENST00000592782.1:c.1206G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	1337	1337	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-28;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07123e-06;Hom=0;AF_POPMAX=3.25839e-05;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43240e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25839e-05;AS_RF=8.36271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.476e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0001828,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.1206G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1337,CDS_position=1206,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746713731,VARIANT_CLASS=SNV,Protein_position=402,Codons=acG/acT,ExAC_AFR_MAF=A:2.471e-05,HGVSc=ENST00000592782.1:c.1206G>T,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	1358	1358	0.0	.	.	AC_Male=1;AF_NFE=8.95528e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-103;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06147e-06;Hom=0;AF_POPMAX=8.95528e-06;AN_POPMAX=111666;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41411e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.13462e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=104;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.43219e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592782.1:c.1227C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,cDNA_position=1358,CDS_position=1227,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=409,Codons=aaC/aaT,MINIMISED=1,HGVSc=ENST00000592782.1:c.1227C>T
CDS|ENST00000592782	VCF	synonymous_variant	1367	1367	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-269;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41048e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=229;AF_Female=8.98037e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.09084e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.1236C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1367,CDS_position=1236,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs759148893,VARIANT_CLASS=SNV,Protein_position=412,Codons=acC/acT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1236C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1379	1379	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-97;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=60;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.19242e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.1248C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,cDNA_position=1379,CDS_position=1248,SYMBOL=NMT1,Existing_variation=rs773592883,VARIANT_CLASS=SNV,Protein_position=416,Codons=ctC/ctT,MINIMISED=1,HGVSc=ENST00000592782.1:c.1248C>T
CDS|ENST00000592782	VCF	synonymous_variant	1400	1400	0.0	.	.	AC_Male=0;AF_NFE=8.95111e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-104;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12117e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.61430e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=185;AF_Female=1.79598e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.43594e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.236e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=Y,HGVSp=ENST00000592782.1:c.1269C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1400,CDS_position=1269,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764809965,VARIANT_CLASS=SNV,Protein_position=423,Codons=taC/taT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1269C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1403	1403	0.0	.	.	AC_Male=4;AF_NFE=9.84640e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|3|6|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-207;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=13;Hom_NFE=0;AF=5.27880e-05;Hom=0;AF_POPMAX=9.84640e-05;AN_POPMAX=111716;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;AF_Male=2.96498e-05;AF_AFR=0.00000e+00;AC_raw=13;AB_MEDIAN=4.68254e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=147;AF_Female=8.08190e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|13;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=NFE;AC_POPMAX=11;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.27872e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:5.765e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0002,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001049,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592782.1:c.1272C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1403,CDS_position=1272,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs143838999,VARIANT_CLASS=SNV,Protein_position=424,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:5.765e-05,HGVSc=ENST00000592782.1:c.1272C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1439	1439	0.0	.	.	AC_Male=3;AF_NFE=2.68548e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-136;AF_OTH=3.64564e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03074e-05;Hom=0;AF_POPMAX=2.68548e-05;AN_POPMAX=111712;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|1;AF_Male=2.22397e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.47154e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=1.79659e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52266e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592782.1:c.1308C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1439,CDS_position=1308,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766390878,VARIANT_CLASS=SNV,Protein_position=436,Codons=agC/agT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1308C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1442	1442	0.0	.	.	AC_Male=7;AF_NFE=2.68567e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|3|1|1|4|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-92;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=10;Hom_NFE=0;AF=4.06187e-05;Hom=0;AF_POPMAX=1.94919e-04;AN_POPMAX=30782;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|1|0|1|0|0|1|1|1;AF_Male=5.18988e-05;AF_AFR=6.53424e-05;AC_raw=11;AB_MEDIAN=4.30556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=100;AF_Female=2.69508e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|10;Hom_raw=0;AF_SAS=1.94919e-04;AS_RF=9.08157e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=6;POPMAX=SAS;AC_POPMAX=6;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.942e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:2.997e-05,AFR_MAF=T:0.0002422,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000592782.1:c.1311C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1442,CDS_position=1311,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754018187,VARIANT_CLASS=SNV,Protein_position=437,Codons=gaC/gaT,MINIMISED=1,ExAC_AFR_MAF=T:4.942e-05,HGVSc=ENST00000592782.1:c.1311C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1454	1454	0.0	.	.	AC_Male=4;AF_NFE=1.79067e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-126;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62555e-05;Hom=0;AF_POPMAX=1.15955e-04;AN_POPMAX=17248;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AF_Male=2.96665e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.64516e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=66;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41995e-01;Hom_AMR=0;AC_EAS=2;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.15955e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.1323C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,cDNA_position=1454,CDS_position=1323,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=441,Codons=ctC/ctT,MINIMISED=1,HGVSc=ENST00000592782.1:c.1323C>T
CDS|ENST00000592782	VCF	synonymous_variant	1457	1457	0.0	.	.	AC_Male=4;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|4|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-155;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25216e-05;Hom=0;AF_POPMAX=4.63822e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|1|0|0|0;AF_Male=2.96754e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.85450e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=3.59719e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36108e-01;Hom_AMR=0;AC_EAS=8;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=4.63822e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=8;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592782.1:c.1326C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1457,CDS_position=1326,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778948819,VARIANT_CLASS=SNV,Protein_position=442,Codons=gcC/gcT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1326C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1493	1493	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98420e-125;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43637e-05;Hom=0;AF_POPMAX=1.78667e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3|1|1|0|1;AF_Male=2.22374e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.95800e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=2.69397e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43239e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=1.78667e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000592782.1:c.1362T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=C:0,cDNA_position=1493,CDS_position=1362,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs771722999,VARIANT_CLASS=SNV,Protein_position=454,Codons=gaT/gaC,MINIMISED=1,ExAC_AFR_MAF=C:1.647e-05,HGVSc=ENST00000592782.1:c.1362T>C,ExAC_Adj_MAF=C:0.0001729
CDS|ENST00000592782	VCF	synonymous_variant	1511	1511	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-79;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.23077e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=78;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.1380C>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=12/13,cDNA_position=1511,CDS_position=1380,SYMBOL=NMT1,Existing_variation=rs376284001,VARIANT_CLASS=SNV,Protein_position=460,Codons=acC/acA,MINIMISED=1,HGVSc=ENST00000592782.1:c.1380C>A
CDS|ENST00000592782	VCF	synonymous_variant	1514	1514	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-60;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12130e-06;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.41246e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.47362e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.50841e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,GMAF=T:0.0002,Amino_acids=F,HGVSp=ENST00000592782.1:c.1383C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=T:0,cDNA_position=1514,CDS_position=1383,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs556448466,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=461,AA_MAF=T:0.001,Codons=ttC/ttT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1383C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1517	1517	0.0	.	.	AC_Male=1;AF_NFE=1.79025e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-108;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12130e-06;Hom=0;AF_POPMAX=1.79025e-05;AN_POPMAX=111716;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.41246e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.68750e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=93;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.998e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.1386G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=A:0,cDNA_position=1517,CDS_position=1386,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs372878120,VARIANT_CLASS=SNV,Protein_position=462,Codons=ctG/ctA,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592782.1:c.1386G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	synonymous_variant	1526	1526	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-134;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53424e-05;AC_raw=1;AB_MEDIAN=5.44304e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41092e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592782.1:c.1395C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=G:9.61e-05,cDNA_position=1526,CDS_position=1395,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763355938,VARIANT_CLASS=SNV,Protein_position=465,Codons=ctC/ctG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.1395C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	synonymous_variant	1535	1535	0.0	.	.	AC_Male=3;AF_NFE=4.47555e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-85;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03034e-05;Hom=0;AF_POPMAX=4.47555e-05;AN_POPMAX=111718;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|1|1|1|0|0|1|0|0;AF_Male=2.22374e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.12195e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=66;AF_Female=1.79604e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20461e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592782.1:c.1404C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=T:0,cDNA_position=1535,CDS_position=1404,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs369290804,VARIANT_CLASS=SNV,Protein_position=468,Codons=ggC/ggT,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000592782.1:c.1404C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1544	1544	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-125;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.21277e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08869e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000592782.1:c.1413C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=12/13,cDNA_position=1544,CDS_position=1413,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=471,Codons=gaC/gaT,MINIMISED=1,HGVSc=ENST00000592782.1:c.1413C>T
CDS|ENST00000592782	VCF	synonymous_variant	1571	1571	0.0	.	.	AC_Male=6;AF_NFE=1.79029e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|0|5|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-97;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=9;Hom_NFE=0;AF=3.65470e-05;Hom=0;AF_POPMAX=7.10804e-04;AN_POPMAX=9848;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|3|0|3|0|0|0|1;AF_Male=4.44754e-05;AF_AFR=0.00000e+00;AC_raw=9;AB_MEDIAN=5.10204e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=7.10804e-04;DP_MEDIAN=77;AF_Female=2.69416e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|9;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08147e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=7;AF_raw=3.65450e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=C:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:4.497e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592782.1:c.1440T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,EA_MAF=C:0,Allele=C,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=C:0,cDNA_position=1571,CDS_position=1440,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs373214072,VARIANT_CLASS=SNV,Protein_position=480,Codons=aaT/aaC,MINIMISED=1,ExAC_AFR_MAF=C:2.471e-05,HGVSc=ENST00000592782.1:c.1440T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	synonymous_variant	1580	1580	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-54;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21834e-05;Hom=0;AF_POPMAX=9.74596e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=3.92157e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=51;AF_Female=2.69450e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=9.74596e-05;AS_RF=9.33552e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0001212,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=C,HGVSp=ENST00000592782.1:c.1449C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=T:0,cDNA_position=1580,CDS_position=1449,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs767877724,VARIANT_CLASS=SNV,Protein_position=483,Codons=tgC/tgT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.1449C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	synonymous_variant	1583	1583	0.0	.	.	AC_Male=23;AF_NFE=9.84798e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|2|8|16|9|8|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-97;AF_OTH=3.64697e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=45;Hom_NFE=0;AF=1.82747e-04;Hom=0;AF_POPMAX=2.64013e-03;AN_POPMAX=9848;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|0|1|5|1|3|2|9|4|3|4|1|3|4;AF_Male=1.70497e-04;AF_AFR=0.00000e+00;AC_raw=45;AB_MEDIAN=4.87500e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=2.64013e-03;DP_MEDIAN=69;AF_Female=1.97589e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|45;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99273e-01;Hom_AMR=0;AC_EAS=0;AC_Female=22;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=26;AC_AFR=0;Hom_SAS=0;AC_ASJ=26;AF_raw=1.82725e-04;Hom_Female=0;AF_AMR=1.78667e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:0.0001401,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.000225,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592782.1:c.1452C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=12/13,ExAC_AMR_MAF=T:0,cDNA_position=1583,CDS_position=1452,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs200139594&COSM3672473,VARIANT_CLASS=SNV,Protein_position=484,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:1.400e-04,HGVSc=ENST00000592782.1:c.1452C>T,ExAC_Adj_MAF=T:0.000173
CDS|ENST00000592782	VCF	synonymous_variant	1598	1598	0.0	.	.	AC_Male=1;AF_NFE=8.95608e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-115;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06220e-06;Hom=0;AF_POPMAX=8.95608e-06;AN_POPMAX=111656;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41455e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=90;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000592782.1:c.1467G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=12/13,cDNA_position=1598,CDS_position=1467,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=489,Codons=gaG/gaA,MINIMISED=1,HGVSc=ENST00000592782.1:c.1467G>A
CDS|ENST00000592782	VCF	synonymous_variant	1613	1613	0.0	.	.	AC_Male=6;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|3|0|1|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-82;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.85095e-05;Hom=0;AF_POPMAX=2.28624e-04;AN_POPMAX=30618;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|1|0|0|0|0|1|1|2|0|0;AF_Male=4.45778e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=9.01421e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=2.28624e-04;AS_RF=9.45417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=7;POPMAX=SAS;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84239e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000592782.1:c.1482G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=13/13,cDNA_position=1613,CDS_position=1482,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=494,Codons=gtG/gtA,MINIMISED=1,HGVSc=ENST00000592782.1:c.1482G>A
CDS|ENST00000592782	VCF	stop_gained	591	591	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=3.98107e-106;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=4.48511e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06412e-06;Hom=0;AF_POPMAX=4.48511e-05;AN_POPMAX=22296;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41983e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.88235e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=68;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.32793e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,LoF=HC,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,LoF_info=POSITION:0.308517773306506&ANN_ORF:521.9788&MAX_ORF:521.9788,Consequence=stop_gained,Amino_acids=Q/*,HGVSp=ENSP00000468424.1:p.Gln154Ter,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=HIGH,EXON=5/13,cDNA_position=591,CDS_position=460,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=154,Codons=Cag/Tag,MINIMISED=1,HGVSc=ENST00000592782.1:c.460C>T
CDS|ENST00000592782	VCF	stop_gained	1146	1146	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=5;AB_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.42754e-01;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=1.31183e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=0.00000e+00;GQ_HIST_ALT=1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.16590e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,LoF=HC,UNIPARC=UPI0000130275,PHENO=1,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,LoF_info=POSITION:0.68075117370892&ANN_ORF:626.8688&MAX_ORF:626.8688,Consequence=stop_gained,Amino_acids=R/*,HGVSp=ENSP00000468424.1:p.Arg339Ter,STRAND=1,CCDS=CCDS11494.1,SOMATIC=1,Allele=T,IMPACT=HIGH,EXON=10/13,cDNA_position=1146,CDS_position=1015,SYMBOL=NMT1,Existing_variation=COSM187889,VARIANT_CLASS=SNV,Protein_position=339,Codons=Cga/Tga,MINIMISED=1,HGVSc=ENST00000592782.1:c.1015C>T
CDS|ENST00000592782	VCF	frameshift_variant	1537	1538	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.00000e-62;AF_OTH=0.00000e+00;alleles=TA%2CT;AF_FIN=4.48430e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=4.48430e-05;AN_POPMAX=22300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.62267e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,LoF=HC,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,LoF_info=POSITION:0.943661971830986&ANN_ORF:396.74&MAX_ORF:396.74,Consequence=frameshift_variant,Amino_acids=I/X,HGVSp=ENSP00000468424.1:p.Ile469MetfsTer79,STRAND=1,CCDS=CCDS11494.1,Allele=-,IMPACT=HIGH,EXON=12/13,cDNA_position=1538,CDS_position=1407,SYMBOL=NMT1,VARIANT_CLASS=deletion,Protein_position=469,Codons=atA/at,MINIMISED=1,HGVSc=ENST00000592782.1:c.1407delA
CDS|ENST00000592782	VCF	missense_variant	136	136	0.0	.	.	AC_Male=0;AF_NFE=9.04748e-06;Hom_FIN=0;GQ_MEDIAN=20;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.90099e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.19363e-06;Hom=0;AF_POPMAX=3.00571e-05;AN_POPMAX=33270;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.81594e-05;GQ_HIST_ALT=0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.32038e-03;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=3.00571e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.651e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000468424.1:p.Ala2Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=136,CDS_position=5,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs771527303,VARIANT_CLASS=SNV,Protein_position=2,Codons=gCg/gTg,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000592782.1:c.5C>T,ExAC_Adj_MAF=T:8.965e-05
CDS|ENST00000592782	VCF	missense_variant	138	138	0.0	.	.	AC_Male=1;AF_NFE=9.02755e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-30;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.17307e-06;Hom=0;AF_POPMAX=6.58762e-05;AN_POPMAX=15180;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44923e-06;AF_AFR=6.58762e-05;AC_raw=2;AB_MEDIAN=4.35484e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=9.05272e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20566e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.622e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.564e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.823),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=D/H,HGVSp=ENSP00000468424.1:p.Asp3His,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=C:0,cDNA_position=138,CDS_position=7,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs772761859,VARIANT_CLASS=SNV,Protein_position=3,Codons=Gac/Cac,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000592782.1:c.7G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	141	141	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16887e-06;Hom=0;AF_POPMAX=6.51339e-05;AN_POPMAX=30706;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=1.80973e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.51339e-05;AS_RF=9.34226e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.069),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000468424.1:p.Glu4Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,cDNA_position=141,CDS_position=10,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=4,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000592782.1:c.10G>A
CDS|ENST00000592782	VCF	missense_variant	142	142	0.0	.	.	AC_Male=0;AF_NFE=9.01990e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08360e-06;Hom=0;AF_POPMAX=9.01990e-06;AN_POPMAX=110866;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=9.04732e-06;GQ_HIST_ALT=0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17447e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.595e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.559e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.066),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/G,HGVSp=ENSP00000468424.1:p.Glu4Gly,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=142,CDS_position=11,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs760309598,VARIANT_CLASS=SNV,Protein_position=4,Codons=gAg/gGg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.11A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	144	144	0.0	.	.	AC_Male=31;AF_NFE=9.01518e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|4|2|10|15|9|8|6|1|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.15479e-38;AF_OTH=3.66838e-04;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=56;Hom_NFE=0;AF=2.28573e-04;Hom=0;AF_POPMAX=3.07603e-03;AN_POPMAX=17230;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|3|15|10|7|8|3|3|1|4|1|1|0|0|0|0|0|0;AF_Male=2.30614e-04;AF_AFR=0.00000e+00;AC_raw=56;AB_MEDIAN=4.76557e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=2.26093e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|56;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.34281e-01;Hom_AMR=0;AC_EAS=53;AC_Female=25;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.07603e-03;AC_SAS=0;POPMAX=EAS;AC_POPMAX=53;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.27391e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.08),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:0.0002232,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,EAS_MAF=C:0,EUR_MAF=C:0.001,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0.002947,ENSP=ENSP00000468424,Consequence=missense_variant,GMAF=C:0.0002,Amino_acids=S/R,HGVSp=ENSP00000468424.1:p.Ser5Arg,STRAND=1,ExAC_SAS_MAF=C:0.001171,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=C:0,cDNA_position=144,CDS_position=13,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs564172691,SAS_MAF=C:0,VARIANT_CLASS=SNV,Protein_position=5,AA_MAF=C:0,Codons=Agt/Cgt,MINIMISED=1,ExAC_AFR_MAF=C:2.142e-04,HGVSc=ENST00000592782.1:c.13A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	145	145	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08090e-06;Hom=0;AF_POPMAX=3.25330e-05;AN_POPMAX=30738;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43760e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25330e-05;AS_RF=8.76833e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.39),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=S/N,HGVSp=ENSP00000468424.1:p.Ser5Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,cDNA_position=145,CDS_position=14,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=5,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000592782.1:c.14G>A
CDS|ENST00000592782	VCF	missense_variant	150	150	0.0	.	.	AC_Male=0;AF_NFE=9.01372e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-34;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08110e-06;Hom=0;AF_POPMAX=9.01372e-06;AN_POPMAX=110942;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.80000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.04454e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06165e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.623),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/P,HGVSp=ENSP00000468424.1:p.Thr7Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,cDNA_position=150,CDS_position=19,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=7,Codons=Aca/Cca,MINIMISED=1,HGVSc=ENST00000592782.1:c.19A>C
CDS|ENST00000592782	VCF	missense_variant	153	153	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52365e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.887),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000468424.1:p.Ala8Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,cDNA_position=153,CDS_position=22,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=Gca/Aca,HGVSc=ENST00000592782.1:c.22G>A
CDS|ENST00000592782	VCF	missense_variant	153	153	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-45;AF_OTH=1.83756e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08320e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.05108e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.37319e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.976),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/P,HGVSp=ENSP00000468424.1:p.Ala8Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,cDNA_position=153,CDS_position=22,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=Gca/Cca,HGVSc=ENST00000592782.1:c.22G>C
CDS|ENST00000592782	VCF	missense_variant	154	154	0.0	.	.	AC_Male=4;AF_NFE=9.02104e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-43;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63397e-05;Hom=0;AF_POPMAX=9.75864e-05;AN_POPMAX=30742;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=2.97699e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.70769e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=9.75864e-05;AS_RF=9.42769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.713e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.554e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.2),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000468424.1:p.Ala8Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=154,CDS_position=23,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764406772,VARIANT_CLASS=SNV,Protein_position=8,Codons=gCa/gTa,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.23C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	156	156	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-39;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08257e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=9.04846e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.15769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.28),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.556e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000468424.1:p.Val9Leu,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=C:0,cDNA_position=156,CDS_position=25,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs752105945,VARIANT_CLASS=SNV,Protein_position=9,Codons=Gtg/Ctg,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000592782.1:c.25G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	162	162	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.87339e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.63),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.554e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000468424.1:p.Pro11Ser,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=162,CDS_position=31,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=11,Codons=Ccg/Tcg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592782.1:c.31C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	162	162	0.0	.	.	AC_Male=0;AF_NFE=9.02006e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38634e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08397e-06;Hom=0;AF_POPMAX=9.02006e-06;AN_POPMAX=110864;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.70833e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=18;AF_Female=9.05403e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.26525e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.49),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.554e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.007),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/T,HGVSp=ENSP00000468424.1:p.Pro11Thr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=162,CDS_position=31,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=11,Codons=Ccg/Acg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592782.1:c.31C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	163	163	0.0	.	.	AC_Male=2;AF_NFE=9.01664e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-48;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16573e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48792e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63469e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.40560e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.3),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.552e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000468424.1:p.Pro11Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=163,CDS_position=32,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs750513385,VARIANT_CLASS=SNV,Protein_position=11,Codons=cCg/cTg,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.32C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	166	166	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=62;AB_HIST_ALT=0|0|2|0|0|2|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25280e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22474e-05;Hom=0;AF_POPMAX=6.50703e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|1|0|2|0|1|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44025e-06;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=1.80920e-05;GQ_HIST_ALT=1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.50703e-05;AS_RF=1.16160e-02;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=2.98401e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000468424.1:p.Pro12Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=166,CDS_position=35,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=12,Codons=cCg/cTg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.35C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	166	166	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=58;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.80083e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08247e-06;Hom=0;AF_POPMAX=3.25351e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.95563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=9.04601e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25351e-05;AS_RF=1.45870e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.3),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.093),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/Q,HGVSp=ENSP00000468424.1:p.Pro12Gln,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=166,CDS_position=35,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=12,Codons=cCg/cAg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.35C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	168	168	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-63;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08007e-06;Hom=0;AF_POPMAX=5.80181e-05;AN_POPMAX=17236;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60976e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96821e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.09),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.053),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/P,HGVSp=ENSP00000468424.1:p.Ala13Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,cDNA_position=168,CDS_position=37,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=13,Codons=Gca/Cca,MINIMISED=1,HGVSc=ENST00000592782.1:c.37G>C
CDS|ENST00000592782	VCF	missense_variant	171	171	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97164e-32;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15627e-06;Hom=0;AF_POPMAX=1.16063e-04;AN_POPMAX=17232;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.57018e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80682e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52227e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.16063e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.49),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.534e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.035),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0.0001174,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000468424.1:p.Pro14Ser,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=171,CDS_position=40,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754859910,VARIANT_CLASS=SNV,Protein_position=14,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000592782.1:c.40C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	172	172	0.0	.	.	AC_Male=1;AF_NFE=2.69964e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.37387e-64;AF_OTH=1.83217e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63090e-05;Hom=0;AF_POPMAX=2.69964e-05;AN_POPMAX=111126;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.03446e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=2.70929e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36654e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.33),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000468424.1:p.Pro14Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/13,cDNA_position=172,CDS_position=41,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=14,Codons=cCt/cTt,MINIMISED=1,HGVSc=ENST00000592782.1:c.41C>T
CDS|ENST00000592782	VCF	missense_variant	175	175	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-53;AF_OTH=1.83083e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22264e-05;Hom=0;AF_POPMAX=6.58068e-05;AN_POPMAX=15196;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43262e-06;AF_AFR=6.58068e-05;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=1.80460e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35197e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=T:0.0014,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=missense_variant,GMAF=T:0.0002,ExAC_SAS_MAF=T:0,IMPACT=MODERATE,ExAC_AMR_MAF=T:0.0001013,CDS_position=44,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs202061902,VARIANT_CLASS=SNV,Protein_position=15,AA_MAF=T:0,Codons=cCg/cTg,ExAC_Adj_MAF=T:8.969e-05,ExAC_EAS_MAF=T:1.705e-05,ExAC_MAF=T:0,BIOTYPE=protein_coding,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.008),ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Amino_acids=P/L,HGVSp=ENSP00000468424.1:p.Pro15Leu,STRAND=1,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=T,EXON=2/13,cDNA_position=175,SAS_MAF=T:0,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.44C>T
CDS|ENST00000592782	VCF	missense_variant	178	178	0.0	.	.	AC_Male=1;AF_NFE=8.98893e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-25;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07236e-06;Hom=0;AF_POPMAX=8.98893e-06;AN_POPMAX=111248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42765e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.62500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.15),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.703e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.089e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/R,HGVSp=ENSP00000468424.1:p.Leu16Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=178,CDS_position=47,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772038652,VARIANT_CLASS=SNV,Protein_position=16,Codons=cTg/cGg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.47T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	187	187	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-33;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14120e-06;Hom=0;AF_POPMAX=5.96019e-05;AN_POPMAX=33556;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42589e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.78231e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=5.96019e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.94),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000468424.1:p.Met19Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,cDNA_position=187,CDS_position=56,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=19,Codons=aTg/aGg,HGVSc=ENST00000592782.1:c.56T>G
CDS|ENST00000592782	VCF	missense_variant	187	187	0.0	.	.	AC_Male=0;AF_NFE=8.98650e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-65;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07060e-06;Hom=0;AF_POPMAX=8.98650e-06;AN_POPMAX=111278;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43341e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.17),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.01),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/T,HGVSp=ENSP00000468424.1:p.Met19Thr,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,cDNA_position=187,CDS_position=56,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=19,Codons=aTg/aCg,HGVSc=ENST00000592782.1:c.56T>C
CDS|ENST00000592782	VCF	missense_variant	190	190	0.0	.	.	AC_Male=7;AF_NFE=9.88373e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|3|1|3|3|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-45;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.47784e-05;Hom=0;AF_POPMAX=9.88373e-05;AN_POPMAX=111294;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|4|0|1|0|2|0|1|0|1|0|0|0|0;AF_Male=5.19889e-05;AF_AFR=0.00000e+00;AC_raw=11;AB_MEDIAN=4.18860e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.60328e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=11;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.14),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:7.653e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0.0001388,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.012),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000468424.1:p.Met20Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=190,CDS_position=59,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772952636,VARIANT_CLASS=SNV,Protein_position=20,Codons=aTg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:7.413e-05,HGVSc=ENST00000592782.1:c.59T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	201	201	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=52;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.20127e-01;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07090e-06;Hom=0;AF_POPMAX=2.98098e-05;AN_POPMAX=33546;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.16667e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.00836e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.23972e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=2.98098e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.52e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.07),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/R,HGVSp=ENSP00000468424.1:p.Gly24Arg,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=201,CDS_position=70,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746539074,VARIANT_CLASS=SNV,Protein_position=24,Codons=Ggg/Agg,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592782.1:c.70G>A,ExAC_Adj_MAF=A:9.027e-05
CDS|ENST00000592782	VCF	missense_variant	202	202	0.0	.	.	AC_Male=1;AF_NFE=8.98182e-06;Hom_FIN=0;GQ_MEDIAN=54;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.54545e-02;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98182e-06;AN_POPMAX=111336;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42688e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.26923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.37827e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.47),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/A,HGVSp=ENSP00000468424.1:p.Gly24Ala,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,cDNA_position=202,CDS_position=71,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=24,Codons=gGg/gCg,MINIMISED=1,HGVSc=ENST00000592782.1:c.71G>C
CDS|ENST00000592782	VCF	missense_variant	207	207	0.0	.	.	AC_Male=0;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.53267e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07070e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.38095e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.00722e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.31156e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.529e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.546e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000468424.1:p.Gly26Ser,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=207,CDS_position=76,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs770300796,VARIANT_CLASS=SNV,Protein_position=26,Codons=Ggc/Agc,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592782.1:c.76G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	212	212	0.0	.	.	AC_Male=1;AF_NFE=8.98101e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98101e-06;AN_POPMAX=111346;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42721e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.37664e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.73),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.539e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.547e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.493),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=H/Q,HGVSp=ENSP00000468424.1:p.His27Gln,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=212,CDS_position=81,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs776300314,VARIANT_CLASS=SNV,Protein_position=27,Codons=caT/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.81T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	214	214	0.0	.	.	AC_Male=0;AF_NFE=8.98505e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.31688e-02;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07130e-06;Hom=0;AF_POPMAX=8.98505e-06;AN_POPMAX=111296;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.51984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.00690e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.21757e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,PHENO=1,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/V,HGVSp=ENSP00000468424.1:p.Glu28Val,STRAND=1,CCDS=CCDS11494.1,SOMATIC=1,Allele=T,IMPACT=MODERATE,EXON=2/13,cDNA_position=214,CDS_position=83,SYMBOL=NMT1,Existing_variation=COSM1128678,VARIANT_CLASS=SNV,Protein_position=28,Codons=gAg/gTg,MINIMISED=1,HGVSc=ENST00000592782.1:c.83A>T
CDS|ENST00000592782	VCF	missense_variant	218	218	0.0	.	.	AC_Male=0;AF_NFE=8.98957e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-73;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07286e-06;Hom=0;AF_POPMAX=8.98957e-06;AN_POPMAX=111240;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.37037e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=9.01128e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05502e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.13),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.571e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.553e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.397),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=H/Q,HGVSp=ENSP00000468424.1:p.His29Gln,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=218,CDS_position=87,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759161485,VARIANT_CLASS=SNV,Protein_position=29,Codons=caC/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.87C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	220	220	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-32;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07425e-06;Hom=0;AF_POPMAX=5.80518e-05;AN_POPMAX=17226;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43362e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.34667e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80518e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.588e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.781),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0.0001181,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=C/Y,HGVSp=ENSP00000468424.1:p.Cys30Tyr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=220,CDS_position=89,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764495116,VARIANT_CLASS=SNV,Protein_position=30,Codons=tGc/tAc,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592782.1:c.89G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	222	222	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-26;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22221e-05;Hom=0;AF_POPMAX=8.96111e-05;AN_POPMAX=33478;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43329e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.21053e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.80297e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.53191e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=8.96111e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.55),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.721e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.248),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=S/G,HGVSp=ENSP00000468424.1:p.Ser31Gly,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=222,CDS_position=91,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774684452,VARIANT_CLASS=SNV,Protein_position=31,Codons=Agc/Ggc,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.91A>G,ExAC_Adj_MAF=G:0.0001836
CDS|ENST00000592782	VCF	missense_variant	251	251	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-29;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=3.26861e-05;AN_POPMAX=30594;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.47005e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.26861e-05;AS_RF=8.82577e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.21),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.018e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=S/R,HGVSp=ENSP00000468424.1:p.Ser40Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=251,CDS_position=120,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=40,Codons=agC/agG,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.120C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	253	253	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92478e-20;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09799e-06;Hom=0;AF_POPMAX=5.83158e-05;AN_POPMAX=17148;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.91667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07293e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.95804e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.83158e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.058e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.293),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0.0001227,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=Y/C,HGVSp=ENSP00000468424.1:p.Tyr41Cys,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=253,CDS_position=122,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756247053,VARIANT_CLASS=SNV,Protein_position=41,Codons=tAc/tGc,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.122A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	256	256	0.0	.	.	AC_Male=1;AF_NFE=9.07738e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-55;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.11265e-06;Hom=0;AF_POPMAX=9.07738e-06;AN_POPMAX=110164;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49805e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.29412e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.17479e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06068e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.93),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000468424.1:p.Asn42Ser,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/13,cDNA_position=256,CDS_position=125,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=42,Codons=aAc/aGc,MINIMISED=1,HGVSc=ENST00000592782.1:c.125A>G
CDS|ENST00000592782	VCF	missense_variant	259	259	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=7;AB_HIST_ALT=0|0|2|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.66338e-01;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=4.53227e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12712e-06;Hom=0;AF_POPMAX=4.53227e-05;AN_POPMAX=22064;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.52298e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.73728e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21819e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.125),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/P,HGVSp=ENSP00000468424.1:p.Arg43Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/13,cDNA_position=259,CDS_position=128,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=43,Codons=cGg/cCg,MINIMISED=1,HGVSc=ENST00000592782.1:c.128G>C
CDS|ENST00000592782	VCF	missense_variant	267	267	0.0	.	.	AC_Male=1;AF_NFE=9.20793e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-78;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13846e-06;Hom=0;AF_POPMAX=9.20793e-06;AN_POPMAX=108602;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.53477e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=50;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.26429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09934e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.76),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.304e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.508e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.037),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000468424.1:p.Leu46Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/13,ExAC_AMR_MAF=G:0,cDNA_position=267,CDS_position=136,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs758247752,VARIANT_CLASS=SNV,Protein_position=46,Codons=Ttg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.136T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	268	268	0.0	.	.	AC_Male=1;AF_NFE=9.20082e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-91;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13363e-06;Hom=0;AF_POPMAX=9.20082e-06;AN_POPMAX=108686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.52627e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.83900e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.05),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.624),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/W,HGVSp=ENSP00000468424.1:p.Leu46Trp,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/13,cDNA_position=268,CDS_position=137,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=46,Codons=tTg/tGg,MINIMISED=1,HGVSc=ENST00000592782.1:c.137T>G
CDS|ENST00000592782	VCF	missense_variant	271	271	0.0	.	.	AC_Male=1;AF_NFE=9.18628e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-41;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12361e-06;Hom=0;AF_POPMAX=9.18628e-06;AN_POPMAX=108858;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.50875e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.88840e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09927e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.073),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=S/N,HGVSp=ENSP00000468424.1:p.Ser47Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=3/13,cDNA_position=271,CDS_position=140,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=47,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000592782.1:c.140G>A
CDS|ENST00000592782	VCF	missense_variant	273	273	0.0	.	.	AC_Male=0;AF_NFE=9.18577e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-80;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12368e-06;Hom=0;AF_POPMAX=9.18577e-06;AN_POPMAX=108864;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=9.14645e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40367e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.2),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000468424.1:p.Pro48Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/13,cDNA_position=273,CDS_position=142,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=48,Codons=Cca/Gca,MINIMISED=1,HGVSc=ENST00000592782.1:c.142C>G
CDS|ENST00000592782	VCF	missense_variant	279	279	0.0	.	.	AC_Male=6;AF_NFE=4.58573e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|3|2|4|8|1|1|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-54;AF_OTH=1.83352e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=21;Hom_NFE=0;AF=8.63501e-05;Hom=0;AF_POPMAX=9.81804e-04;AN_POPMAX=15278;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|2|5|2|2|2|0|3|0|0|1|0|1|0|0|1;AF_Male=4.49384e-05;AF_AFR=9.81804e-04;AC_raw=21;AB_MEDIAN=5.21739e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=1.36761e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|21;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=15;AC_AFR=15;Hom_SAS=0;AC_ASJ=0;AF_raw=8.60860e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.71),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=G:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=G:0,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=missense_variant,GMAF=G:0.0002,ExAC_SAS_MAF=G:0,IMPACT=MODERATE,ExAC_AMR_MAF=G:0.000789,CDS_position=148,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs140455291,VARIANT_CLASS=SNV,Protein_position=50,AA_MAF=G:0,Codons=Aat/Gat,ExAC_Adj_MAF=G:0,ExAC_EAS_MAF=G:8.336e-05,ExAC_MAF=G:0,BIOTYPE=protein_coding,ExAC_OTH_MAF=G:3.034e-05,AFR_MAF=G:0,SWISSPROT=P30419,EUR_MAF=G:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Amino_acids=N/D,HGVSp=ENSP00000468424.1:p.Asn50Asp,STRAND=1,CCDS=CCDS11494.1,EA_MAF=G:0.0011,Allele=G,EXON=3/13,cDNA_position=279,SAS_MAF=G:0,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-05,HGVSc=ENST00000592782.1:c.148A>G
CDS|ENST00000592782	VCF	missense_variant	280	280	0.0	.	.	AC_Male=2;AF_NFE=5.50327e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.29463e-76;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.46765e-05;Hom=0;AF_POPMAX=5.50327e-05;AN_POPMAX=109026;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AF_Male=1.49817e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.64551e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=3.64797e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53507e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.45964e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.45),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:2.508e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:4.569e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.017),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000468424.1:p.Asn50Ser,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/13,ExAC_AMR_MAF=G:0,cDNA_position=280,CDS_position=149,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs757177482,VARIANT_CLASS=SNV,Protein_position=50,Codons=aAt/aGt,MINIMISED=1,ExAC_AFR_MAF=G:2.471e-05,HGVSc=ENST00000592782.1:c.149A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	292	292	0.0	.	.	AC_Male=3;AF_NFE=4.59441e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|2|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-54;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.05744e-05;Hom=0;AF_POPMAX=4.59441e-05;AN_POPMAX=108828;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|2|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24908e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.80645e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.82428e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99531e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.04965e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.11),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.372e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.027e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000468424.1:p.Ala54Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=3/13,ExAC_AMR_MAF=T:0,cDNA_position=292,CDS_position=161,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs780748535,VARIANT_CLASS=SNV,Protein_position=54,Codons=gCc/gTc,MINIMISED=1,ExAC_AFR_MAF=T:4.118e-05,HGVSc=ENST00000592782.1:c.161C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	295	295	0.0	.	.	AC_Male=6;AF_NFE=6.46365e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|1|0|3|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-50;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.88843e-05;Hom=0;AF_POPMAX=6.46365e-05;AN_POPMAX=108298;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|2|1|1|0|0|0|0|0|1|0|0|0|0;AF_Male=4.50857e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.32432e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=9.15198e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.86984e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=possibly_damaging(0.72),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=K/R,HGVSp=ENSP00000468424.1:p.Lys55Arg,STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/13,ExAC_AMR_MAF=T:0&G:0,cDNA_position=295,CDS_position=164,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=55,Codons=aAa/aGa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000592782.1:c.164A>G,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000592782	VCF	missense_variant	295	295	0.0	.	.	AC_Male=1;AF_NFE=9.23378e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-64;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12633e-06;Hom=0;AF_POPMAX=9.23378e-06;AN_POPMAX=108298;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.51428e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.22727e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09977e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.033),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=K/I,HGVSp=ENSP00000468424.1:p.Lys55Ile,STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=3/13,ExAC_AMR_MAF=T:0&G:0,cDNA_position=295,CDS_position=164,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=55,Codons=aAa/aTa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000592782.1:c.164A>T,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000592782	VCF	missense_variant	307	307	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-24;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15155e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.12500e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=9.21302e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=2.89217e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10004e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.08),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=K/R,HGVSp=ENSP00000468424.1:p.Lys59Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/13,cDNA_position=307,CDS_position=176,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=59,Codons=aAg/aGg,MINIMISED=1,HGVSc=ENST00000592782.1:c.176A>G
CDS|ENST00000592782	VCF	missense_variant	324	324	0.0	.	.	AC_Male=0;AF_NFE=9.88807e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-130;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.33099e-06;Hom=0;AF_POPMAX=9.88807e-06;AN_POPMAX=101132;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.14563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=9.61908e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33183e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10129e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.315e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.529e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.013),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=K/E,HGVSp=ENSP00000468424.1:p.Lys65Glu,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/13,ExAC_AMR_MAF=G:0,cDNA_position=324,CDS_position=193,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779784731,VARIANT_CLASS=SNV,Protein_position=65,Codons=Aaa/Gaa,MINIMISED=1,ExAC_AFR_MAF=G:8.261e-06,HGVSc=ENST00000592782.1:c.193A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	334	334	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30719e-25;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.87099e-05;Hom=0;AF_POPMAX=1.31596e-04;AN_POPMAX=30396;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.55437e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.49730e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.03795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66438e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64119e-05;Hom_Female=0;AF_AMR=1.31596e-04;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.043),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/V,HGVSp=ENSP00000468424.1:p.Gly68Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=3/13,cDNA_position=334,CDS_position=203,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=68,Codons=gGc/gTc,MINIMISED=1,HGVSc=ENST00000592782.1:c.203G>T
CDS|ENST00000592782	VCF	missense_variant	351	351	0.0	.	.	AC_Male=1;AF_NFE=2.58685e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-31;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.06140e-05;Hom=0;AF_POPMAX=2.58685e-05;AN_POPMAX=77314;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=9.69330e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.87363e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.17280e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.91480e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.21760e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.19),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.017),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/S,HGVSp=ENSP00000468424.1:p.Ala74Ser,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=3/13,cDNA_position=351,CDS_position=220,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=74,Codons=Gcc/Tcc,MINIMISED=1,HGVSc=ENST00000592782.1:c.220G>T
CDS|ENST00000592782	VCF	missense_variant	352	352	0.0	.	.	AC_Male=0;AF_NFE=1.30774e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.34920e-06;Hom=0;AF_POPMAX=1.30774e-05;AN_POPMAX=76468;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.84615e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=65;AF_Female=1.18189e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.26907e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10985e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.15),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000468424.1:p.Ala74Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=3/13,cDNA_position=352,CDS_position=221,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=74,Codons=gCc/gTc,MINIMISED=1,HGVSc=ENST00000592782.1:c.221C>T
CDS|ENST00000592782	VCF	missense_variant	356	356	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-72;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.55759e-06;Hom=0;AF_POPMAX=3.91972e-05;AN_POPMAX=25512;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.22730e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.91972e-05;AS_RF=8.51470e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11306e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.12),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.163),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=Q/H,HGVSp=ENSP00000468424.1:p.Gln75His,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=3/13,cDNA_position=356,CDS_position=225,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=75,Codons=caG/caC,MINIMISED=1,HGVSc=ENST00000592782.1:c.225G>C
CDS|ENST00000592782	VCF	missense_variant	360	360	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=70;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97133e-05;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.12740e-05;Hom=0;AF_POPMAX=8.46453e-05;AN_POPMAX=11814;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.03086e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.94118e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=1.24387e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.04301e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=8.46453e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.23113e-06;Hom_Female=0;AF_AMR=3.93236e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.43),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.006),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=Q/K,HGVSp=ENSP00000468424.1:p.Gln77Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=3/13,cDNA_position=360,CDS_position=229,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=77,Codons=Cag/Aag,MINIMISED=1,HGVSc=ENST00000592782.1:c.229C>A
CDS|ENST00000592782	VCF	missense_variant	366	366	0.0	.	.	AC_Male=1;AF_NFE=2.98686e-05;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|2|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.19832e-05;Hom=0;AF_POPMAX=2.98686e-05;AN_POPMAX=66960;AC_NFE=2;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.09965e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.15047e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.31645e-05;GQ_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.22455e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64978e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.11),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.776e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:5.974e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.007),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/M,HGVSp=ENSP00000468424.1:p.Val79Met,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=3/13,ExAC_AMR_MAF=A:0,cDNA_position=366,CDS_position=235,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761306458,VARIANT_CLASS=SNV,Protein_position=79,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.569e-06,HGVSc=ENST00000592782.1:c.235G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	372	372	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-33;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.41163e-06;Hom=0;AF_POPMAX=6.76636e-05;AN_POPMAX=29558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.53130e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.32389e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.76636e-05;AS_RF=8.96351e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12123e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.81),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.681e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.000128,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=M/V,HGVSp=ENSP00000468424.1:p.Met81Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=G:0,cDNA_position=372,CDS_position=241,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767459577,VARIANT_CLASS=SNV,Protein_position=81,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.241A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	376	376	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51591e-22;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.09459e-05;AN_POPMAX=16408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.23913e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20091e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.09459e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.48),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.391e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=N/T,HGVSp=ENSP00000468424.1:p.Asn82Thr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=C,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=376,CDS_position=245,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=82,Codons=aAc/aCc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.245A>C,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	376	376	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-62;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.67646e-05;AN_POPMAX=14978;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.67646e-05;AC_raw=1;AB_MEDIAN=3.09859e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.02337e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.18),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.391e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=N/I,HGVSp=ENSP00000468424.1:p.Asn82Ile,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=376,CDS_position=245,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=82,Codons=aAc/aTc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.245A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	398	398	0.0	.	.	AC_Male=1;AF_NFE=9.04977e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-52;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10988e-06;Hom=0;AF_POPMAX=9.04977e-06;AN_POPMAX=110500;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49524e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.10256e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.90362e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.13),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.312e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.51e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=I/M,HGVSp=ENSP00000468424.1:p.Ile89Met,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=G:0,cDNA_position=398,CDS_position=267,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779405921,VARIANT_CLASS=SNV,Protein_position=89,Codons=atC/atG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.267C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	417	417	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-21;AF_OTH=1.83554e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08013e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.70588e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=9.03130e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.67445e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.29),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000468424.1:p.Ile96Val,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=4/13,cDNA_position=417,CDS_position=286,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=96,Codons=Att/Gtt,MINIMISED=1,HGVSc=ENST00000592782.1:c.286A>G
CDS|ENST00000592782	VCF	missense_variant	433	433	0.0	.	.	AC_Male=0;AF_NFE=8.97263e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-62;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07163e-06;Hom=0;AF_POPMAX=8.97263e-06;AN_POPMAX=111450;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=48;AF_Female=9.00739e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.18),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.258e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.129),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/E,HGVSp=ENSP00000468424.1:p.Val101Glu,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=A:0,cDNA_position=433,CDS_position=302,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs778561485,VARIANT_CLASS=SNV,Protein_position=101,Codons=gTg/gAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.302T>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	435	435	0.0	.	.	AC_Male=0;AF_NFE=8.97167e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-66;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07073e-06;Hom=0;AF_POPMAX=8.97167e-06;AN_POPMAX=111462;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.45455e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00414e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97942e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.41),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.258e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/C,HGVSp=ENSP00000468424.1:p.Gly102Cys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=T:0,cDNA_position=435,CDS_position=304,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs747390700,VARIANT_CLASS=SNV,Protein_position=102,Codons=Ggt/Tgt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.304G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	440	440	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-48;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07186e-06;Hom=0;AF_POPMAX=3.25563e-05;AN_POPMAX=30716;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43097e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25563e-05;AS_RF=9.07079e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.256e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.015),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=Q/H,HGVSp=ENSP00000468424.1:p.Gln103His,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=C:0,cDNA_position=440,CDS_position=309,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs771371139,VARIANT_CLASS=SNV,Protein_position=103,Codons=caG/caC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.309G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	441	441	0.0	.	.	AC_Male=1;AF_NFE=8.97392e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07279e-06;Hom=0;AF_POPMAX=8.97392e-06;AN_POPMAX=111434;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43152e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.97872e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.42544e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=A:0,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=missense_variant,GMAF=A:0.0002,ExAC_SAS_MAF=A:0,SOMATIC=0&1,IMPACT=MODERATE,ExAC_AMR_MAF=A:0,CDS_position=310,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs563736659&COSM1493963,VARIANT_CLASS=SNV,Protein_position=104,AA_MAF=A:0,Codons=Gga/Aga,ExAC_Adj_MAF=A:0,PHENO=0&1,ExAC_EAS_MAF=A:8.254e-06,BIOTYPE=protein_coding,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,SWISSPROT=P30419,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.067),ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Amino_acids=G/R,HGVSp=ENSP00000468424.1:p.Gly104Arg,STRAND=1,CCDS=CCDS11494.1,Allele=A,EXON=4/13,cDNA_position=441,SAS_MAF=A:0.001,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.310G>A
CDS|ENST00000592782	VCF	missense_variant	457	457	0.0	.	.	AC_Male=1;AF_NFE=8.98053e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-63;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07515e-06;Hom=0;AF_POPMAX=8.98053e-06;AN_POPMAX=111352;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43528e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.03846e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=52;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18859e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.35),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.249e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.501e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/T,HGVSp=ENSP00000468424.1:p.Met109Thr,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=C:0,cDNA_position=457,CDS_position=326,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs770043528,VARIANT_CLASS=SNV,Protein_position=109,Codons=aTg/aCg,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.326T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	468	468	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=7.94328e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=4.48632e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07581e-06;Hom=0;AF_POPMAX=4.48632e-05;AN_POPMAX=22290;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43572e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.25000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.10681e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.31),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=S/G,HGVSp=ENSP00000468424.1:p.Ser113Gly,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=4/13,cDNA_position=468,CDS_position=337,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=113,Codons=Agc/Ggc,MINIMISED=1,HGVSc=ENST00000592782.1:c.337A>G
CDS|ENST00000592782	VCF	missense_variant	475	475	0.0	.	.	AC_Male=1;AF_NFE=1.79727e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-36;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15328e-06;Hom=0;AF_POPMAX=1.79727e-05;AN_POPMAX=111280;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=9.02120e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.61453e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.259e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.155),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/L,HGVSp=ENSP00000468424.1:p.Arg115Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=T:0,cDNA_position=475,CDS_position=344,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs377156745&COSM436718,VARIANT_CLASS=SNV,Protein_position=115,Codons=cGa/cTa,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.344G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	477	477	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07525e-06;Hom=0;AF_POPMAX=3.25839e-05;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43550e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25839e-05;AS_RF=7.10677e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.66),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=S/R,HGVSp=ENSP00000468424.1:p.Ser116Arg,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=4/13,cDNA_position=477,CDS_position=346,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=116,Codons=Agc/Cgc,MINIMISED=1,HGVSc=ENST00000592782.1:c.346A>C
CDS|ENST00000592782	VCF	missense_variant	496	496	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.91433e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.37719e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.02383e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.859),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/M,HGVSp=ENSP00000468424.1:p.Thr122Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=T:0,cDNA_position=496,CDS_position=365,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=122,Codons=aCg/aTg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.365C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	496	496	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-14;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.51858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.945),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/R,HGVSp=ENSP00000468424.1:p.Thr122Arg,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=G,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=T:0,cDNA_position=496,CDS_position=365,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=122,Codons=aCg/aGg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.365C>G,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	504	504	0.0	.	.	AC_Male=0;AF_NFE=9.10167e-06;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|2|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13213e-06;Hom=0;AF_POPMAX=9.10167e-06;AN_POPMAX=109870;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=9.15131e-06;GQ_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.57813e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.387e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.253),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/I,HGVSp=ENSP00000468424.1:p.Val125Ile,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=A:0,cDNA_position=504,CDS_position=373,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761622308,VARIANT_CLASS=SNV,Protein_position=125,Codons=Gtc/Atc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.373G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	511	511	0.0	.	.	AC_Male=5;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|5|2|2|3|0|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-65;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.79897e-05;Hom=0;AF_POPMAX=9.23483e-04;AN_POPMAX=15160;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|3|1|1|1|0|0|0|0|1|1|1|2|0|1|0|1|1|1;AF_Male=3.77729e-05;AF_AFR=9.23483e-04;AC_raw=15;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=8.25294e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36291e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=14;AC_AFR=14;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:0.0001096,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=K/R,HGVSp=ENSP00000468424.1:p.Lys127Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,EA_MAF=G:0.0014,Allele=G,IMPACT=MODERATE,EXON=4/13,ExAC_AMR_MAF=G:0.001254,cDNA_position=511,CDS_position=380,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs144433221,VARIANT_CLASS=SNV,Protein_position=127,Codons=aAg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:1.071e-04,HGVSc=ENST00000592782.1:c.380A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	523	523	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-43;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06782e-06;Hom=0;AF_POPMAX=3.24950e-05;AN_POPMAX=30774;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42677e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.40426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24950e-05;AS_RF=7.83979e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/E,HGVSp=ENSP00000468424.1:p.Val131Glu,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=5/13,cDNA_position=523,CDS_position=392,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=131,Codons=gTg/gAg,MINIMISED=1,HGVSc=ENST00000592782.1:c.392T>A
CDS|ENST00000592782	VCF	missense_variant	534	534	0.0	.	.	AC_Male=1;AF_NFE=1.79398e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-64;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13028e-06;Hom=0;AF_POPMAX=1.79398e-05;AN_POPMAX=111484;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0;AF_Male=7.42148e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.25373e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=67;AF_Female=8.98876e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13408e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.657e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.015e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.011),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=H/Y,HGVSp=ENSP00000468424.1:p.His135Tyr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=5/13,ExAC_AMR_MAF=T:0,cDNA_position=534,CDS_position=403,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs753759265,VARIANT_CLASS=SNV,Protein_position=135,Codons=Cat/Tat,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.403C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	543	543	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-36;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21939e-05;Hom=0;AF_POPMAX=1.15969e-04;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AF_Male=7.42027e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.77324e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=1.79762e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=3.24907e-05;AS_RF=8.84156e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.15969e-04;AC_SAS=1;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.272e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.111),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/M,HGVSp=ENSP00000468424.1:p.Val138Met,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=5/13,ExAC_AMR_MAF=A:0,cDNA_position=543,CDS_position=412,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs752448187,VARIANT_CLASS=SNV,Protein_position=138,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592782.1:c.412G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	549	549	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-75;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06372e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.15584e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=8.98521e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.41661e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.265e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.025),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000468424.1:p.Pro140Ser,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=5/13,ExAC_AMR_MAF=T:0,cDNA_position=549,CDS_position=418,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs758111913,VARIANT_CLASS=SNV,Protein_position=140,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.418C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	550	550	0.0	.	.	AC_Male=0;AF_NFE=8.96363e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-36;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06355e-06;Hom=0;AF_POPMAX=8.96363e-06;AN_POPMAX=111562;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41176e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00024e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.032),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000468424.1:p.Pro140Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=5/13,cDNA_position=550,CDS_position=419,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=140,Codons=cCt/cTt,MINIMISED=1,HGVSc=ENST00000592782.1:c.419C>T
CDS|ENST00000592782	VCF	missense_variant	552	552	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-72;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21915e-05;Hom=0;AF_POPMAX=1.73933e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|1|0|0|0|1|0|0|0|0|0|0;AF_Male=1.48381e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.76190e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98586e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=3;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.73933e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.29),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=A:0,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=missense_variant,GMAF=A:0.0002,ExAC_SAS_MAF=A:0,SOMATIC=0&1,IMPACT=MODERATE,ExAC_AMR_MAF=A:0,CDS_position=421,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs201386803&COSM349346,VARIANT_CLASS=SNV,Protein_position=141,AA_MAF=A:0,Codons=Gac/Aac,ExAC_Adj_MAF=A:0,PHENO=0&1,ExAC_EAS_MAF=A:1.653e-05,BIOTYPE=protein_coding,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EUR_MAF=A:0.001,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.015),ExAC_FIN_MAF=A:0.0002313,ENSP=ENSP00000468424,Amino_acids=D/N,HGVSp=ENSP00000468424.1:p.Asp141Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,EXON=5/13,cDNA_position=552,SAS_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592782.1:c.421G>A
CDS|ENST00000592782	VCF	missense_variant	573	573	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-54;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62509e-05;Hom=0;AF_POPMAX=1.19119e-04;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|2|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41697e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.40000e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=2.69508e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99062e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=1.19119e-04;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.736),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000468424.1:p.Glu148Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=5/13,cDNA_position=573,CDS_position=442,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=148,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000592782.1:c.442G>A
CDS|ENST00000592782	VCF	missense_variant	576	576	0.0	.	.	AC_Male=1;AF_NFE=8.96106e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-53;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06296e-06;Hom=0;AF_POPMAX=8.96106e-06;AN_POPMAX=111594;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41730e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.46809e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00924e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.932),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000468424.1:p.Pro149Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=5/13,cDNA_position=576,CDS_position=445,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=149,Codons=Ccc/Gcc,MINIMISED=1,HGVSc=ENST00000592782.1:c.445C>G
CDS|ENST00000592782	VCF	missense_variant	594	594	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-51;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06398e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41917e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=3.27293e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.08),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.369),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000468424.1:p.Gly155Ser,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=5/13,cDNA_position=594,CDS_position=463,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=155,Codons=Ggc/Agc,MINIMISED=1,HGVSc=ENST00000592782.1:c.463G>A
CDS|ENST00000592782	VCF	missense_variant	624	624	0.0	.	.	AC_Male=12;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|0|2|2|2|2|6|13|4|3|2|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.90310e-58;AF_OTH=5.47445e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=3;Hom_Male=0;AC=37;Hom_NFE=0;AF=1.50482e-04;Hom=0;AF_POPMAX=2.09150e-03;AN_POPMAX=15300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|3|2|6|4|8|3|1|3|0|1|1|1|0|2|0|1;AF_Male=8.91080e-05;AF_AFR=2.09150e-03;AC_raw=38;AB_MEDIAN=4.66288e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=2.24804e-04;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|36;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44169e-01;Hom_AMR=0;AC_EAS=0;AC_Female=25;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=32;AC_AFR=32;Hom_SAS=0;AC_ASJ=0;AF_raw=1.54302e-04;Hom_Female=0;AF_AMR=5.95841e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.66),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=A:0.003,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=A:0.0014,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=missense_variant,GMAF=A:0.0010,ExAC_SAS_MAF=A:0,IMPACT=MODERATE,ExAC_AMR_MAF=A:0.002214,CDS_position=493,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs149737135,VARIANT_CLASS=SNV,Protein_position=165,AA_MAF=A:0,Codons=Gat/Aat,ExAC_Adj_MAF=A:8.655e-05,ExAC_EAS_MAF=A:0.0001983,ExAC_MAF=A:0,BIOTYPE=protein_coding,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Amino_acids=D/N,HGVSp=ENSP00000468424.1:p.Asp165Asn,STRAND=1,CCDS=CCDS11494.1,EA_MAF=A:0.003,Allele=A,EXON=5/13,cDNA_position=624,SAS_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:1.977e-04,HGVSc=ENST00000592782.1:c.493G>A
CDS|ENST00000592782	VCF	missense_variant	627	627	0.0	.	.	AC_Male=0;AF_NFE=8.98101e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-44;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13524e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.33333e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=1.79863e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19608e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.264e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.503e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.206),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/C,HGVSp=ENSP00000468424.1:p.Arg166Cys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=5/13,ExAC_AMR_MAF=T:0,cDNA_position=627,CDS_position=496,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778948844&COSM3518200,VARIANT_CLASS=SNV,Protein_position=166,Codons=Cgt/Tgt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.496C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	628	628	0.0	.	.	AC_Male=1;AF_NFE=1.79614e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-60;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13557e-06;Hom=0;AF_POPMAX=1.79614e-05;AN_POPMAX=111350;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.42721e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.70100e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=8.99329e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19786e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.264e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.503e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/P,HGVSp=ENSP00000468424.1:p.Arg166Pro,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=5/13,ExAC_AMR_MAF=C:0,cDNA_position=628,CDS_position=497,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs748432196,VARIANT_CLASS=SNV,Protein_position=166,Codons=cGt/cCt,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.497G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	633	633	0.0	.	.	AC_Male=1;AF_NFE=2.69624e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-79;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22082e-05;Hom=0;AF_POPMAX=2.69624e-05;AN_POPMAX=111266;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43075e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.43709e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=51;AF_Female=1.79921e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.11),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.27e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.504e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.801),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=V/M,HGVSp=ENSP00000468424.1:p.Val168Met,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=5/13,ExAC_AMR_MAF=A:0,cDNA_position=633,CDS_position=502,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs773364852,VARIANT_CLASS=SNV,Protein_position=168,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.502G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	712	712	0.0	.	.	AC_Male=0;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-62;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=55;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99132e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.411),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/Q,HGVSp=ENSP00000468424.1:p.Pro194Gln,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=6/13,ExAC_AMR_MAF=T:0,cDNA_position=712,CDS_position=581,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,Protein_position=194,Codons=cCg/cAg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.581C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	712	712	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-188;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=145;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.99177e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.177),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000468424.1:p.Pro194Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=6/13,ExAC_AMR_MAF=T:0,cDNA_position=712,CDS_position=581,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,Protein_position=194,Codons=cCg/cTg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.581C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	714	714	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-146;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.64198e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=162;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.16858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.638),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000468424.1:p.Glu195Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=6/13,cDNA_position=714,CDS_position=583,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=195,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000592782.1:c.583G>A
CDS|ENST00000592782	VCF	missense_variant	715	715	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-92;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=74;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.247),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/A,HGVSp=ENSP00000468424.1:p.Glu195Ala,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=6/13,cDNA_position=715,CDS_position=584,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=195,Codons=gAg/gCg,MINIMISED=1,HGVSc=ENST00000592782.1:c.584A>C
CDS|ENST00000592782	VCF	missense_variant	735	735	0.0	.	.	AC_Male=0;AF_NFE=8.96282e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-295;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06345e-06;Hom=0;AF_POPMAX=8.96282e-06;AN_POPMAX=111572;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51327e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=226;AF_Female=8.98763e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.243e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.96),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/W,HGVSp=ENSP00000468424.1:p.Arg202Trp,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=T:0,cDNA_position=735,CDS_position=604,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764148755,VARIANT_CLASS=SNV,Protein_position=202,Codons=Cgg/Tgg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.604C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	736	736	0.0	.	.	AC_Male=35;AF_NFE=1.07544e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|9|11|10|12|4|2|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-103;AF_OTH=1.82415e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=49;Hom_NFE=0;AF=1.99100e-04;Hom=0;AF_POPMAX=2.23441e-03;AN_POPMAX=9846;AC_NFE=12;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|4|3|1|2|1|6|7|4|4|0|2|1;AF_Male=2.59586e-04;AF_AFR=0.00000e+00;AC_raw=49;AB_MEDIAN=4.65116e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=2.23441e-03;DP_MEDIAN=74;AF_Female=1.25811e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|49;Hom_raw=0;AF_SAS=3.89838e-04;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=14;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=12;POPMAX=ASJ;AC_POPMAX=22;AC_AFR=0;Hom_SAS=0;AC_ASJ=22;AF_raw=1.98967e-04;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.85),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:0.0002225,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0002,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0002699,AFR_MAF=A:0.0005453,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.023),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/Q,HGVSp=ENSP00000468424.1:p.Arg202Gln,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=A:0,cDNA_position=736,CDS_position=605,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs150418753&COSM4067023,VARIANT_CLASS=SNV,Protein_position=202,Codons=cGg/cAg,MINIMISED=1,ExAC_AFR_MAF=A:2.224e-04,HGVSc=ENST00000592782.1:c.605G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	744	744	0.0	.	.	AC_Male=5;AF_NFE=1.25390e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|2|3|9|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-94;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=17;Hom_NFE=0;AF=6.90524e-05;Hom=0;AF_POPMAX=1.25390e-04;AN_POPMAX=111652;AC_NFE=14;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|0|1|1|1|2|0|2|2|0|1|0|1|0|0;AF_Male=3.70749e-05;AF_AFR=0.00000e+00;AC_raw=17;AB_MEDIAN=5.09033e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=64;AF_Female=1.07790e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|17;Hom_raw=0;AF_SAS=9.74596e-05;AS_RF=9.36765e-01;Hom_AMR=0;AC_EAS=0;AC_Female=12;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=NFE;AC_POPMAX=14;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.90294e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:5.768e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:7.495e-05,AFR_MAF=A:0.0001211,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.821),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000468424.1:p.Gly205Ser,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=A:0,cDNA_position=744,CDS_position=613,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs781499966,VARIANT_CLASS=SNV,Protein_position=205,Codons=Ggc/Agc,MINIMISED=1,ExAC_AFR_MAF=A:5.765e-05,HGVSc=ENST00000592782.1:c.613G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	749	749	0.0	.	.	AC_Male=1;AF_NFE=3.58230e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-225;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62467e-05;Hom=0;AF_POPMAX=3.58230e-05;AN_POPMAX=111660;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.41499e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55048e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=196;AF_Female=2.69440e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:5.996e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.281),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=W/C,HGVSp=ENSP00000468424.1:p.Trp206Cys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=T:0,cDNA_position=749,CDS_position=618,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs746041079,VARIANT_CLASS=SNV,Protein_position=206,Codons=tgG/tgT,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000592782.1:c.618G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	750	750	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-212;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06141e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.11392e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=158;AF_Female=8.98134e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08869e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.41),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.016),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000468424.1:p.Leu207Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=G:0,cDNA_position=750,CDS_position=619,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756018179,VARIANT_CLASS=SNV,Protein_position=207,Codons=Ctc/Gtc,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.619C>G,ExAC_Adj_MAF=G:8.639e-05
CDS|ENST00000592782	VCF	missense_variant	754	754	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|1|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-130;AF_OTH=1.82282e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03062e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|1|1|0|0|0|0;AF_Male=1.48278e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=76;AF_Female=2.69426e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.39678e-01;Hom_AMR=0;AC_EAS=4;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.43),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.043),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000468424.1:p.Pro208Leu,STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=A:0&T:0,cDNA_position=754,CDS_position=623,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,Protein_position=208,Codons=cCc/cTc,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000592782.1:c.623C>T,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000592782	VCF	missense_variant	754	754	0.0	.	.	AC_Male=1;AF_NFE=8.95415e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-239;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21837e-05;Hom=0;AF_POPMAX=5.95557e-05;AN_POPMAX=33582;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.31915e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=153;AF_Female=1.79617e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.48089e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.873),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/H,HGVSp=ENSP00000468424.1:p.Pro208His,STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=A:0&T:0,cDNA_position=754,CDS_position=623,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,Protein_position=208,Codons=cCc/cAc,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000592782.1:c.623C>A,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000592782	VCF	missense_variant	780	780	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-238;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.42254e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=142;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.49406e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.24),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.499e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000468424.1:p.Val217Leu,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=C:0,cDNA_position=780,CDS_position=649,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs774095582,VARIANT_CLASS=SNV,Protein_position=217,Codons=Gtc/Ctc,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.649G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	789	789	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-102;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.59375e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=7.94592e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.687),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/W,HGVSp=ENSP00000468424.1:p.Arg220Trp,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=7/13,cDNA_position=789,CDS_position=658,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=220,Codons=Cgg/Tgg,MINIMISED=1,HGVSc=ENST00000592782.1:c.658C>T
CDS|ENST00000592782	VCF	missense_variant	790	790	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-67;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21820e-05;Hom=0;AF_POPMAX=1.01523e-04;AN_POPMAX=9850;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.62963e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=1.01523e-04;DP_MEDIAN=51;AF_Female=1.79601e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.12),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.498e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/Q,HGVSp=ENSP00000468424.1:p.Arg220Gln,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=A:0,cDNA_position=790,CDS_position=659,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs771441667,VARIANT_CLASS=SNV,Protein_position=220,Codons=cGg/cAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.659G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	818	818	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-165;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95159e-06;AN_POPMAX=111712;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.56897e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=116;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17542e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.928),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=I/M,HGVSp=ENSP00000468424.1:p.Ile229Met,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,EA_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=G:0,cDNA_position=818,CDS_position=687,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs375089291,VARIANT_CLASS=SNV,Protein_position=229,Codons=atC/atG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.687C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	832	832	0.0	.	.	AC_Male=1;AF_NFE=1.79054e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-248;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12196e-06;Hom=0;AF_POPMAX=1.79054e-05;AN_POPMAX=111698;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41312e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.99184e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=192;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.647e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=H/R,HGVSp=ENSP00000468424.1:p.His234Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=G:0,cDNA_position=832,CDS_position=701,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs775829411,VARIANT_CLASS=SNV,Protein_position=234,Codons=cAt/cGt,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.701A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	838	838	0.0	.	.	AC_Male=0;AF_NFE=8.95399e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-226;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06124e-06;Hom=0;AF_POPMAX=8.95399e-06;AN_POPMAX=111682;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.30168e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=179;AF_Female=8.98150e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.22854e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.96),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=Y/C,HGVSp=ENSP00000468424.1:p.Tyr236Cys,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=G:0,cDNA_position=838,CDS_position=707,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763238851,VARIANT_CLASS=SNV,Protein_position=236,Codons=tAt/tGt,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.707A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	844	844	0.0	.	.	AC_Male=0;AF_NFE=8.95592e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06167e-06;Hom=0;AF_POPMAX=8.95592e-06;AN_POPMAX=111658;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=8.98198e-06;GQ_HIST_ALT=0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.79803e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=T/K,HGVSp=ENSP00000468424.1:p.Thr238Lys,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/13,ExAC_AMR_MAF=A:0,cDNA_position=844,CDS_position=713,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764674925,VARIANT_CLASS=SNV,Protein_position=238,Codons=aCa/aAa,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.713C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	853	853	0.0	.	.	AC_Male=0;AF_NFE=8.97102e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-130;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06573e-06;Hom=0;AF_POPMAX=8.97102e-06;AN_POPMAX=111470;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.86905e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=168;AF_Female=8.98957e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.27e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.125),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=K/M,HGVSp=ENSP00000468424.1:p.Lys241Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=T:0,cDNA_position=853,CDS_position=722,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs758261924,VARIANT_CLASS=SNV,Protein_position=241,Codons=aAg/aTg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.722A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	855	855	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|3|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-55;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62617e-05;Hom=0;AF_POPMAX=1.19133e-04;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48449e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.74078e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=1.79775e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.92315e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=1.19133e-04;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.653e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.089),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/V,HGVSp=ENSP00000468424.1:p.Met242Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=G:0,cDNA_position=855,CDS_position=724,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs777621617,VARIANT_CLASS=SNV,Protein_position=242,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.724A>G,ExAC_Adj_MAF=G:0.0001728
CDS|ENST00000592782	VCF	missense_variant	895	895	0.0	.	.	AC_Male=1;AF_NFE=8.95319e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-214;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12216e-06;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41334e-06;AF_AFR=6.53424e-05;AC_raw=2;AB_MEDIAN=4.72222e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=180;AF_Female=8.98085e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.48607e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(1),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/H,HGVSp=ENSP00000468424.1:p.Arg255His,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=895,CDS_position=764,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746537411,VARIANT_CLASS=SNV,Protein_position=255,Codons=cGt/cAt,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592782.1:c.764G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	912	912	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-66;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.42413e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.997),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000468424.1:p.Pro261Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=8/13,cDNA_position=912,CDS_position=781,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=261,Codons=Cca/Gca,MINIMISED=1,HGVSc=ENST00000592782.1:c.781C>G
CDS|ENST00000592782	VCF	missense_variant	957	957	0.0	.	.	AC_Male=2;AF_NFE=1.79067e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|2|0|0|1|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=3.98107e-153;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=1.34541e-04;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03059e-05;Hom=0;AF_POPMAX=1.34541e-04;AN_POPMAX=22298;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;AF_Male=1.48262e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.69880e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=2.69450e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.45888e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.2),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:4.119e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.076),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000468424.1:p.Ile276Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,EA_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=G:0,cDNA_position=957,CDS_position=826,ExAC_NFE_MAF=G:0.0004536,SYMBOL=NMT1,Existing_variation=rs371122860,VARIANT_CLASS=SNV,Protein_position=276,Codons=Atc/Gtc,MINIMISED=1,ExAC_AFR_MAF=G:4.118e-05,HGVSc=ENST00000592782.1:c.826A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	969	969	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-165;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06190e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.83051e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=118;AF_Female=8.98343e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53015e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.982),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/F,HGVSp=ENSP00000468424.1:p.Val280Phe,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=T:0,cDNA_position=969,CDS_position=838,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772467109,VARIANT_CLASS=SNV,Protein_position=280,Codons=Gtt/Ttt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.838G>T,ExAC_Adj_MAF=T:8.64e-05
CDS|ENST00000592782	VCF	missense_variant	978	978	0.0	.	.	AC_Male=1;AF_NFE=8.96266e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-105;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06312e-06;Hom=0;AF_POPMAX=8.96266e-06;AN_POPMAX=111574;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41587e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.93750e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=64;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.78341e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.793),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000468424.1:p.Ala283Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=8/13,cDNA_position=978,CDS_position=847,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=283,Codons=Gcc/Acc,MINIMISED=1,HGVSc=ENST00000592782.1:c.847G>A
CDS|ENST00000592782	VCF	missense_variant	982	982	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=6.30957e-128;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=4.48471e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06345e-06;Hom=0;AF_POPMAX=4.48471e-05;AN_POPMAX=22298;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41642e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.81013e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54228e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.24e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.988),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/E,HGVSp=ENSP00000468424.1:p.Gly284Glu,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=A:0,cDNA_position=982,CDS_position=851,ExAC_NFE_MAF=A:0.0001512,SYMBOL=NMT1,Existing_variation=rs766531390,VARIANT_CLASS=SNV,Protein_position=284,Codons=gGg/gAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.851G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	990	990	0.0	.	.	AC_Male=1;AF_NFE=1.79482e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-61;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21973e-05;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|1|0|0|0|0|1|1|0|0|0|0;AF_Male=7.42027e-06;AF_AFR=6.53424e-05;AC_raw=4;AB_MEDIAN=4.60242e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.79872e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.84998e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.0001212,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.428),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/I,HGVSp=ENSP00000468424.1:p.Leu287Ile,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=G:0,cDNA_position=990,CDS_position=859,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759663986,VARIANT_CLASS=SNV,Protein_position=287,Codons=Cta/Ata,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.859C>A,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	990	990	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-71;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21973e-05;Hom=0;AF_POPMAX=9.74659e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|1|1|0|0|0|0|0|0|0;AF_Male=2.22608e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.83333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=57;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=9.74659e-05;AS_RF=8.84998e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.0001212,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.55),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000468424.1:p.Leu287Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=G:0,cDNA_position=990,CDS_position=859,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759663986,VARIANT_CLASS=SNV,Protein_position=287,Codons=Cta/Gta,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.859C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1002	1002	0.0	.	.	AC_Male=3;AF_NFE=2.70032e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|1|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-77;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.85053e-05;Hom=0;AF_POPMAX=1.96053e-04;AN_POPMAX=15302;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|1|0|1|0|1|0|1|1|1|1|0|0|0;AF_Male=2.22962e-05;AF_AFR=1.96053e-04;AC_raw=8;AB_MEDIAN=4.87441e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=3.60308e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51581e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=3;AC_AFR=3;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.35),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:3.303e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/I,HGVSp=ENSP00000468424.1:p.Val291Ile,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0002,Allele=A,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=A:0.000289,cDNA_position=1002,CDS_position=871,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs376218058,VARIANT_CLASS=SNV,Protein_position=291,Codons=Gtt/Att,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000592782.1:c.871G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1006	1006	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-153;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07382e-06;Hom=0;AF_POPMAX=2.97992e-05;AN_POPMAX=33558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.13889e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=72;AF_Female=9.01015e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92885e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.264e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.552),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/V,HGVSp=ENSP00000468424.1:p.Gly292Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=8/13,ExAC_AMR_MAF=T:0,cDNA_position=1006,CDS_position=875,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764042790,VARIANT_CLASS=SNV,Protein_position=292,Codons=gGc/gTc,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.875G>T,ExAC_Adj_MAF=T:8.658e-05
CDS|ENST00000592782	VCF	missense_variant	1041	1041	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-132;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.94949e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.04140e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.927),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/W,HGVSp=ENSP00000468424.1:p.Arg304Trp,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/13,cDNA_position=1041,CDS_position=910,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=304,Codons=Cgg/Tgg,MINIMISED=1,HGVSc=ENST00000592782.1:c.910C>T
CDS|ENST00000592782	VCF	missense_variant	1084	1084	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-79;AF_OTH=1.82349e-04;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06131e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.15730e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=8.98118e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.21292e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.625),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000468424.1:p.Met318Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/13,cDNA_position=1084,CDS_position=953,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=318,Codons=aTg/aGg,MINIMISED=1,HGVSc=ENST00000592782.1:c.953T>G
CDS|ENST00000592782	VCF	missense_variant	1102	1102	0.0	.	.	AC_Male=1;AF_NFE=8.95672e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-104;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06187e-06;Hom=0;AF_POPMAX=8.95672e-06;AN_POPMAX=111648;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.41455e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.47059e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=85;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51581e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.024),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000468424.1:p.Met324Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/13,cDNA_position=1102,CDS_position=971,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=324,Codons=aTg/aGg,MINIMISED=1,HGVSc=ENST00000592782.1:c.971T>G
CDS|ENST00000592782	VCF	missense_variant	1113	1113	0.0	.	.	AC_Male=1;AF_NFE=8.96523e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-50;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06385e-06;Hom=0;AF_POPMAX=8.96523e-06;AN_POPMAX=111542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41807e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=48;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.25808e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.68),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/G,HGVSp=ENSP00000468424.1:p.Arg328Gly,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/13,cDNA_position=1113,CDS_position=982,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=328,Codons=Cga/Gga,MINIMISED=1,HGVSc=ENST00000592782.1:c.982C>G
CDS|ENST00000592782	VCF	missense_variant	1119	1119	0.0	.	.	AC_Male=1;AF_NFE=8.96877e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-100;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06481e-06;Hom=0;AF_POPMAX=8.96877e-06;AN_POPMAX=111498;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.42005e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.02299e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=87;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18859e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.952),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/T,HGVSp=ENSP00000468424.1:p.Pro330Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/13,cDNA_position=1119,CDS_position=988,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=330,Codons=Cca/Aca,MINIMISED=1,HGVSc=ENST00000592782.1:c.988C>A
CDS|ENST00000592782	VCF	missense_variant	1125	1125	0.0	.	.	AC_Male=1;AF_NFE=1.80505e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-37;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.17702e-06;Hom=0;AF_POPMAX=1.80505e-05;AN_POPMAX=110800;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46614e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.08333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=9.03751e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.31706e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.9),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.253e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.649e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=T/A,HGVSp=ENSP00000468424.1:p.Thr332Ala,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=G:0,cDNA_position=1125,CDS_position=994,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767459640,VARIANT_CLASS=SNV,Protein_position=332,Codons=Act/Gct,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.994A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1126	1126	0.0	.	.	AC_Male=1;AF_NFE=1.80470e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-36;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22639e-05;Hom=0;AF_POPMAX=2.98900e-05;AN_POPMAX=33456;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46480e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.21739e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=1.80737e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.04452e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=2.98900e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.77),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.193e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.64e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=T/S,HGVSp=ENSP00000468424.1:p.Thr332Ser,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=G:0,cDNA_position=1126,CDS_position=995,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750330678,VARIANT_CLASS=SNV,Protein_position=332,Codons=aCt/aGt,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.995C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1126	1126	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=69;AB_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.99950e-05;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08797e-06;Hom=0;AF_POPMAX=5.80990e-05;AN_POPMAX=17212;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.57576e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=9.03685e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.47224e-02;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80990e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.43),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.193e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.64e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=T/N,HGVSp=ENSP00000468424.1:p.Thr332Asn,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=G:0,cDNA_position=1126,CDS_position=995,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750330678,VARIANT_CLASS=SNV,Protein_position=332,Codons=aCt/aAt,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.995C>A,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1135	1135	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-50;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07515e-06;Hom=0;AF_POPMAX=6.54365e-05;AN_POPMAX=15282;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.54365e-05;AC_raw=1;AB_MEDIAN=5.14286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.01015e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.07823e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.114),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/I,HGVSp=ENSP00000468424.1:p.Thr335Ile,STRAND=1,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=10/13,cDNA_position=1135,CDS_position=1004,SYMBOL=NMT1,Existing_variation=rs375623297,VARIANT_CLASS=SNV,Protein_position=335,Codons=aCa/aTa,MINIMISED=1,HGVSc=ENST00000592782.1:c.1004C>T
CDS|ENST00000592782	VCF	missense_variant	1137	1137	0.0	.	.	AC_Male=2;AF_NFE=5.39035e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|1|0|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-36;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44328e-05;Hom=0;AF_POPMAX=5.39035e-05;AN_POPMAX=111310;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|2|0|0|0|2|1|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48683e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.59567e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=3.60172e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08070e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.06),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.734e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.116e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000468424.1:p.Ala336Thr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=A:0,cDNA_position=1137,CDS_position=1006,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs760138330,VARIANT_CLASS=SNV,Protein_position=336,Codons=Gct/Act,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592782.1:c.1006G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1152	1152	0.0	.	.	AC_Male=2;AF_NFE=2.68846e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-62;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21914e-05;Hom=0;AF_POPMAX=2.68846e-05;AN_POPMAX=111588;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0|0;AF_Male=1.48381e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=8.98569e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44503e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.332e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.51e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.83),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/V,HGVSp=ENSP00000468424.1:p.Met341Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=G:0,cDNA_position=1152,CDS_position=1021,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs554809034,VARIANT_CLASS=SNV,Protein_position=341,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.1021A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1170	1170	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-44;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06144e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.36055e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.07),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.059),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000468424.1:p.Pro347Ser,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/13,cDNA_position=1170,CDS_position=1039,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=347,Codons=Cca/Tca,HGVSc=ENST00000592782.1:c.1039C>T
CDS|ENST00000592782	VCF	missense_variant	1170	1170	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-78;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06144e-06;Hom=0;AF_POPMAX=2.97885e-05;AN_POPMAX=33570;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.09434e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=8.98182e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40992e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97885e-05;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.17),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000468424.1:p.Pro347Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/13,cDNA_position=1170,CDS_position=1039,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=347,Codons=Cca/Gca,HGVSc=ENST00000592782.1:c.1039C>G
CDS|ENST00000592782	VCF	missense_variant	1173	1173	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-36;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12236e-06;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=1.48269e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.07246e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=8.81705e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.08),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:1.651e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0.0001214,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000468424.1:p.Val348Leu,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=C:0,cDNA_position=1173,CDS_position=1042,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs753488937,VARIANT_CLASS=SNV,Protein_position=348,Codons=Gta/Cta,MINIMISED=1,ExAC_AFR_MAF=C:1.647e-05,HGVSc=ENST00000592782.1:c.1042G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	missense_variant	1179	1179	0.0	.	.	AC_Male=1;AF_NFE=8.95303e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-80;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06118e-06;Hom=0;AF_POPMAX=8.95303e-06;AN_POPMAX=111694;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.41334e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.74576e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=59;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50356e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.249e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.039),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=H/Y,HGVSp=ENSP00000468424.1:p.His350Tyr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=T:0,cDNA_position=1179,CDS_position=1048,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754671896,VARIANT_CLASS=SNV,Protein_position=350,Codons=Cac/Tac,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1048C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1185	1185	0.0	.	.	AC_Male=0;AF_NFE=1.79048e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-108;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12203e-06;Hom=0;AF_POPMAX=1.79048e-05;AN_POPMAX=111702;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.21263e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=1.79617e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:2.999e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.883),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/F,HGVSp=ENSP00000468424.1:p.Leu352Phe,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=T:0,cDNA_position=1185,CDS_position=1054,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778639871,VARIANT_CLASS=SNV,Protein_position=352,Codons=Ctc/Ttc,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.1054C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1195	1195	0.0	.	.	AC_Male=2;AF_NFE=3.58083e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|1|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-87;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03044e-05;Hom=0;AF_POPMAX=3.58083e-05;AN_POPMAX=111706;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|2|1|0|1|0|0;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=74;AF_Female=2.69416e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.179),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/M,HGVSp=ENSP00000468424.1:p.Arg355Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=T:0,cDNA_position=1195,CDS_position=1064,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757647993,VARIANT_CLASS=SNV,Protein_position=355,Codons=aGg/aTg,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000592782.1:c.1064G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1195	1195	0.0	.	.	AC_Male=1;AF_NFE=8.95207e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-75;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06088e-06;Hom=0;AF_POPMAX=8.95207e-06;AN_POPMAX=111706;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.10204e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=49;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.89),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=R/K,HGVSp=ENSP00000468424.1:p.Arg355Lys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/13,ExAC_AMR_MAF=T:0,cDNA_position=1195,CDS_position=1064,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757647993,VARIANT_CLASS=SNV,Protein_position=355,Codons=aGg/aAg,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000592782.1:c.1064G>A,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1202	1202	0.0	.	.	AC_Male=0;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-113;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=8.95159e-06;AN_POPMAX=111712;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.12195e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=82;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.737),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/F,HGVSp=ENSP00000468424.1:p.Leu357Phe,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=10/13,cDNA_position=1202,CDS_position=1071,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=357,Codons=ttG/ttC,MINIMISED=1,HGVSc=ENST00000592782.1:c.1071G>C
CDS|ENST00000592782	VCF	missense_variant	1219	1219	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.03025e-26;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12170e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=7.49951e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=1;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.95),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/M,HGVSp=ENSP00000468424.1:p.Thr363Met,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/13,cDNA_position=1219,CDS_position=1088,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=363,Codons=aCg/aTg,MINIMISED=1,HGVSc=ENST00000592782.1:c.1088C>T
CDS|ENST00000592782	VCF	missense_variant	1224	1224	0.0	.	.	AC_Male=18;AF_NFE=1.79035e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|5|11|3|6|4|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.31311e-75;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=32;Hom_NFE=0;AF=1.29949e-04;Hom=0;AF_POPMAX=1.89493e-03;AN_POPMAX=15304;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|2|4|2|4|0|1|2|0|1|0|2|0|3|0;AF_Male=1.33436e-04;AF_AFR=1.89493e-03;AC_raw=32;AB_MEDIAN=4.44496e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=68;AF_Female=1.25725e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|32;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44873e-01;Hom_AMR=0;AC_EAS=0;AC_Female=14;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=29;AC_AFR=29;Hom_SAS=0;AC_ASJ=0;AF_raw=1.29938e-04;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.29),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=A:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=A:0.0014,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=missense_variant,GMAF=A:0.0004,ExAC_SAS_MAF=A:0,IMPACT=MODERATE,ExAC_AMR_MAF=A:0.001538,CDS_position=1093,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs148483868,VARIANT_CLASS=SNV,Protein_position=365,AA_MAF=A:0,Codons=Gtc/Atc,ExAC_Adj_MAF=A:8.637e-05,ExAC_EAS_MAF=A:0.0001401,ExAC_MAF=A:0,BIOTYPE=protein_coding,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Amino_acids=V/I,HGVSp=ENSP00000468424.1:p.Val365Ile,STRAND=1,CCDS=CCDS11494.1,EA_MAF=A:0.0014,Allele=A,EXON=10/13,cDNA_position=1224,SAS_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:1.400e-04,HGVSc=ENST00000592782.1:c.1093G>A
CDS|ENST00000592782	VCF	missense_variant	1225	1225	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-74;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06088e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41301e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.61538e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=65;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.01512e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.3),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.02),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/D,HGVSp=ENSP00000468424.1:p.Val365Asp,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/13,cDNA_position=1225,CDS_position=1094,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=365,Codons=gTc/gAc,MINIMISED=1,HGVSc=ENST00000592782.1:c.1094T>A
CDS|ENST00000592782	VCF	missense_variant	1245	1245	0.0	.	.	AC_Male=1;AF_NFE=8.95223e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-19;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06128e-06;Hom=0;AF_POPMAX=8.95223e-06;AN_POPMAX=111704;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41400e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.13018e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.56),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.011),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000468424.1:p.Glu372Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/13,cDNA_position=1245,CDS_position=1114,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=372,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000592782.1:c.1114G>A
CDS|ENST00000592782	VCF	missense_variant	1260	1260	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=2;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.86863e-01;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.25000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.71630e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.781),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000468424.1:p.Pro377Ser,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/13,cDNA_position=1260,CDS_position=1129,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=377,Codons=Ccc/Tcc,MINIMISED=1,HGVSc=ENST00000592782.1:c.1129C>T
CDS|ENST00000592782	VCF	missense_variant	1272	1272	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-82;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06342e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41774e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.13636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41631e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000468424.1:p.Ile381Val,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/13,cDNA_position=1272,CDS_position=1141,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=381,Codons=Atc/Gtc,MINIMISED=1,HGVSc=ENST00000592782.1:c.1141A>G
CDS|ENST00000592782	VCF	missense_variant	1278	1278	0.0	.	.	AC_Male=1;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-23;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06527e-06;Hom=0;AF_POPMAX=8.96379e-06;AN_POPMAX=111560;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42082e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.64592e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.15),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.07),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=D/N,HGVSp=ENSP00000468424.1:p.Asp383Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/13,cDNA_position=1278,CDS_position=1147,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=383,Codons=Gac/Aac,MINIMISED=1,HGVSc=ENST00000592782.1:c.1147G>A
CDS|ENST00000592782	VCF	missense_variant	1284	1284	0.0	.	.	AC_Male=0;AF_NFE=8.96716e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-48;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06646e-06;Hom=0;AF_POPMAX=8.96716e-06;AN_POPMAX=111518;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.63415e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=8.99313e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19983e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.907),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=F/I,HGVSp=ENSP00000468424.1:p.Phe385Ile,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/13,cDNA_position=1284,CDS_position=1153,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=385,Codons=Ttc/Atc,HGVSc=ENST00000592782.1:c.1153T>A
CDS|ENST00000592782	VCF	missense_variant	1284	1284	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=62;AB_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.57615e-03;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06646e-06;Hom=0;AF_POPMAX=5.79845e-05;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42291e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.44512e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.08515e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79845e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.749),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=F/L,HGVSp=ENSP00000468424.1:p.Phe385Leu,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=10/13,cDNA_position=1284,CDS_position=1153,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=385,Codons=Ttc/Ctc,HGVSc=ENST00000592782.1:c.1153T>C
CDS|ENST00000592782	VCF	missense_variant	1290	1290	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-27;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06967e-06;Hom=0;AF_POPMAX=3.25500e-05;AN_POPMAX=30722;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42810e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25500e-05;AS_RF=8.45900e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.172),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000468424.1:p.Val387Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/13,cDNA_position=1290,CDS_position=1159,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=387,Codons=Gtg/Ttg,MINIMISED=1,HGVSc=ENST00000592782.1:c.1159G>T
CDS|ENST00000592782	VCF	missense_variant	1295	1295	0.0	.	.	AC_Male=0;AF_NFE=8.99119e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-13;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07445e-06;Hom=0;AF_POPMAX=8.99119e-06;AN_POPMAX=111220;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=10;AF_Female=9.01242e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=5.86404e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.226),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=E/D,HGVSp=ENSP00000468424.1:p.Glu388Asp,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=10/13,cDNA_position=1295,CDS_position=1164,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=388,Codons=gaG/gaC,MINIMISED=1,HGVSc=ENST00000592782.1:c.1164G>C
CDS|ENST00000592782	VCF	missense_variant	1297	1297	0.0	.	.	AC_Male=1;AF_NFE=9.07935e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-136;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10806e-06;Hom=0;AF_POPMAX=9.07935e-06;AN_POPMAX=110140;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.50413e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57447e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06919e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.73),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=N/S,HGVSp=ENSP00000468424.1:p.Asn389Ser,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/13,cDNA_position=1297,CDS_position=1166,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=389,Codons=aAc/aGc,MINIMISED=1,HGVSc=ENST00000592782.1:c.1166A>G
CDS|ENST00000592782	VCF	missense_variant	1299	1299	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-88;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10590e-06;Hom=0;AF_POPMAX=3.28947e-05;AN_POPMAX=30400;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.49895e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.91803e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.28947e-05;AS_RF=9.51545e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.41),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.487e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000468424.1:p.Ala390Thr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1299,CDS_position=1168,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749387380,VARIANT_CLASS=SNV,Protein_position=390,Codons=Gca/Aca,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1168G>A,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1299	1299	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-224;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10590e-06;Hom=0;AF_POPMAX=3.28947e-05;AN_POPMAX=30400;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.26136e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=176;AF_Female=9.07441e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.28947e-05;AS_RF=9.51545e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.94),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.487e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/S,HGVSp=ENSP00000468424.1:p.Ala390Ser,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1299,CDS_position=1168,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749387380,VARIANT_CLASS=SNV,Protein_position=390,Codons=Gca/Tca,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1168G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1300	1300	0.0	.	.	AC_Male=1;AF_NFE=9.06208e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-28;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09954e-06;Hom=0;AF_POPMAX=9.06208e-06;AN_POPMAX=110350;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48783e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.29412e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.41699e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.23),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000468424.1:p.Ala390Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=11/13,cDNA_position=1300,CDS_position=1169,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=390,Codons=gCa/gTa,MINIMISED=1,HGVSc=ENST00000592782.1:c.1169C>T
CDS|ENST00000592782	VCF	missense_variant	1305	1305	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97631e-198;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63556e-05;Hom=0;AF_POPMAX=1.30881e-04;AN_POPMAX=30562;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.49365e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55398e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=170;AF_Female=1.80727e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=1.30881e-04;AS_RF=9.08567e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=4;POPMAX=SAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:3.362e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0002704,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.643),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/R,HGVSp=ENSP00000468424.1:p.Gly392Arg,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1305,CDS_position=1174,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs779143534&COSM1217528,VARIANT_CLASS=SNV,Protein_position=392,Codons=Gga/Aga,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000592782.1:c.1174G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1308	1308	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-80;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08320e-06;Hom=0;AF_POPMAX=1.02333e-04;AN_POPMAX=9772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=7.35294e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.02333e-04;DP_MEDIAN=34;AF_Female=9.02266e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.21409e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.375e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.51e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000468424.1:p.Glu393Lys,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1308,CDS_position=1177,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs748344051,VARIANT_CLASS=SNV,Protein_position=393,Codons=Gag/Aag,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.1177G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1336	1336	0.0	.	.	AC_Male=1;AF_NFE=1.79724e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|0|0|0|0|0|2|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-33;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22190e-05;Hom=0;AF_POPMAX=5.80316e-05;AN_POPMAX=17232;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43572e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.33761e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=1.80125e-05;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20100e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80316e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.256e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.761),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/M,HGVSp=ENSP00000468424.1:p.Thr402Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1336,CDS_position=1205,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs773052955&COSM1679874,VARIANT_CLASS=SNV,Protein_position=402,Codons=aCg/aTg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1205C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1350	1350	0.0	.	.	AC_Male=1;AF_NFE=8.95560e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06164e-06;Hom=0;AF_POPMAX=8.95560e-06;AN_POPMAX=111662;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41444e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.94824e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=483;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40352e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.241e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.5e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.021),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000468424.1:p.Ile407Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=G:0,cDNA_position=1350,CDS_position=1219,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs770912575,VARIANT_CLASS=SNV,Protein_position=407,Codons=Atc/Gtc,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.1219A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1366	1366	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-304;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.47876e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=259;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.21770e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.56),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/N,HGVSp=ENSP00000468424.1:p.Thr412Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1366,CDS_position=1235,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs776660504,VARIANT_CLASS=SNV,Protein_position=412,Codons=aCc/aAc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.1235C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1375	1375	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-112;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.12903e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=62;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.83306e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=S/N,HGVSp=ENSP00000468424.1:p.Ser415Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/13,cDNA_position=1375,CDS_position=1244,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=415,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000592782.1:c.1244G>A
CDS|ENST00000592782	VCF	missense_variant	1402	1402	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06058e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41235e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.93082e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=318;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36790e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.236e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.092),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000468424.1:p.Asn424Ser,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=G:0,cDNA_position=1402,CDS_position=1271,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs775334053,VARIANT_CLASS=SNV,Protein_position=424,Codons=aAc/aGc,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.1271A>G,ExAC_Adj_MAF=G:8.637e-05
CDS|ENST00000592782	VCF	missense_variant	1404	1404	0.0	.	.	AC_Male=0;AF_NFE=4.47571e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|4|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-115;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84248e-05;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|3|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=9;AB_MEDIAN=4.67391e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=91;AF_Female=6.28603e-05;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=1;AF_SAS=0.00000e+00;AS_RF=9.08698e-01;Hom_AMR=0;AC_EAS=1;AC_Female=7;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.65450e-05;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.18),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.647e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.072),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=V/I,HGVSp=ENSP00000468424.1:p.Val425Ile,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1404,CDS_position=1273,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767839828,VARIANT_CLASS=SNV,Protein_position=425,Codons=Gtt/Att,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592782.1:c.1273G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1436	1436	0.0	.	.	AC_Male=11;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|8|4|11|4|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-90;AF_OTH=1.45826e-03;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=8;Hom_Male=0;AC=29;Hom_NFE=0;AF=1.17774e-04;Hom=1;AF_POPMAX=5.95557e-04;AN_POPMAX=33582;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=1;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|2|2|1|5|3|1|0|1|0;AF_Male=8.15407e-05;AF_AFR=0.00000e+00;AC_raw=29;AB_MEDIAN=4.58333e-01;Hom_EAS=0;AC_AMR=20;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=1.61679e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|28;Hom_raw=1;AF_SAS=0.00000e+00;AS_RF=9.54732e-01;Hom_AMR=0;AC_EAS=0;AC_Female=18;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=20;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.17756e-04;Hom_Female=1;AF_AMR=5.95557e-04;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.17),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:0.0001483,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:7.492e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.074),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/I,HGVSp=ENSP00000468424.1:p.Met435Ile,STRAND=1,ExAC_SAS_MAF=T:0.001101,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=T:0,cDNA_position=1436,CDS_position=1305,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs750807200,VARIANT_CLASS=SNV,Protein_position=435,Codons=atG/atT,MINIMISED=1,ExAC_AFR_MAF=T:1.483e-04,HGVSc=ENST00000592782.1:c.1305G>T,ExAC_Adj_MAF=T:0.001036
CDS|ENST00000592782	VCF	missense_variant	1440	1440	0.0	.	.	AC_Male=1;AF_NFE=8.95207e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06161e-06;Hom=0;AF_POPMAX=8.95207e-06;AN_POPMAX=111706;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41345e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.25597e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=293;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.498e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.977),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=D/N,HGVSp=ENSP00000468424.1:p.Asp437Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1440,CDS_position=1309,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs766935430,VARIANT_CLASS=SNV,Protein_position=437,Codons=Gac/Aac,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.1309G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1443	1443	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-104;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06187e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.88636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=88;AF_Female=8.98424e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.14239e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.699),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000468424.1:p.Ala438Thr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=11/13,ExAC_AMR_MAF=A:0,cDNA_position=1443,CDS_position=1312,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs755095071&COSM4067024,VARIANT_CLASS=SNV,Protein_position=438,Codons=Gcc/Acc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.1312G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1455	1455	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50468e-04;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06587e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.78711e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.99507e-06;GQ_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44500e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.972),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000468424.1:p.Ala442Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/13,cDNA_position=1455,CDS_position=1324,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=442,Codons=Gcc/Acc,MINIMISED=1,HGVSc=ENST00000592782.1:c.1324G>A
CDS|ENST00000592782	VCF	missense_variant	1483	1483	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-103;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06062e-06;Hom=0;AF_POPMAX=1.01523e-04;AN_POPMAX=9850;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.31818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.01523e-04;DP_MEDIAN=88;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50356e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.935),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000468424.1:p.Asn451Ser,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=12/13,cDNA_position=1483,CDS_position=1352,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=451,Codons=aAt/aGt,MINIMISED=1,HGVSc=ENST00000592782.1:c.1352A>G
CDS|ENST00000592782	VCF	missense_variant	1485	1485	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-151;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=108;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43418e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.927),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000468424.1:p.Ala452Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=12/13,cDNA_position=1485,CDS_position=1354,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=452,Codons=Gca/Aca,MINIMISED=1,HGVSc=ENST00000592782.1:c.1354G>A
CDS|ENST00000592782	VCF	missense_variant	1506	1506	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-121;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.56311e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.26486e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.45),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.016),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=K/E,HGVSp=ENSP00000468424.1:p.Lys459Glu,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=12/13,cDNA_position=1506,CDS_position=1375,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=459,Codons=Aaa/Gaa,MINIMISED=1,HGVSc=ENST00000592782.1:c.1375A>G
CDS|ENST00000592782	VCF	missense_variant	1510	1510	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-44;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.63636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.14571e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.24),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=T/N,HGVSp=ENSP00000468424.1:p.Thr460Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=12/13,ExAC_AMR_MAF=A:0,cDNA_position=1510,CDS_position=1379,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs772801108,VARIANT_CLASS=SNV,Protein_position=460,Codons=aCc/aAc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.1379C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	missense_variant	1515	1515	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-140;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=6.53509e-05;AN_POPMAX=15302;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41246e-06;AF_AFR=6.53509e-05;AC_raw=1;AB_MEDIAN=5.10638e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.98),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/M,HGVSp=ENSP00000468424.1:p.Leu462Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=A,IMPACT=MODERATE,EXON=12/13,ExAC_AMR_MAF=T:0,cDNA_position=1515,CDS_position=1384,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs141629884,VARIANT_CLASS=SNV,Protein_position=462,Codons=Ctg/Atg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.1384C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	missense_variant	1536	1536	0.0	.	.	AC_Male=10;AF_NFE=9.84622e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|2|7|4|0|1|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-84;AF_OTH=3.64564e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=18;Hom_NFE=0;AF=7.30917e-05;Hom=0;AF_POPMAX=1.48889e-04;AN_POPMAX=33582;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|1|1|1|1|1|0|1|1|0|1|1|1;AF_Male=7.41246e-05;AF_AFR=0.00000e+00;AC_raw=18;AB_MEDIAN=4.35440e-01;Hom_EAS=0;AC_AMR=5;AF_ASJ=0.00000e+00;DP_MEDIAN=80;AF_Female=7.18404e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|18;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44331e-01;Hom_AMR=0;AC_EAS=0;AC_Female=8;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=7.30899e-05;Hom_Female=0;AF_AMR=1.48889e-04;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.19),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:4.943e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:7.495e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000468424.1:p.Ile469Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=12/13,ExAC_AMR_MAF=G:0,cDNA_position=1536,CDS_position=1405,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774301899,VARIANT_CLASS=SNV,Protein_position=469,Codons=Ata/Gta,MINIMISED=1,ExAC_AFR_MAF=G:4.942e-05,HGVSc=ENST00000592782.1:c.1405A>G,ExAC_Adj_MAF=G:8.642e-05
CDS|ENST00000592782	VCF	missense_variant	1545	1545	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-262;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=1.01543e-04;AN_POPMAX=9848;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57547e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.01543e-04;DP_MEDIAN=212;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.98494e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.977),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000468424.1:p.Gly472Ser,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=12/13,cDNA_position=1545,CDS_position=1414,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=472,Codons=Ggc/Agc,MINIMISED=1,HGVSc=ENST00000592782.1:c.1414G>A
CDS|ENST00000592782	VCF	missense_variant	1587	1587	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-133;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06114e-06;Hom=0;AF_POPMAX=2.97796e-05;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41323e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.33333e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=90;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.15969e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.36),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.023),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=M/L,HGVSp=ENSP00000468424.1:p.Met486Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=12/13,cDNA_position=1587,CDS_position=1456,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=486,Codons=Atg/Ttg,MINIMISED=1,HGVSc=ENST00000592782.1:c.1456A>T
CDS|ENST00000592782	VCF	missense_variant	1591	1591	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-120;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06167e-06;Hom=0;AF_POPMAX=2.97796e-05;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41367e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.81481e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=108;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.53),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=G/A,HGVSp=ENSP00000468424.1:p.Gly487Ala,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=12/13,cDNA_position=1591,CDS_position=1460,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=487,Codons=gGg/gCg,MINIMISED=1,HGVSc=ENST00000592782.1:c.1460G>C
CDS|ENST00000592782	VCF	missense_variant	1594	1594	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-220;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06197e-06;Hom=0;AF_POPMAX=2.97796e-05;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.64417e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=163;AF_Female=8.98376e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50841e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.095),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000468424.1:p.Ala488Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=12/13,cDNA_position=1594,CDS_position=1463,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=488,Codons=gCa/gTa,MINIMISED=1,HGVSc=ENST00000592782.1:c.1463C>T
CDS|ENST00000592782	VCF	missense_variant	1597	1597	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-187;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06177e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.68807e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=109;AF_Female=8.98279e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.40367e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.12),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.248e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=G:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,EAS_MAF=G:0,EUR_MAF=G:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,GMAF=G:0.0002,Amino_acids=E/G,HGVSp=ENSP00000468424.1:p.Glu489Gly,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=12/13,ExAC_AMR_MAF=G:0,cDNA_position=1597,CDS_position=1466,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs578117787,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=489,AA_MAF=G:0.001,Codons=gAg/gGg,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592782.1:c.1466A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1599	1599	0.0	.	.	AC_Male=1;AF_NFE=1.79115e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-88;AF_OTH=1.82482e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21862e-05;Hom=0;AF_POPMAX=1.79115e-05;AN_POPMAX=111660;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|1|0;AF_Male=7.41444e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=62;AF_Female=1.79682e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.5),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.65e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.001e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.102),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=K/E,HGVSp=ENSP00000468424.1:p.Lys490Glu,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=12/13,ExAC_AMR_MAF=G:0,cDNA_position=1599,CDS_position=1468,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs766069961,VARIANT_CLASS=SNV,Protein_position=490,Codons=Aag/Gag,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.1468A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	missense_variant	1600	1600	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-127;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06220e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.41444e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.34091e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=88;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.05),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.152),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=missense_variant&splice_region_variant,Amino_acids=K/R,HGVSp=ENSP00000468424.1:p.Lys490Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=12/13,cDNA_position=1600,CDS_position=1469,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=490,Codons=aAg/aGg,MINIMISED=1,HGVSc=ENST00000592782.1:c.1469A>G
CDS|ENST00000592782	VCF	missense_variant	1608	1608	0.0	.	.	AC_Male=1;AF_NFE=1.79263e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.76188e-107;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14180e-06;Hom=0;AF_POPMAX=1.79263e-05;AN_POPMAX=111568;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AF_Male=7.42732e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.90799e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=9.00836e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96721e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.437),SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000468424.1:p.Leu493Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=13/13,ExAC_AMR_MAF=G:0,cDNA_position=1608,CDS_position=1477,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs765115917,VARIANT_CLASS=SNV,Protein_position=493,Codons=Ctg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.1477C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	dbSNP	sequence_variant	2	2	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1315458524;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3	3	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1377204025;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4	4	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1314785806;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	5	5	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs978102949;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	6	6	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs945693006;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	7	7	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1244515398;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	10	10	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1275873848;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	11	11	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs977760428;alleles=C%2CA%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	12	12	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1187681935;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	13	21	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1475796189;alleles=GCGGGCGAG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	22	22	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1203332605;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	23	23	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs958390136;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	24	24	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs935908348;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	25	25	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs989644169;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	26	26	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1272239949;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	27	27	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1233710343;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	28	28	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1357234262;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	35	36	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1384739106;alleles=-%2CGC
CDS|ENST00000592782	dbSNP	sequence_variant	36	37	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1286435224;alleles=GC%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	38	38	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1440079030;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	41	41	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs922110352;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	46	65	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1329778382;alleles=GCAGACCGGACGTCCGGCCA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	66	66	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs932193844;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	68	69	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1157673972;alleles=-%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	72	72	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1253992663;alleles=G%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	72	72	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1423229683;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	73	73	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1170852352;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	75	75	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1252014907;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	76	76	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs544970256;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	78	78	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1427374379;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	85	85	0.0	+	.	consequence_type=splice_region_variant;id=rs763044000;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	87	88	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs575731887;alleles=-%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	92	92	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1359045430;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	93	93	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs768711397;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	94	94	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs774371000;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	95	95	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs370358129;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	97	97	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1289607294;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	98	98	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1361532932;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	99	99	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs374273277;alleles=G%2CA%2CC%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	100	100	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1371562848;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	101	101	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs373569442;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	102	102	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1324422483;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	103	103	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs765574685;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	105	105	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs369298290;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	106	106	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs778268422;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	107	107	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1216248878;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	111	111	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1241375845;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	113	113	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs752016137;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	114	114	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs757362692;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	115	115	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs746125540;alleles=T%2CC%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	116	116	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1479843107;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	117	117	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1199265434;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	118	118	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs779782774;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	119	119	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs749106795;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	121	121	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs768521050;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	122	122	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1345027263;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	126	126	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs892415557;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	127	127	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs774460908;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	129	129	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs748067291;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	131	131	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1346180677;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	136	136	0.0	+	.	consequence_type=missense_variant;id=rs771527303;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	138	138	0.0	+	.	consequence_type=missense_variant;id=rs772761859;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	139	139	0.0	+	.	consequence_type=missense_variant;id=rs1317068708;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	141	141	0.0	+	.	consequence_type=missense_variant;id=rs983223652;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	142	142	0.0	+	.	consequence_type=missense_variant;id=rs760309598;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	144	144	0.0	+	.	consequence_type=missense_variant;id=rs564172691;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	145	145	0.0	+	.	consequence_type=missense_variant;id=rs1314954450;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	146	146	0.0	+	.	consequence_type=synonymous_variant;id=rs1009445042;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	147	147	0.0	+	.	consequence_type=missense_variant;id=rs267604914;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	149	149	0.0	+	.	consequence_type=synonymous_variant;id=rs776210749;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	150	150	0.0	+	.	consequence_type=missense_variant;id=rs1292079143;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	151	151	0.0	+	.	consequence_type=missense_variant;id=rs1022554088;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	152	152	0.0	+	.	consequence_type=synonymous_variant;id=rs763334167;alleles=A%2CC%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	153	153	0.0	+	.	consequence_type=missense_variant;id=rs907713546;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	154	154	0.0	+	.	consequence_type=missense_variant;id=rs764406772;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	155	155	0.0	+	.	consequence_type=synonymous_variant;id=rs1253429311;alleles=A%2CC%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	156	156	0.0	+	.	consequence_type=missense_variant;id=rs752105945;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	161	161	0.0	+	.	consequence_type=synonymous_variant;id=rs757761311;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	162	162	0.0	+	.	consequence_type=missense_variant;id=rs767553043;alleles=C%2CA%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	163	163	0.0	+	.	consequence_type=missense_variant;id=rs750513385;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	164	164	0.0	+	.	consequence_type=synonymous_variant;id=rs1007666082;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	165	180	0.0	+	.	consequence_type=frameshift_variant;id=rs1306813664;alleles=CCGGCACCTCCGCTGC%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	181	181	0.0	+	.	consequence_type=missense_variant;id=rs937347334;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	185	185	0.0	+	.	consequence_type=synonymous_variant;id=rs1229832497;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	187	187	0.0	+	.	consequence_type=missense_variant;id=rs1315229471;alleles=T%2CC%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	190	190	0.0	+	.	consequence_type=missense_variant;id=rs772952636;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	194	195	0.0	+	.	consequence_type=inframe_insertion;id=rs1219870401;alleles=-%2CGGGAAC
CDS|ENST00000592782	dbSNP	sequence_variant	201	201	0.0	+	.	consequence_type=missense_variant;id=rs746539074;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	202	202	0.0	+	.	consequence_type=missense_variant;id=rs1437942507;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	204	205	0.0	+	.	consequence_type=inframe_insertion;id=rs763191382;alleles=-%2CACGGCC
CDS|ENST00000592782	dbSNP	sequence_variant	207	207	0.0	+	.	consequence_type=missense_variant;id=rs770300796;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	208	208	0.0	+	.	consequence_type=missense_variant;id=rs1451260585;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	211	211	0.0	+	.	consequence_type=missense_variant;id=rs1362841019;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	212	212	0.0	+	.	consequence_type=missense_variant;id=rs776300314;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	213	213	0.0	+	.	consequence_type=missense_variant;id=rs1159616651;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	214	214	0.0	+	.	consequence_type=missense_variant;id=rs1185809906;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	218	218	0.0	+	.	consequence_type=missense_variant;id=rs759161485;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	220	220	0.0	+	.	consequence_type=missense_variant;id=rs764495116;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	222	222	0.0	+	.	consequence_type=missense_variant;id=rs774684452;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	225	225	0.0	+	.	consequence_type=missense_variant;id=rs976121906;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	229	229	0.0	+	.	consequence_type=missense_variant;id=rs895881728;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	230	230	0.0	+	.	consequence_type=missense_variant;id=rs762294220;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	233	233	0.0	+	.	consequence_type=synonymous_variant;id=rs768076232;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	242	242	0.0	+	.	consequence_type=synonymous_variant;id=rs1328029981;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	251	251	0.0	+	.	consequence_type=missense_variant;id=rs750844557;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	253	253	0.0	+	.	consequence_type=missense_variant;id=rs756247053;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	255	257	0.0	+	.	consequence_type=inframe_deletion;id=rs375981533;alleles=AAC%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	259	259	0.0	+	.	consequence_type=missense_variant;id=rs1271597368;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	260	260	0.0	+	.	consequence_type=splice_region_variant;id=rs143955814;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	265	265	0.0	+	.	consequence_type=missense_variant;id=rs752810524;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	267	267	0.0	+	.	consequence_type=missense_variant;id=rs758247752;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	268	268	0.0	+	.	consequence_type=missense_variant;id=rs1199096532;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	271	271	0.0	+	.	consequence_type=missense_variant;id=rs1286861992;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	272	272	0.0	+	.	consequence_type=synonymous_variant;id=rs777402320;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	273	273	0.0	+	.	consequence_type=missense_variant;id=rs1192808116;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	274	274	0.0	+	.	consequence_type=missense_variant;id=rs1212522731;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	279	279	0.0	+	.	consequence_type=missense_variant;id=rs140455291;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	280	280	0.0	+	.	consequence_type=missense_variant;id=rs757177482;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	292	292	0.0	+	.	consequence_type=missense_variant;id=rs780748535;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	295	295	0.0	+	.	consequence_type=missense_variant;id=rs774451911;alleles=A%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	307	307	0.0	+	.	consequence_type=missense_variant;id=rs1468231466;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	312	312	0.0	+	.	consequence_type=missense_variant;id=rs3087878;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	317	317	0.0	+	.	consequence_type=synonymous_variant;id=rs375158125;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	322	322	0.0	+	.	consequence_type=missense_variant;id=rs201559014;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	324	324	0.0	+	.	consequence_type=missense_variant;id=rs779784731;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	332	332	0.0	+	.	consequence_type=synonymous_variant;id=rs141656657;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	334	334	0.0	+	.	consequence_type=missense_variant;id=rs1399730029;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	335	335	0.0	+	.	consequence_type=synonymous_variant;id=rs1315823029;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	341	341	0.0	+	.	consequence_type=synonymous_variant;id=rs369434915;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	351	351	0.0	+	.	consequence_type=missense_variant;id=rs1405046109;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	352	352	0.0	+	.	consequence_type=missense_variant;id=rs1284414737;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	353	353	0.0	+	.	consequence_type=synonymous_variant;id=rs184508172;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	356	356	0.0	+	.	consequence_type=missense_variant;id=rs1231776580;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	360	360	0.0	+	.	consequence_type=missense_variant;id=rs1281614790;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	366	366	0.0	+	.	consequence_type=missense_variant;id=rs761306458;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	372	372	0.0	+	.	consequence_type=start_lost;id=rs767459577;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	376	376	0.0	+	.	consequence_type=missense_variant;id=rs367954716;alleles=A%2CC%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	380	380	0.0	+	.	consequence_type=synonymous_variant;id=rs200633656;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	383	383	0.0	+	.	consequence_type=missense_variant;id=rs1018863986;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	392	392	0.0	+	.	consequence_type=missense_variant;id=rs1051019368;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	398	398	0.0	+	.	consequence_type=missense_variant;id=rs779405921;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	404	404	0.0	+	.	consequence_type=synonymous_variant;id=rs1382805858;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	417	417	0.0	+	.	consequence_type=missense_variant;id=rs1463089836;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	418	418	0.0	+	.	consequence_type=missense_variant;id=rs1308984921;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	419	419	0.0	+	.	consequence_type=synonymous_variant;id=rs372318247;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	425	425	0.0	+	.	consequence_type=synonymous_variant;id=rs754577624;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	431	431	0.0	+	.	consequence_type=synonymous_variant;id=rs1391388443;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	433	433	0.0	+	.	consequence_type=missense_variant;id=rs778561485;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	435	435	0.0	+	.	consequence_type=missense_variant;id=rs747390700;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	439	439	0.0	+	.	consequence_type=missense_variant;id=rs1335366133;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	440	440	0.0	+	.	consequence_type=missense_variant;id=rs771371139;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	441	441	0.0	+	.	consequence_type=missense_variant;id=rs563736659;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	443	443	0.0	+	.	consequence_type=synonymous_variant;id=rs746348189;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	444	444	0.0	+	.	consequence_type=missense_variant;id=rs1294041634;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	445	445	0.0	+	.	consequence_type=missense_variant;id=rs1416691571;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	447	447	0.0	+	.	consequence_type=missense_variant;id=rs868718436;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	449	449	0.0	+	.	consequence_type=synonymous_variant;id=rs1229714849;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	456	456	0.0	+	.	consequence_type=missense_variant;id=rs1348860194;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	457	457	0.0	+	.	consequence_type=missense_variant;id=rs770043528;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	463	463	0.0	+	.	consequence_type=missense_variant;id=rs775419569;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	464	464	0.0	+	.	consequence_type=synonymous_variant;id=rs972147914;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	465	465	0.0	+	.	consequence_type=missense_variant;id=rs1297768336;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	466	466	0.0	+	.	consequence_type=missense_variant;id=rs1443418786;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	467	467	0.0	+	.	consequence_type=synonymous_variant;id=rs1338651806;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	468	468	0.0	+	.	consequence_type=missense_variant;id=rs1196722115;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	470	470	0.0	+	.	consequence_type=synonymous_variant;id=rs1244710451;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	475	475	0.0	+	.	consequence_type=missense_variant;id=rs377156745;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	477	477	0.0	+	.	consequence_type=missense_variant;id=rs1182546534;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	484	484	0.0	+	.	consequence_type=missense_variant;id=rs1391284036;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	488	488	0.0	+	.	consequence_type=synonymous_variant;id=rs1253657974;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	496	496	0.0	+	.	consequence_type=missense_variant;id=rs764230766;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	497	497	0.0	+	.	consequence_type=synonymous_variant;id=rs1170526700;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	503	503	0.0	+	.	consequence_type=synonymous_variant;id=rs774578466;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	504	504	0.0	+	.	consequence_type=missense_variant;id=rs761622308;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	509	509	0.0	+	.	consequence_type=synonymous_variant;id=rs767261647;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	511	511	0.0	+	.	consequence_type=missense_variant;id=rs144433221;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	518	518	0.0	+	.	consequence_type=splice_region_variant;id=rs199678185;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	523	523	0.0	+	.	consequence_type=missense_variant;id=rs1216003679;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	530	530	0.0	+	.	consequence_type=synonymous_variant;id=rs760391896;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	533	533	0.0	+	.	consequence_type=synonymous_variant;id=rs766241230;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	534	534	0.0	+	.	consequence_type=missense_variant;id=rs753759265;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	539	539	0.0	+	.	consequence_type=synonymous_variant;id=rs1269052802;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	542	542	0.0	+	.	consequence_type=synonymous_variant;id=rs147841016;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	543	543	0.0	+	.	consequence_type=missense_variant;id=rs752448187;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	548	548	0.0	+	.	consequence_type=synonymous_variant;id=rs1250252141;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	549	549	0.0	+	.	consequence_type=missense_variant;id=rs758111913;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	550	550	0.0	+	.	consequence_type=missense_variant;id=rs1421268751;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	552	552	0.0	+	.	consequence_type=missense_variant;id=rs201386803;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	554	554	0.0	+	.	consequence_type=synonymous_variant;id=rs535242567;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	555	555	0.0	+	.	consequence_type=missense_variant;id=rs986408291;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	557	557	0.0	+	.	consequence_type=synonymous_variant;id=rs1418173661;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	568	568	0.0	+	.	consequence_type=missense_variant;id=rs955288678;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	569	569	0.0	+	.	consequence_type=synonymous_variant;id=rs1456376961;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	570	570	0.0	+	.	consequence_type=missense_variant;id=rs1161073719;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	573	573	0.0	+	.	consequence_type=missense_variant;id=rs1305018160;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	575	575	0.0	+	.	consequence_type=synonymous_variant;id=rs910463482;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	576	576	0.0	+	.	consequence_type=missense_variant;id=rs1366323829;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	591	591	0.0	+	.	consequence_type=stop_gained;id=rs1435626124;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	594	594	0.0	+	.	consequence_type=missense_variant;id=rs1291739811;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	602	602	0.0	+	.	consequence_type=synonymous_variant;id=rs559376009;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	612	612	0.0	+	.	consequence_type=synonymous_variant;id=rs1199425750;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	618	618	0.0	+	.	consequence_type=synonymous_variant;id=rs1132898;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	620	620	0.0	+	.	consequence_type=synonymous_variant;id=rs1306112590;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	623	623	0.0	+	.	consequence_type=synonymous_variant;id=rs749766632;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	624	624	0.0	+	.	consequence_type=missense_variant;id=rs149737135;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	627	627	0.0	+	.	consequence_type=missense_variant;id=rs778948844;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	628	628	0.0	+	.	consequence_type=missense_variant;id=rs748432196;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	629	629	0.0	+	.	consequence_type=synonymous_variant;id=rs1221407945;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	630	630	0.0	+	.	consequence_type=missense_variant;id=rs1269207571;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	632	632	0.0	+	.	consequence_type=synonymous_variant;id=rs772281237;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	633	633	0.0	+	.	consequence_type=missense_variant;id=rs773364852;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	645	645	0.0	+	.	consequence_type=missense_variant;id=rs1377176181;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	653	653	0.0	+	.	consequence_type=missense_variant;id=rs770678984;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	659	659	0.0	+	.	consequence_type=missense_variant;id=rs927057705;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	671	671	0.0	+	.	consequence_type=synonymous_variant;id=rs151247418;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	686	686	0.0	+	.	consequence_type=synonymous_variant;id=rs776474941;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	689	689	0.0	+	.	consequence_type=synonymous_variant;id=rs1410437263;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	690	690	0.0	+	.	consequence_type=missense_variant;id=rs1283407561;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	701	701	0.0	+	.	consequence_type=synonymous_variant;id=rs759459614;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	710	710	0.0	+	.	consequence_type=synonymous_variant;id=rs372926712;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	712	712	0.0	+	.	consequence_type=missense_variant;id=rs775510228;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	713	713	0.0	+	.	consequence_type=synonymous_variant;id=rs146345914;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	714	714	0.0	+	.	consequence_type=missense_variant;id=rs1339503876;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	715	715	0.0	+	.	consequence_type=missense_variant;id=rs1445433341;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	716	716	0.0	+	.	consequence_type=missense_variant;id=rs866488889;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	717	717	0.0	+	.	consequence_type=missense_variant;id=rs1311826897;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	723	723	0.0	+	.	consequence_type=synonymous_variant;id=rs1259891285;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	735	735	0.0	+	.	consequence_type=missense_variant;id=rs764148755;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	736	736	0.0	+	.	consequence_type=missense_variant;id=rs150418753;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	743	743	0.0	+	.	consequence_type=synonymous_variant;id=rs757227703;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	744	744	0.0	+	.	consequence_type=missense_variant;id=rs781499966;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	749	749	0.0	+	.	consequence_type=missense_variant;id=rs746041079;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	750	750	0.0	+	.	consequence_type=missense_variant;id=rs756018179;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	752	752	0.0	+	.	consequence_type=synonymous_variant;id=rs369385342;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	754	754	0.0	+	.	consequence_type=missense_variant;id=rs779975972;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	770	770	0.0	+	.	consequence_type=synonymous_variant;id=rs768715452;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	780	780	0.0	+	.	consequence_type=missense_variant;id=rs774095582;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	782	782	0.0	+	.	consequence_type=synonymous_variant;id=rs199671891;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	788	788	0.0	+	.	consequence_type=synonymous_variant;id=rs112989351;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	789	789	0.0	+	.	consequence_type=missense_variant;id=rs1407256029;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	790	790	0.0	+	.	consequence_type=missense_variant;id=rs771441667;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	791	791	0.0	+	.	consequence_type=synonymous_variant;id=rs1330823537;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	794	794	0.0	+	.	consequence_type=synonymous_variant;id=rs1259991653;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	809	809	0.0	+	.	consequence_type=missense_variant;id=rs1303544092;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	810	810	0.0	+	.	consequence_type=missense_variant;id=rs919282095;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	812	812	0.0	+	.	consequence_type=synonymous_variant;id=rs772957252;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	818	818	0.0	+	.	consequence_type=missense_variant;id=rs375089291;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	821	821	0.0	+	.	consequence_type=synonymous_variant;id=rs770200317;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	832	832	0.0	+	.	consequence_type=missense_variant;id=rs775829411;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	838	838	0.0	+	.	consequence_type=missense_variant;id=rs763238851;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	839	839	0.0	+	.	consequence_type=synonymous_variant;id=rs1490869430;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	843	843	0.0	+	.	consequence_type=missense_variant;id=rs1342497115;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	844	844	0.0	+	.	consequence_type=missense_variant;id=rs764674925;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	845	845	0.0	+	.	consequence_type=splice_region_variant;id=rs752735481;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	853	853	0.0	+	.	consequence_type=missense_variant;id=rs758261924;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	855	855	0.0	+	.	consequence_type=missense_variant;id=rs777621617;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	869	869	0.0	+	.	consequence_type=synonymous_variant;id=rs1336872685;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	876	876	0.0	+	.	consequence_type=missense_variant;id=rs1331451303;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	891	891	0.0	+	.	consequence_type=synonymous_variant;id=rs1006739593;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	893	893	0.0	+	.	consequence_type=synonymous_variant;id=rs1264834130;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	895	895	0.0	+	.	consequence_type=missense_variant;id=rs746537411;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	899	899	0.0	+	.	consequence_type=synonymous_variant;id=rs770379933;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	905	905	0.0	+	.	consequence_type=synonymous_variant;id=rs780855060;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	911	911	0.0	+	.	consequence_type=synonymous_variant;id=rs1163522330;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	912	912	0.0	+	.	consequence_type=missense_variant;id=rs1429798567;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	929	929	0.0	+	.	consequence_type=synonymous_variant;id=rs146578323;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	935	935	0.0	+	.	consequence_type=synonymous_variant;id=rs970102977;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	950	950	0.0	+	.	consequence_type=synonymous_variant;id=rs201216212;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	951	951	0.0	+	.	consequence_type=missense_variant;id=rs1422769066;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	954	954	0.0	+	.	consequence_type=missense_variant;id=rs367724198;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	957	957	0.0	+	.	consequence_type=missense_variant;id=rs371122860;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	962	962	0.0	+	.	consequence_type=synonymous_variant;id=rs766086965;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	967	967	0.0	+	.	consequence_type=missense_variant;id=rs1196654054;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	969	969	0.0	+	.	consequence_type=missense_variant;id=rs772467109;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	978	978	0.0	+	.	consequence_type=missense_variant;id=rs1302511754;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	980	980	0.0	+	.	consequence_type=synonymous_variant;id=rs773804544;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	982	982	0.0	+	.	consequence_type=missense_variant;id=rs766531390;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	983	983	0.0	+	.	consequence_type=synonymous_variant;id=rs777042262;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	989	989	0.0	+	.	consequence_type=synonymous_variant;id=rs1266795902;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	990	990	0.0	+	.	consequence_type=missense_variant;id=rs759663986;alleles=C%2CA%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	992	992	0.0	+	.	consequence_type=synonymous_variant;id=rs765144876;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	995	995	0.0	+	.	consequence_type=synonymous_variant;id=rs1284923476;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1001	1001	0.0	+	.	consequence_type=synonymous_variant;id=rs2239922;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1002	1002	0.0	+	.	consequence_type=missense_variant;id=rs376218058;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1006	1006	0.0	+	.	consequence_type=missense_variant;id=rs764042790;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1010	1010	0.0	+	.	consequence_type=synonymous_variant;id=rs1486522613;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1027	1027	0.0	+	.	consequence_type=missense_variant;id=rs1204184516;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1041	1041	0.0	+	.	consequence_type=missense_variant;id=rs1441741328;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1047	1047	0.0	+	.	consequence_type=synonymous_variant;id=rs2239923;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1049	1049	0.0	+	.	consequence_type=synonymous_variant;id=rs985161494;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1052	1052	0.0	+	.	consequence_type=synonymous_variant;id=rs1379717035;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1058	1058	0.0	+	.	consequence_type=synonymous_variant;id=rs779600514;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1064	1064	0.0	+	.	consequence_type=synonymous_variant;id=rs1166748067;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1073	1073	0.0	+	.	consequence_type=synonymous_variant;id=rs1350394216;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1080	1080	0.0	+	.	consequence_type=missense_variant;id=rs1326078809;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1084	1084	0.0	+	.	consequence_type=missense_variant;id=rs1435733070;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1091	1091	0.0	+	.	consequence_type=missense_variant;id=rs1244829195;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1097	1097	0.0	+	.	consequence_type=synonymous_variant;id=rs772701064;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1098	1098	0.0	+	.	consequence_type=missense_variant;id=rs760110087;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1100	1100	0.0	+	.	consequence_type=synonymous_variant;id=rs1489341607;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1102	1102	0.0	+	.	consequence_type=missense_variant;id=rs1291541781;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1106	1106	0.0	+	.	consequence_type=synonymous_variant;id=rs1296557184;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1109	1109	0.0	+	.	consequence_type=synonymous_variant;id=rs1378878097;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1113	1113	0.0	+	.	consequence_type=missense_variant;id=rs1447003290;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1114	1114	0.0	+	.	consequence_type=missense_variant;id=rs1384334634;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1115	1115	0.0	+	.	consequence_type=synonymous_variant;id=rs748936607;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1117	1117	0.0	+	.	consequence_type=missense_variant;id=rs1193969791;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1119	1119	0.0	+	.	consequence_type=missense_variant;id=rs1373930583;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1125	1125	0.0	+	.	consequence_type=missense_variant;id=rs767459640;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1126	1126	0.0	+	.	consequence_type=missense_variant;id=rs750330678;alleles=C%2CA%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1127	1127	0.0	+	.	consequence_type=splice_region_variant;id=rs913514091;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1128	1128	0.0	+	.	consequence_type=missense_variant;id=rs1271946369;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1134	1134	0.0	+	.	consequence_type=missense_variant;id=rs1213935690;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1135	1135	0.0	+	.	consequence_type=missense_variant;id=rs375623297;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1136	1136	0.0	+	.	consequence_type=synonymous_variant;id=rs1258804913;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1137	1137	0.0	+	.	consequence_type=missense_variant;id=rs760138330;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1138	1138	0.0	+	.	consequence_type=missense_variant;id=rs1336327252;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1145	1145	0.0	+	.	consequence_type=synonymous_variant;id=rs1397891517;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1146	1146	0.0	+	.	consequence_type=stop_gained;id=rs1415777939;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1152	1152	0.0	+	.	consequence_type=missense_variant;id=rs554809034;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1160	1160	0.0	+	.	consequence_type=synonymous_variant;id=rs1438572701;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1165	1165	0.0	+	.	consequence_type=missense_variant;id=rs3194194;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1170	1170	0.0	+	.	consequence_type=missense_variant;id=rs1358012081;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1172	1172	0.0	+	.	consequence_type=synonymous_variant;id=rs1445179731;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1173	1173	0.0	+	.	consequence_type=missense_variant;id=rs753488937;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1178	1178	0.0	+	.	consequence_type=synonymous_variant;id=rs1342923786;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1179	1179	0.0	+	.	consequence_type=missense_variant;id=rs754671896;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1185	1185	0.0	+	.	consequence_type=missense_variant;id=rs778639871;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1193	1193	0.0	+	.	consequence_type=synonymous_variant;id=rs751985902;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1195	1195	0.0	+	.	consequence_type=missense_variant;id=rs757647993;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1196	1196	0.0	+	.	consequence_type=synonymous_variant;id=rs781580851;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1202	1202	0.0	+	.	consequence_type=missense_variant;id=rs1442131409;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1212	1212	0.0	+	.	consequence_type=missense_variant;id=rs1396950068;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1219	1219	0.0	+	.	consequence_type=missense_variant;id=rs1208099201;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1220	1220	0.0	+	.	consequence_type=synonymous_variant;id=rs746356993;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1221	1221	0.0	+	.	consequence_type=missense_variant;id=rs1352058986;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1223	1223	0.0	+	.	consequence_type=synonymous_variant;id=rs769815313;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1224	1224	0.0	+	.	consequence_type=missense_variant;id=rs148483868;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1225	1225	0.0	+	.	consequence_type=missense_variant;id=rs1192890144;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1226	1226	0.0	+	.	consequence_type=synonymous_variant;id=rs924982378;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1241	1241	0.0	+	.	consequence_type=synonymous_variant;id=rs1364693881;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1245	1245	0.0	+	.	consequence_type=missense_variant;id=rs943116623;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1260	1260	0.0	+	.	consequence_type=missense_variant;id=rs1478893273;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1262	1262	0.0	+	.	consequence_type=synonymous_variant;id=rs749581366;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1265	1265	0.0	+	.	consequence_type=synonymous_variant;id=rs1424024037;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1272	1272	0.0	+	.	consequence_type=missense_variant;id=rs1412459058;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1277	1277	0.0	+	.	consequence_type=synonymous_variant;id=rs1038857011;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1278	1278	0.0	+	.	consequence_type=missense_variant;id=rs1360643122;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1284	1284	0.0	+	.	consequence_type=missense_variant;id=rs1401094663;alleles=T%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1286	1286	0.0	+	.	consequence_type=synonymous_variant;id=rs768875089;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1289	1289	0.0	+	.	consequence_type=synonymous_variant;id=rs901665795;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1290	1290	0.0	+	.	consequence_type=missense_variant;id=rs1324984572;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1292	1292	0.0	+	.	consequence_type=synonymous_variant;id=rs774502405;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1295	1295	0.0	+	.	consequence_type=missense_variant;id=rs1275875591;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1297	1297	0.0	+	.	consequence_type=missense_variant;id=rs1259100523;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1298	1298	0.0	+	.	consequence_type=splice_region_variant;id=rs142226258;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1299	1299	0.0	+	.	consequence_type=missense_variant;id=rs749387380;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1300	1300	0.0	+	.	consequence_type=missense_variant;id=rs1288820933;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1304	1304	0.0	+	.	consequence_type=synonymous_variant;id=rs369014766;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1305	1305	0.0	+	.	consequence_type=missense_variant;id=rs779143534;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1308	1308	0.0	+	.	consequence_type=missense_variant;id=rs748344051;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1309	1309	0.0	+	.	consequence_type=missense_variant;id=rs983756350;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1316	1316	0.0	+	.	consequence_type=synonymous_variant;id=rs771817702;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1336	1336	0.0	+	.	consequence_type=missense_variant;id=rs773052955;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1337	1337	0.0	+	.	consequence_type=synonymous_variant;id=rs746713731;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1350	1350	0.0	+	.	consequence_type=missense_variant;id=rs770912575;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1358	1358	0.0	+	.	consequence_type=synonymous_variant;id=rs1164368260;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1366	1366	0.0	+	.	consequence_type=missense_variant;id=rs776660504;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1367	1367	0.0	+	.	consequence_type=synonymous_variant;id=rs759148893;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1375	1375	0.0	+	.	consequence_type=missense_variant;id=rs1333869222;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1376	1376	0.0	+	.	consequence_type=missense_variant;id=rs1186266047;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1379	1379	0.0	+	.	consequence_type=synonymous_variant;id=rs773592883;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1394	1394	0.0	+	.	consequence_type=synonymous_variant;id=rs1180139152;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1400	1400	0.0	+	.	consequence_type=synonymous_variant;id=rs764809965;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1402	1402	0.0	+	.	consequence_type=missense_variant;id=rs775334053;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1403	1403	0.0	+	.	consequence_type=synonymous_variant;id=rs143838999;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1404	1404	0.0	+	.	consequence_type=missense_variant;id=rs767839828;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1415	1415	0.0	+	.	consequence_type=missense_variant;id=rs1462397852;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1436	1436	0.0	+	.	consequence_type=missense_variant;id=rs750807200;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1439	1439	0.0	+	.	consequence_type=synonymous_variant;id=rs766390878;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1440	1440	0.0	+	.	consequence_type=missense_variant;id=rs766935430;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1442	1442	0.0	+	.	consequence_type=synonymous_variant;id=rs754018187;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1443	1443	0.0	+	.	consequence_type=missense_variant;id=rs755095071;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1446	1446	0.0	+	.	consequence_type=missense_variant;id=rs1241960333;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1454	1454	0.0	+	.	consequence_type=synonymous_variant;id=rs1057442373;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1455	1455	0.0	+	.	consequence_type=missense_variant;id=rs867687573;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1457	1457	0.0	+	.	consequence_type=synonymous_variant;id=rs778948819;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1473	1473	0.0	+	.	consequence_type=missense_variant;id=rs1802201;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1481	1481	0.0	+	.	consequence_type=missense_variant;id=rs908761902;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1483	1483	0.0	+	.	consequence_type=missense_variant;id=rs1350193710;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1485	1485	0.0	+	.	consequence_type=missense_variant;id=rs1460724762;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1486	1486	0.0	+	.	consequence_type=missense_variant;id=rs1279886973;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1493	1493	0.0	+	.	consequence_type=synonymous_variant;id=rs771722999;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1497	1497	0.0	+	.	consequence_type=missense_variant;id=rs1276441766;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1506	1506	0.0	+	.	consequence_type=missense_variant;id=rs1401993695;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1510	1510	0.0	+	.	consequence_type=missense_variant;id=rs772801108;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1511	1511	0.0	+	.	consequence_type=synonymous_variant;id=rs376284001;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1514	1514	0.0	+	.	consequence_type=synonymous_variant;id=rs556448466;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1515	1515	0.0	+	.	consequence_type=missense_variant;id=rs141629884;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1517	1517	0.0	+	.	consequence_type=synonymous_variant;id=rs372878120;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1526	1526	0.0	+	.	consequence_type=synonymous_variant;id=rs763355938;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1535	1535	0.0	+	.	consequence_type=synonymous_variant;id=rs369290804;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1536	1536	0.0	+	.	consequence_type=missense_variant;id=rs774301899;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1538	1538	0.0	+	.	consequence_type=frameshift_variant;id=rs1459236506;alleles=A%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1544	1544	0.0	+	.	consequence_type=synonymous_variant;id=rs1199543349;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1545	1545	0.0	+	.	consequence_type=missense_variant;id=rs1232327561;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1567	1567	0.0	+	.	consequence_type=missense_variant;id=rs1426104773;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1571	1571	0.0	+	.	consequence_type=synonymous_variant;id=rs373214072;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1574	1574	0.0	+	.	consequence_type=missense_variant;id=rs867051835;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1576	1576	0.0	+	.	consequence_type=missense_variant;id=rs898816298;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1580	1580	0.0	+	.	consequence_type=synonymous_variant;id=rs767877724;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1583	1583	0.0	+	.	consequence_type=synonymous_variant;id=rs200139594;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1587	1587	0.0	+	.	consequence_type=missense_variant;id=rs1474867123;alleles=A%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1591	1591	0.0	+	.	consequence_type=missense_variant;id=rs1162489791;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1594	1594	0.0	+	.	consequence_type=missense_variant;id=rs1425544391;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1597	1597	0.0	+	.	consequence_type=missense_variant;id=rs578117787;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1598	1598	0.0	+	.	consequence_type=synonymous_variant;id=rs1327777743;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1599	1599	0.0	+	.	consequence_type=missense_variant;id=rs766069961;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1600	1600	0.0	+	.	consequence_type=missense_variant;id=rs1449583852;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1608	1608	0.0	+	.	consequence_type=missense_variant;id=rs765115917;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1613	1613	0.0	+	.	consequence_type=synonymous_variant;id=rs752598763;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1614	1614	0.0	+	.	consequence_type=synonymous_variant;id=rs1330209973;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1616	1616	0.0	+	.	consequence_type=synonymous_variant;id=rs1465973808;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1621	1621	0.0	+	.	consequence_type=stop_lost;id=rs1421300928;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1624	1624	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1288068012;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1628	1628	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs747853709;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1630	1630	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1192178645;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1632	1633	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs763336808;alleles=-%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1634	1634	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1191436418;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1636	1636	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1393899624;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1637	1637	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs370761943;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1640	1640	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs756865994;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1643	1643	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1053733;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1646	1646	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1462863066;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1652	1652	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1401838250;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1659	1659	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749639976;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1663	1663	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs769028747;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1664	1664	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs371753337;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1679	1680	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1275487350;alleles=-%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1688	1688	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs369051195;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1691	1691	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1250182993;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1692	1692	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs374157641;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1698	1698	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs565164528;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1699	1699	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1037729069;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1710	1710	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141202848;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1711	1711	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541333000;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1713	1713	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs559236400;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1718	1718	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs981524641;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1723	1723	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1053739;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1724	1724	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1321337667;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1732	1732	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1171204481;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1737	1737	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1391338066;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1744	1744	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1165345478;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1746	1746	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs934409916;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1747	1747	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1054232876;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1749	1749	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178276522;alleles=T%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1753	1753	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1470631130;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1759	1759	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs960277341;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1760	1760	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs914389525;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1762	1762	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs771408813;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1765	1765	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs547873231;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1766	1766	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs563091154;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1772	1772	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs530405653;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1774	1774	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs551792359;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1785	1785	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs979139564;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1786	1786	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs891044536;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1788	1788	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1008191100;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1791	1791	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs114271764;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1792	1792	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1334496147;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1800	1800	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs964751422;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1801	1801	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897217919;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1805	1805	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs143311253;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1814	1814	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs923189525;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1815	1815	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs148324496;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1816	1816	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1401550841;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1818	1818	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs548069555;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1819	1819	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs566098238;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1823	1823	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1189649614;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1833	1833	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs959532407;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1834	1834	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1251272836;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1855	1855	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1462186783;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1856	1856	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1012864617;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1859	1859	0.0	+	.	consequence_type=splice_region_variant;id=rs1269977841;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1862	1862	0.0	+	.	consequence_type=splice_donor_variant;id=rs1202296343;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1863	1863	0.0	+	.	consequence_type=splice_region_variant;id=rs933216623;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1866	1866	0.0	+	.	consequence_type=splice_region_variant;id=rs1025193535;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1867	1867	0.0	+	.	consequence_type=splice_region_variant;id=rs971403946;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1879	1879	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs981101330;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1902	1902	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs369699233;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1909	1909	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1218212438;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1916	1916	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs942121531;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1926	1926	0.0	+	.	consequence_type=splice_region_variant;id=rs1187332688;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1929	1929	0.0	+	.	consequence_type=splice_donor_variant;id=rs1421671608;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1941	1943	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1398111547;alleles=AGT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1943	1944	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1037801267;alleles=TA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1946	1946	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1414106419;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1948	1948	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1430514004;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1949	1949	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs989895551;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1951	1955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1001942416;alleles=TATAT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1955	1956	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1010428709;alleles=-%2CTA
CDS|ENST00000592782	dbSNP	sequence_variant	1959	1959	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1209063133;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1965	1965	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs932467552;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1971	1971	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224841958;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1974	1975	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1429876784;alleles=-%2CTAAATA
CDS|ENST00000592782	dbSNP	sequence_variant	1981	1984	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1264823314;alleles=TCTT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1998	1998	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1317026015;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2012	2012	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1020440494;alleles=G%2CC%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2018	2018	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs17684744;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2035	2035	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs16939858;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2036	2037	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1407087325;alleles=AG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2052	2052	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1338891400;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2060	2060	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs796506744;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2061	2061	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs769885556;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2067	2067	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1423280480;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2073	2073	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1036938272;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2074	2074	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1171753731;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2078	2078	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1032510694;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2080	2080	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897144744;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2081	2081	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1359202111;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2082	2082	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs995508376;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2083	2083	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1048457718;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2084	2084	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244625323;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2090	2090	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs576637742;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2100	2100	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1196289397;alleles=T%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2106	2106	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs537427196;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2114	2114	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs895230067;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2116	2116	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs558645892;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2121	2121	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1012378907;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2127	2127	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1225957412;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2138	2139	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1261580556;alleles=AG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2143	2143	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs970947658;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2147	2147	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs577172913;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2153	2153	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1231594463;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2173	2173	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs757917677;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2184	2184	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1319821569;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2194	2194	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs775653407;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2201	2201	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1216711171;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2202	2202	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1031296585;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2208	2208	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955683670;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2216	2216	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1444766255;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2224	2224	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1400102884;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2226	2226	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1299100514;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2238	2238	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs973220799;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2241	2241	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs989821734;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2243	2243	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1348665604;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2247	2247	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs540927831;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2257	2284	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244092003;alleles=CTGGGGCTGACCCTGGGCAGGGACTTTC%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2285	2285	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs953948699;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2292	2292	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs559716890;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2294	2294	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438688265;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2298	2298	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1251023194;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2305	2305	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178702703;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2307	2307	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs574557884;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2309	2309	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs943909863;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2310	2310	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs972624417;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2323	2323	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs918540028;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2328	2328	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs376815066;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2329	2329	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1161070547;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2330	2330	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1238339324;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2337	2337	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1335370299;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2346	2346	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs724329;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2349	2352	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1343049988;alleles=ATTG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2360	2360	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1452671782;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2366	2366	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1365847420;alleles=T%2CA%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2377	2377	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141446378;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2380	2380	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1366968827;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2384	2384	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1000329032;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2389	2389	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs530491484;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2394	2394	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1364043446;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2397	2397	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs895200885;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2399	2399	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1160791533;alleles=C%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2400	2400	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs900289262;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2402	2402	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1407230545;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2413	2413	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200135795;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2416	2416	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1490819689;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2420	2420	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178689600;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2438	2438	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs995920796;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2442	2442	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1367298964;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2445	2445	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs948121222;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2446	2446	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1349991909;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2447	2447	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1430002785;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2451	2451	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1241377536;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2459	2459	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs766348222;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2462	2462	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283035619;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2467	2467	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906689685;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2469	2469	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs180906761;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2474	2474	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1381193691;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2475	2475	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs954372227;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2477	2477	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1290282779;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2500	2500	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs28421762;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2501	2501	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1376926156;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2505	2505	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs894064577;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2517	2517	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1176852360;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2527	2527	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1011223354;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2529	2529	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1292507701;alleles=G%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2534	2534	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1192761554;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2546	2546	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs963254927;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2558	2558	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446511726;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2560	2560	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs528096327;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2561	2561	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1207185525;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2565	2565	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1482380396;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2568	2568	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs927144783;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2578	2578	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs761146565;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2580	2580	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs374822197;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2585	2585	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1326049059;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2594	2594	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1276862106;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2597	2597	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs770774164;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2601	2601	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs992941793;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2616	2616	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1326564744;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2622	2622	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1319714625;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2635	2635	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs985595681;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2640	2640	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1393970382;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2647	2647	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1404878473;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2655	2655	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955974070;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2657	2657	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1019400127;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2658	2658	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs780821197;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2662	2662	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs187009810;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2663	2663	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541212507;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2667	2667	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1041667828;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2670	2670	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1167318932;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2671	2671	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1475696264;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2672	2672	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1405598391;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2674	2674	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs918466416;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2675	2675	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1195385529;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2681	2681	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs931250499;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2687	2687	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1418077431;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2694	2694	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1204475602;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2701	2701	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1256548861;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2711	2711	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1195796732;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2718	2718	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1340643287;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2728	2728	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1271484221;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2729	2729	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs753837145;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2745	2745	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs984029791;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2750	2750	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1242015093;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2753	2753	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs916548110;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2758	2758	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs904818644;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2759	2759	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1315323350;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2764	2764	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1366838555;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2766	2766	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1465089486;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2767	2767	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs16939861;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2774	2774	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1327902327;alleles=A%2CC%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2776	2776	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541902389;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2779	2779	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1349791305;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2783	2783	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1040300793;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2803	2803	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs192258080;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2804	2804	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1184502065;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2805	2805	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446668586;alleles=T%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2823	2823	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1281634906;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2824	2824	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1371638005;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2829	2829	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438706527;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2836	2836	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs998731903;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2838	2838	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1275764200;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2842	2843	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1030099529;alleles=-%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2848	2848	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs754485882;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2855	2855	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs369197832;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2860	2860	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906625325;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2872	2872	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs935447272;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2880	2880	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1316025087;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2882	2883	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1168224551;alleles=-%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2885	2885	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1052622495;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2887	2887	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs548833697;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2897	2897	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs894035026;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2900	2900	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1014589512;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2911	2911	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438321414;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2912	2912	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1442698911;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2914	2914	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1011149983;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2916	2916	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs370020780;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2917	2917	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1206537935;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2919	2919	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1404245218;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2922	2922	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1230903280;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2924	2924	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs138084835;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2932	2932	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1034654056;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2936	2936	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1406095157;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2937	2937	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs958585513;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2951	2951	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs537513780;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2953	2955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs771687715;alleles=CCG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	2963	2963	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269034032;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2970	2970	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224099346;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2981	2981	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1350810764;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2985	2985	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283125289;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	2987	2987	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs35368650;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2988	2988	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1272855697;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	2989	2989	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs374358296;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2992	2992	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs925938357;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3012	3012	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs535065893;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3014	3014	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1346048996;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3016	3020	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1410955251;alleles=AAGCA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3037	3037	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs993940078;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3038	3038	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1406881834;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3041	3041	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1343445367;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3045	3045	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs936279227;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3046	3046	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1039969234;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3049	3049	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1410667852;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3056	3056	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs552972231;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3057	3057	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446464723;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3059	3059	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1337855592;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3063	3063	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs952568428;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3068	3068	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1484614726;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3069	3069	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs752361277;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3070	3070	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244138051;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3072	3072	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs934177673;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3073	3073	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1448342009;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3077	3077	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283604944;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3083	3083	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs916534207;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3084	3084	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1216205215;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3085	3085	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs890242585;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3087	3087	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs758034998;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3088	3088	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1204035918;alleles=A%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3089	3089	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs553041259;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3097	3097	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1216704574;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3098	3098	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs982135924;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3114	3114	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1459697651;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3121	3121	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269636882;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3140	3140	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs898846971;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3141	3141	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541738745;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3142	3142	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs935414689;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3146	3146	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1407225788;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3153	3153	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs12449780;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3158	3159	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1356099906;alleles=-%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3161	3161	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs11548428;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3164	3164	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1427254414;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3167	3167	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1034274080;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3168	3178	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1186574299;alleles=GGCTTGTTGCA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3183	3183	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs946908519;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3195	3195	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1461617225;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3197	3197	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs556712929;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3204	3204	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1417962663;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3207	3207	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1202398712;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3216	3216	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs889384859;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3217	3217	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1215270939;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3220	3221	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1364084510;alleles=AG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3230	3230	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1406322662;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3242	3242	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs143759450;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3244	3244	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs977463771;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3245	3245	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1339071335;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3253	3253	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs183449664;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3256	3256	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs900904651;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3259	3259	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs757632957;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3262	3262	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1333781433;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3264	3264	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1411163563;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3265	3265	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1382794105;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3270	3270	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1025384349;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3273	3273	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs781629571;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3274	3274	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1444829035;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3283	3283	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244793198;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3286	3286	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1005390105;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3288	3288	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs975779870;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3289	3289	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1023933916;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3295	3295	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs934227498;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3296	3296	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1051303465;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3301	3301	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs908689377;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3304	3304	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1245603780;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3311	3311	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs564244625;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3312	3312	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1360420160;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3313	3313	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1315035585;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3317	3317	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1390032565;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3321	3322	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs35225641;alleles=-%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3345	3345	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs746408568;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3350	3350	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224119541;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3351	3351	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1299260497;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3366	3366	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs775429324;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3367	3367	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1363250321;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3371	3372	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1264705091;alleles=-%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3375	3375	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1316745110;alleles=C%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3376	3376	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386715308;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3377	3377	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1321174504;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3378	3378	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs769836303;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3379	3379	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1262034984;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3380	3380	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178920999;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3397	3397	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1448418611;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3405	3405	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs775600347;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3406	3406	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs940143966;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3407	3424	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1490514482;alleles=TGACTGACGTTTGCTCCT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3430	3430	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308112860;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3431	3431	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs982492718;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3442	3442	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1431840999;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3447	3447	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs927938344;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3449	3449	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs528068964;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3450	3450	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs956715924;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3458	3458	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs988222284;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3473	3473	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749516447;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3474	3474	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1172397901;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3476	3476	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1385919379;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3496	3496	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs946835113;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3501	3501	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1050620364;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3502	3502	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs910773287;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3504	3504	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs944993602;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3528	3528	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs894433375;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3536	3536	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs540250520;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3539	3539	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1161001321;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3540	3540	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1041047055;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3545	3545	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs774477716;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3548	3548	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs993827034;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3550	3550	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200007511;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3553	3553	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1480815947;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3560	3560	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269527506;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3563	3563	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1203649309;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3570	3570	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1405424311;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3578	3578	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1485660044;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3583	3583	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1285144548;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3584	3584	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs879076610;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3585	3585	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs768824847;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3593	3593	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1046763137;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3594	3594	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1210979641;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3609	3609	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs888199407;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3616	3616	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs560072132;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3618	3618	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs530382672;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3626	3626	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283231811;alleles=A%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3638	3638	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs2269746;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3639	3639	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1332360553;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3640	3640	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1352385209;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3643	3643	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1292818858;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3645	3645	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1033099011;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3659	3660	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1385237938;alleles=-%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3666	3666	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1322059129;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3680	3680	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs957649196;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3682	3682	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1405017960;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3684	3684	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs975471918;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3685	3685	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1481357305;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3686	3686	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1379508682;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3688	3688	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1309733064;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3689	3689	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1028738032;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3706	3706	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1427930374;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3720	3720	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs570223309;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3725	3725	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1023481224;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3726	3726	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs905053344;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3733	3733	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1003444775;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3734	3734	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1490376937;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3742	3743	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1223826001;alleles=CT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3750	3750	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955670344;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3751	3751	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs531175480;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3760	3760	0.0	+	.	consequence_type=splice_acceptor_variant;id=rs908772709;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3761	3761	0.0	+	.	consequence_type=splice_acceptor_variant;id=rs760326328;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3765	3765	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs766296948;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3776	3776	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs974205497;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3777	3777	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs147214037;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3778	3778	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1381816278;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3784	3784	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1415905438;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3786	3786	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1394259462;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3795	3796	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141401145;alleles=-%2CGGG
CDS|ENST00000592782	dbSNP	sequence_variant	3800	3800	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1157100100;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3814	3816	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1461567461;alleles=CTC%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3821	3821	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs968180288;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3826	3826	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1443007106;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3828	3828	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs140336433;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3829	3829	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1359930443;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3831	3831	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs930386786;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3836	3836	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs986678164;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3850	3850	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1249073442;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3856	3856	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs910710077;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3857	3857	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1989802;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3859	3859	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs553298659;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3860	3860	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs142694577;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3861	3861	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386203552;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3862	3862	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs761868545;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3865	3865	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1337321748;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3867	3867	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs574325904;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3871	3871	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1328158733;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3874	3874	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1391867226;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3880	3880	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1371318412;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3886	3886	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs764818146;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3887	3887	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs919516938;alleles=G%2CA%2CC%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3905	3905	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs929604101;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3913	3913	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs187295973;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3914	3914	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs888166470;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3915	3915	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs3214106;alleles=T%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3917	3917	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs397839901;alleles=T%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	3923	3923	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224040282;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3926	3926	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1289033696;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3935	3935	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1253414817;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3936	3936	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs997320577;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3940	3940	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs144416810;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3955	3955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1292084177;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3958	3958	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955369588;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3962	3962	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1348327259;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3966	3966	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs751249150;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3967	3967	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1045241182;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3968	3968	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs755604520;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3979	3979	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs905022668;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3982	3982	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1352271352;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3983	3983	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs77946949;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3984	3984	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1403213945;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	3985	3985	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1439947020;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3992	3992	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs547051568;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3993	3993	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1379886654;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4004	4004	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs892391956;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4005	4005	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs961616835;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4012	4013	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1383339545;alleles=-%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4014	4014	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1158337296;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4017	4017	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs774283266;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4018	4018	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs190636525;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4020	4020	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1457290710;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4022	4022	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1479853735;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4024	4024	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1246754349;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4027	4027	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs565687243;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4028	4028	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs182422410;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4033	4033	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283050785;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4042	4042	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs188355789;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4043	4043	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1444269533;alleles=C%2CA%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4051	4051	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1281320353;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4052	4052	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs539966111;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4058	4058	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs200266826;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4059	4059	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs148432087;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4060	4060	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs542532260;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4062	4062	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1324919529;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4067	4067	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs919485924;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4069	4069	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1312197328;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4075	4075	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1320607191;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4081	4081	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs142546587;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4082	4082	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs150884493;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4086	4086	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs552771831;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4101	4101	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1425334483;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4105	4105	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1192441986;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4107	4107	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1989803;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4109	4109	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs996662517;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4114	4114	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1044812746;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4115	4115	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1989804;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4118	4118	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs939160862;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4120	4120	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1312685053;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4121	4121	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1185666305;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4132	4132	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1221017211;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4144	4144	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1359901535;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4146	4147	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs34744705;alleles=-%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4150	4150	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269886501;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4153	4153	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1254108565;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4156	4156	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1367882615;alleles=C%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4156	4156	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1423351568;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4158	4158	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1335128053;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4160	4160	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1056331855;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4161	4161	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1028830330;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4162	4162	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs139674606;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4172	4172	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1009476590;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4174	4174	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs192155766;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4175	4175	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1418135469;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4176	4176	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs903842957;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4179	4179	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1169691551;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4182	4182	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs961646708;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4186	4186	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1454196689;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4191	4191	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1182764305;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4192	4193	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1377763196;alleles=-%2CCCTCCCAG
CDS|ENST00000592782	dbSNP	sequence_variant	4194	4194	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs780182043;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4195	4197	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1382272062;alleles=TTC%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4200	4201	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1297164419;alleles=-%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4203	4203	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs745510279;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4204	4204	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1202335769;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4214	4214	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs531998526;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4220	4220	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs550454414;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4225	4225	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1229489407;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4238	4238	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs959825452;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4240	4240	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs997609682;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4246	4246	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs569160208;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4247	4247	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs539239556;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4253	4253	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs547487392;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4254	4254	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1305161174;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4255	4255	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1026426534;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4257	4257	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1353484693;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4259	4259	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs557899355;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4265	4265	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308094768;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4266	4266	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs569814923;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4272	4272	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs144545088;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4275	4275	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1431040974;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4282	4282	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1383004525;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4284	4284	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs533836199;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4286	4286	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1424233255;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4287	4287	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1254450780;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4290	4290	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1415662028;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4296	4296	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs12936003;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4297	4297	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541600919;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4301	4301	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs962373075;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4302	4302	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs544254488;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4307	4307	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs563957742;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4309	4309	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs980849596;alleles=G%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4317	4317	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749256414;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4319	4319	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1322740022;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4320	4320	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs575861858;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4322	4322	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs926371390;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4323	4323	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1350420604;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4327	4327	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1470853672;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4338	4338	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1173749197;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4349	4349	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1358196928;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4354	4354	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs939097785;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4355	4356	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1454048669;alleles=TG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4358	4358	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1008298671;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4363	4363	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs778951530;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4375	4375	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs193078436;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4378	4378	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1337790259;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4388	4388	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897173445;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4394	4394	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs995497441;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4397	4397	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1027651561;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4404	4410	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs959615103;alleles=ATGGAAA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4412	4412	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1278151802;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4420	4420	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1346739321;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4423	4423	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1488921375;alleles=C%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4424	4424	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1221273215;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4425	4425	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs945223332;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4434	4437	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1299713857;alleles=CTGT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4440	4440	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1214091270;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4449	4449	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1025095889;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4450	4450	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs903769489;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4455	4455	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs981141232;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4460	4460	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386792118;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4463	4463	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs924334554;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4464	4464	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1007533963;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4472	4472	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1286717016;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4479	4479	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1452821185;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4480	4480	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs770817008;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4481	4481	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs901871985;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4484	4484	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs878981029;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4485	4485	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs989799803;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4487	4487	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1427357837;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4489	4489	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs914510020;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4491	4491	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1215757676;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4505	4505	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs868032669;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4509	4509	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269479940;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4510	4510	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs78867706;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4511	4511	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs546676595;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4513	4513	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749218149;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4514	4514	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1211190168;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4515	4515	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs868806036;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4516	4516	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs943825011;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4517	4517	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1026396864;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4518	4518	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1037137398;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4530	4533	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897205397;alleles=AACC%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4546	4546	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1433862222;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4551	4551	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1365743509;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4561	4561	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1322283760;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4566	4566	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1450115395;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4567	4567	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs950877614;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4574	4574	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1173045404;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4583	4583	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1048382196;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4584	4586	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1379420648;alleles=AGA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4588	4588	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1358022791;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4589	4589	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1449080582;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4595	4595	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs561891221;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4600	4600	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs368287374;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4602	4602	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1006353220;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4610	4610	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs577035381;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4611	4611	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1460229676;alleles=A%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4615	4615	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1418523760;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4621	4621	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1201507011;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4625	4625	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1483970890;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4627	4627	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1303283049;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4629	4629	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1366718155;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4637	4637	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs184426663;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4638	4638	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs550593694;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4647	4647	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs146633312;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4660	4660	0.0	+	.	consequence_type=splice_acceptor_variant;id=rs1339596894;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4661	4661	0.0	+	.	consequence_type=splice_region_variant;id=rs926270475;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4666	4666	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1339338471;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4669	4669	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs12723;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4682	4682	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs762322394;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4691	4691	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs999623239;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4694	4694	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs960386125;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4698	4698	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs991907782;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4701	4701	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1351838802;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4710	4710	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1404515789;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4712	4712	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs913659066;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4721	4721	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1306279725;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4727	4727	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs116783088;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4729	4729	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1391053186;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4730	4730	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955809507;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4733	4733	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs75772115;alleles=C%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4744	4744	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs768617425;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4745	4745	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1021274457;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4752	4752	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs943266937;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4757	4757	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs566620609;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4758	4758	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs534025851;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4769	4769	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs187764117;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4770	4770	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs376074145;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4772	4772	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1355425511;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4776	4778	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438757711;alleles=TGT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4785	4785	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs972526380;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4786	4786	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1047770564;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4803	4803	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1287608514;alleles=T%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4813	4813	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs11548430;alleles=C%2CA%2CG%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4820	4820	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386562475;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4835	4835	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1403810719;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4836	4836	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1390535430;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4838	4838	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1006323540;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4843	4843	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1164212346;alleles=G%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4844	4844	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1473940853;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4848	4848	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs537955893;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4854	4854	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs556169662;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4855	4855	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906062210;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4857	4857	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1349622073;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4862	4862	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1472659160;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4865	4865	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1253304992;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4867	4867	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1002177925;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4892	4892	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs878909110;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4896	4897	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906753161;alleles=-%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4898	4898	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs546438804;alleles=G%2CA%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4901	4901	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446413412;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4908	4908	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1290273986;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4910	4910	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1434321670;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4914	4914	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs991824327;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4917	4917	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1330745525;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4920	4920	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs372498096;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4921	4921	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1011314340;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4931	4931	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386877848;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4940	4940	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1315742111;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4947	4947	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs767858850;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4951	4951	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1458224860;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4960	4960	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1358585731;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4962	4962	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141266275;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4963	4963	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1170305096;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4965	4965	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1477387533;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4966	4966	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1289016599;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4971	4971	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200521307;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4979	4982	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308053456;alleles=AAAG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	4990	4990	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200289824;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4991	4991	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs112206165;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4996	4996	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1236208595;alleles=A%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	14	14	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs925864340;alleles=C%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	17	17	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1179355388;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	20	20	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs924039403;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	51	51	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs921096477;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	55	55	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1483633510;alleles=A%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	60	60	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1164597009;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	68	68	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1469170000;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	68	68	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1420608050;alleles=A%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	88	88	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs750501413;alleles=C%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	88	88	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1018975435;alleles=C%2CA%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	166	166	0.0	+	.	consequence_type=missense_variant;id=rs756082410;alleles=C%2CA%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	167	167	0.0	+	.	consequence_type=synonymous_variant;id=rs780444510;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	168	168	0.0	+	.	consequence_type=missense_variant;id=rs1424340537;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	169	169	0.0	+	.	consequence_type=missense_variant;id=rs973343235;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	171	171	0.0	+	.	consequence_type=missense_variant;id=rs754859910;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	172	172	0.0	+	.	consequence_type=missense_variant;id=rs1356403688;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	175	175	0.0	+	.	consequence_type=missense_variant;id=rs202061902;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	177	177	0.0	+	.	consequence_type=synonymous_variant;id=rs748150811;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	178	178	0.0	+	.	consequence_type=missense_variant;id=rs772038652;alleles=T%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	179	179	0.0	+	.	consequence_type=synonymous_variant;id=rs927228181;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	253	255	0.0	+	.	consequence_type=inframe_deletion;id=rs766213031;alleles=ACA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	256	256	0.0	+	.	consequence_type=missense_variant;id=rs946116469;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	257	257	0.0	+	.	consequence_type=synonymous_variant;id=rs766535198;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1052	1056	0.0	+	.	consequence_type=frameshift_variant;id=rs1056950860;alleles=TGAAG%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1633	1633	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs377286541;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1713	1714	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308084346;alleles=GA%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1942	1943	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs199746970;alleles=-%2CTA
CDS|ENST00000592782	dbSNP	sequence_variant	1943	1943	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955712879;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	1943	1955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs905921677;alleles=TATATATATATAT%2C-
CDS|ENST00000592782	dbSNP	sequence_variant	1944	1944	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1174239154;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	1954	1955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1477157222;alleles=-%2CTT
CDS|ENST00000592782	dbSNP	sequence_variant	1954	1954	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1057096455;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	1955	1955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs914358436;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1956	1956	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1169610627;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	1984	1984	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1470944382;alleles=T%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2139	2139	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1025575332;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2275	2275	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1164637646;alleles=A%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2276	2276	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1485040927;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2277	2277	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs117105863;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2280	2281	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs571677514;alleles=-%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2352	2352	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1041971745;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	2954	2954	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs559020504;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	2955	2955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs917340541;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3159	3159	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1052550601;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3170	3170	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1476082108;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3174	3174	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs915393689;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3372	3372	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1162366452;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3408	3408	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1267486371;alleles=G%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	3410	3410	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1261918292;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3414	3414	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1477740070;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3415	3415	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs762891713;alleles=G%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	3816	3816	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1390845084;alleles=C%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	3857	3858	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1276112396;alleles=-%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4014	4015	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1445524322;alleles=-%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4191	4192	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1300740579;alleles=-%2CCCCAG
CDS|ENST00000592782	dbSNP	sequence_variant	4388	4389	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1156685668;alleles=-%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4410	4410	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs913721217;alleles=A%2CG
CDS|ENST00000592782	dbSNP	sequence_variant	4435	4435	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs2239925;alleles=T%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4450	4451	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs770118889;alleles=-%2CC
CDS|ENST00000592782	dbSNP	sequence_variant	4533	4533	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1293059007;alleles=C%2CA
CDS|ENST00000592782	dbSNP	sequence_variant	4585	4585	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1160866224;alleles=G%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4897	4897	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs192440480;alleles=G%2CA%2CC%2CT
CDS|ENST00000592782	dbSNP	sequence_variant	4897	4897	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1290068700;alleles=G%2C-
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1624	1624	0.0	.	.	AC_Male=1;AF_NFE=8.97215e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-62;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08210e-06;Hom=0;AF_POPMAX=8.97215e-06;AN_POPMAX=111456;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.44524e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=55;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.12258e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=13/13,cDNA_position=1624,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.*2C>G
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1628	1628	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=2.51189e-44;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08614e-06;Hom=0;AF_POPMAX=4.48672e-05;AN_POPMAX=22288;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.45123e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.48837e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.14055e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=T:0,cDNA_position=1628,ExAC_NFE_MAF=T:0.0001512,SYMBOL=NMT1,Existing_variation=rs747853709,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.*6C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1630	1630	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=6.30957e-54;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08707e-06;Hom=0;AF_POPMAX=4.48672e-05;AN_POPMAX=22288;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.45334e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.18605e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92644e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=13/13,cDNA_position=1630,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.*8C>G
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1632	1632	0.0	.	.	AC_Male=4;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|2|1|1|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-26;AF_OTH=0.00000e+00;alleles=A%2CAG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.87102e-05;Hom=0;AF_POPMAX=2.96525e-04;AN_POPMAX=16862;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|1|2|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=2.99039e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=3.70370e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=2.72593e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|6;Hom_raw=0;AF_SAS=6.61638e-05;AS_RF=6.87752e-01;Hom_AMR=0;AC_EAS=5;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.96525e-04;AC_SAS=2;POPMAX=EAS;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84239e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,HGVS_OFFSET=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0.0001156,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=G:0,cDNA_position=1632-1633,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763336808,VARIANT_CLASS=insertion,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592782.1:c.*11dupG,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1633	1633	0.0	.	.	AC_Male=3;AF_NFE=2.69469e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15678e-88;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63716e-05;Hom=0;AF_POPMAX=3.29576e-05;AN_POPMAX=30342;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0;AF_Male=2.23857e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=9.06520e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=3.29576e-05;AS_RF=9.30036e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62425e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:4.496e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=A:0,cDNA_position=1633,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs377286541,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:2.471e-05,HGVSc=ENST00000592782.1:c.*11G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1634	1634	0.0	.	.	AC_Male=1;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-91;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09195e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.46035e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.16667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=60;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.46101e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=13/13,cDNA_position=1634,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.*12T>A
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1636	1636	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.84034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10071e-06;Hom=0;AF_POPMAX=3.04099e-05;AN_POPMAX=32884;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.47507e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.77311e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.43019e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=3.04099e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=13/13,cDNA_position=1636,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.*14C>T
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1637	1637	0.0	.	.	AC_Male=2;AF_NFE=2.70100e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|0|0|0|0|0|3|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=2.50594e-46;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=4.49115e-05;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.05460e-05;Hom=0;AF_POPMAX=6.57981e-05;AN_POPMAX=15198;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|2|0|0|0|0|2|0|1|0|0|0|1|0|0|0|0|0;AF_Male=1.49788e-05;AF_AFR=6.57981e-05;AC_raw=6;AB_MEDIAN=4.35216e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=2.73139e-05;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.16709e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:4.12e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.998e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0002,Allele=A,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=A:9.614e-05,cDNA_position=1637,ExAC_NFE_MAF=A:0.0001512,SYMBOL=NMT1,Existing_variation=rs370761943,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:4.118e-05,HGVSc=ENST00000592782.1:c.*15G>A,ExAC_Adj_MAF=A:8.643e-05
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1640	1640	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-68;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10624e-06;Hom=0;AF_POPMAX=6.57376e-05;AN_POPMAX=15212;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48413e-06;AF_AFR=6.57376e-05;AC_raw=1;AB_MEDIAN=5.38462e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.02328e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=C:9.615e-05,cDNA_position=1640,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs756865994,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.*18T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1643	1643	0.0	.	.	AC_Male=61593;AF_NFE=4.22062e-01;Hom_FIN=2448;GQ_MEDIAN=99;AB_HIST_ALT=0|2|56|292|736|1976|4000|7432|12641|12024|11096|4916|2284|797|303|124|43|27|28|0;AC_FIN=10454;DREF_MEDIAN=3.98107e-70;AF_OTH=4.62645e-01;alleles=G%2CA;AF_FIN=4.70689e-01;AC_OTH=2477;Hom_Male=14819;AC=112061;Hom_NFE=9865;AF=4.62481e-01;Hom=27067;AF_POPMAX=7.72167e-01;AN_POPMAX=16714;AC_NFE=46724;AS_FilterStatus=PASS;Hom_OTH=591;DP_HIST_ALT=26|1062|5268|9353|8716|6312|4899|4852|5720|6174|6017|5529|4737|3912|2917|2209|1744|1260|974|952;AF_Male=4.63210e-01;AF_AFR=3.48249e-01;AC_raw=114295;AB_MEDIAN=4.57627e-01;Hom_EAS=4996;AC_AMR=15494;AF_ASJ=4.67235e-01;DP_MEDIAN=42;AF_Female=4.61595e-01;GQ_HIST_ALT=23|40|51|158|301|286|785|1226|826|1543|1574|913|1410|1167|657|1035|863|585|831|72262;Hom_raw=27759;AF_SAS=4.72870e-01;AS_RF=9.54732e-01;Hom_AMR=3731;AC_EAS=12906;AC_Female=50468;Hom_AFR=919;Hom_ASJ=1055;AF_EAS=7.72167e-01;AC_SAS=14188;POPMAX=EAS;AC_POPMAX=12906;AC_AFR=5269;Hom_SAS=3462;AC_ASJ=4549;AF_raw=4.64104e-01;Hom_Female=12248;AF_AMR=4.77444e-01;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.4574,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.4308,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0.3321,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.4239,AFR_MAF=A:0.4771,SWISSPROT=P30419,EAS_MAF=A:0.4755,EUR_MAF=A:0.7946,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0.7698,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,GMAF=G:0.4940,STRAND=1,ExAC_SAS_MAF=A:0.4713,CCDS=CCDS11494.1,EA_MAF=A:0.3423,Allele=A,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=A:0.3473,cDNA_position=1643,ExAC_NFE_MAF=A:0.4712,SYMBOL=NMT1,Existing_variation=rs1053733,SAS_MAF=A:0.4712,VARIANT_CLASS=SNV,AA_MAF=A:0.501,MINIMISED=1,ExAC_AFR_MAF=A:0.457,HGVSc=ENST00000592782.1:c.*21G>A,ExAC_Adj_MAF=A:0.4795
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1652	1652	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.14817e-06;Hom=0;AF_POPMAX=3.14327e-05;AN_POPMAX=31814;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.81481e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.19709e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20180e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=3.14327e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=13/13,cDNA_position=1652,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.*30C>T
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1659	1659	0.0	.	.	AC_Male=1;AF_NFE=2.71474e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-30;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.24726e-05;Hom=0;AF_POPMAX=2.71474e-05;AN_POPMAX=110508;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.57083e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.84430e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.36557e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.246e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=T:0,cDNA_position=1659,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749639976,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592782.1:c.*37A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1663	1663	0.0	.	.	AC_Male=2;AF_NFE=2.71493e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|2|0|1|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-63;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.66312e-05;Hom=0;AF_POPMAX=6.60328e-05;AN_POPMAX=15144;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|1|0;AF_Male=1.51435e-05;AF_AFR=6.60328e-05;AC_raw=5;AB_MEDIAN=3.26087e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=1.84430e-05;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.31532e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03029e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:3.3e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.501e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=T:9.639e-05,cDNA_position=1663,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs769028747,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000592782.1:c.*41C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	3_prime_UTR_variant	1664	1664	0.0	.	.	AC_Male=6;AF_NFE=9.01599e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|1|1|1|0|3|2|4|4|2|2|3|1|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-31;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=22;Hom_NFE=0;AF=9.08033e-05;Hom=0;AF_POPMAX=1.23508e-03;AN_POPMAX=9716;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|6|2|5|2|1|2|1|0|1|1|1|0|1|1|0|0|0|0;AF_Male=4.51155e-05;AF_AFR=5.28053e-04;AC_raw=25;AB_MEDIAN=4.31034e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.23508e-03;DP_MEDIAN=24;AF_Female=1.46399e-04;GQ_HIST_ALT=1|0|1|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|2|19;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.85325e-01;Hom_AMR=0;AC_EAS=1;AC_Female=16;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.00601e-05;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=12;AC_AFR=8;Hom_SAS=0;AC_ASJ=12;AF_raw=1.01514e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:4.95e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:4.501e-05,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0.001,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000468424,Consequence=3_prime_UTR_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0002,Allele=A,IMPACT=MODIFIER,EXON=13/13,ExAC_AMR_MAF=A:0.0001927,cDNA_position=1664,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs371753337,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:4.942e-05,HGVSc=ENST00000592782.1:c.*42G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	inframe_deletion	252	255	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-19;AF_OTH=0.00000e+00;alleles=TACA%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63922e-05;Hom=0;AF_POPMAX=2.63817e-04;AN_POPMAX=15162;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24225e-05;AF_AFR=2.63817e-04;AC_raw=4;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07243e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.21158e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=4;AC_AFR=4;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=-:3.614e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=-:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=-:0,AFR_MAF=-:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=2,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=-:0,ENSP=ENSP00000468424,Consequence=inframe_deletion,Amino_acids=YN/Y,HGVSp=ENSP00000468424.1:p.Asn42del,STRAND=1,ExAC_SAS_MAF=-:0,CCDS=CCDS11494.1,EA_MAF=-:0.0007,Allele=-,IMPACT=MODERATE,EXON=2/13,ExAC_AMR_MAF=-:0.0004244,cDNA_position=253-255,CDS_position=122-124,ExAC_NFE_MAF=-:0,SYMBOL=NMT1,Existing_variation=rs766213031,VARIANT_CLASS=deletion,Protein_position=41-42,Codons=tACAac/tac,MINIMISED=1,ExAC_AFR_MAF=-:3.295e-05,HGVSc=ENST00000592782.1:c.124_126delAAC,ExAC_Adj_MAF=-:0
CDS|ENST00000592782	VCF	splice_region_variant	85	85	0.0	.	.	AC_Male=1;AF_NFE=9.93700e-06;Hom_FIN=0;GQ_MEDIAN=54;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.54545e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.56955e-06;Hom=0;AF_POPMAX=9.93700e-06;AN_POPMAX=100634;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=8.26610e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.26923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.37054e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12334e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:9.138e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.645e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=splice_region_variant&5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=85,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs763044000,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.238e-06,HGVSc=ENST00000592782.1:c.-47G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	splice_region_variant	260	260	0.0	.	.	AC_Male=4;AF_NFE=2.73010e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25597e-29;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.64955e-05;Hom=0;AF_POPMAX=6.65513e-05;AN_POPMAX=15026;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=3.00680e-05;AF_AFR=6.65513e-05;AC_raw=4;AB_MEDIAN=5.27778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.27137e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62425e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:9.22e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=C:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.668e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=splice_region_variant&synonymous_variant,Amino_acids=R,HGVSp=ENST00000592782.1:c.129G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=C:0,Allele=A,IMPACT=LOW,EXON=2/13,ExAC_AMR_MAF=A:0,cDNA_position=260,CDS_position=129,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs143955814,VARIANT_CLASS=SNV,Protein_position=43,Codons=cgG/cgA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.129G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	splice_region_variant	518	518	0.0	.	.	AC_Male=1;AF_NFE=8.98699e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.49763e-52;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13974e-06;Hom=0;AF_POPMAX=2.97992e-05;AN_POPMAX=33558;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43030e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.59152e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.29846e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.318e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=splice_region_variant&synonymous_variant,GMAF=A:0.0002,Amino_acids=G,HGVSp=ENST00000592782.1:c.387C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=518,CDS_position=387,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=129,AA_MAF=A:0,Codons=ggC/ggT,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.387C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	splice_region_variant	518	518	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=60;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.13501e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06987e-06;Hom=0;AF_POPMAX=6.53766e-05;AN_POPMAX=15296;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53766e-05;AC_raw=2;AB_MEDIAN=3.53758e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.07429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.318e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=splice_region_variant&synonymous_variant,GMAF=A:0.0002,Amino_acids=G,HGVSp=ENST00000592782.1:c.387C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=5/13,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=518,CDS_position=387,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=129,AA_MAF=A:0,Codons=ggC/ggA,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592782.1:c.387C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	splice_region_variant	845	845	0.0	.	.	AC_Male=0;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07040e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.75083e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=301;AF_Female=9.00009e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.23711e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.3e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.507e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=splice_region_variant&synonymous_variant,Amino_acids=T,HGVSp=ENST00000592782.1:c.714A>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=8/13,ExAC_AMR_MAF=C:0,cDNA_position=845,CDS_position=714,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs752735481,VARIANT_CLASS=SNV,Protein_position=238,Codons=acA/acC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592782.1:c.714A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	splice_region_variant	1298	1298	0.0	.	.	AC_Male=26;AF_NFE=4.54298e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|7|24|25|20|7|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25657e-177;AF_OTH=1.85185e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=88;Hom_NFE=0;AF=3.61869e-04;Hom=1;AF_POPMAX=3.92567e-03;AN_POPMAX=15284;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|3|2|2|3|4|4|2|8|2|1|2|1|1|1|0|2|0;AF_Male=1.95298e-04;AF_AFR=3.92567e-03;AC_raw=89;AB_MEDIAN=4.71698e-01;Hom_EAS=0;AC_AMR=19;AF_ASJ=2.09380e-04;DP_MEDIAN=124;AF_Female=5.63370e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|88;Hom_raw=1;AF_SAS=3.29707e-05;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=62;Hom_AFR=1;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=60;AC_AFR=60;Hom_SAS=0;AC_ASJ=2;AF_raw=3.61392e-04;Hom_Female=1;AF_AMR=5.71738e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,AMR_MAF=T:0.0061,Gene=ENSG00000136448,HGNC_ID=7857,EAS_MAF=T:0,SYMBOL_SOURCE=HGNC,CANONICAL=YES,Consequence=splice_region_variant&synonymous_variant,GMAF=T:0.0016,ExAC_SAS_MAF=T:0.001152,SOMATIC=0&1,IMPACT=LOW,ExAC_AMR_MAF=T:0.004244,CDS_position=1167,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs142226258&COSM1383765,VARIANT_CLASS=SNV,Protein_position=389,AA_MAF=T:0,Codons=aaC/aaT,ExAC_Adj_MAF=T:0.0005195,PHENO=0&1,ExAC_EAS_MAF=T:0.000468,ExAC_MAF=T:0.0005,BIOTYPE=protein_coding,ExAC_OTH_MAF=T:6.085e-05,AFR_MAF=T:0,SWISSPROT=P30419,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Amino_acids=N,HGVSp=ENST00000592782.1:c.1167C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,EA_MAF=T:0.0054,Allele=T,EXON=11/13,cDNA_position=1298,SAS_MAF=T:0,MINIMISED=1,ExAC_AFR_MAF=T:4.612e-04,HGVSc=ENST00000592782.1:c.1167C>T
CDS|ENST00000592782	VCF	5_prime_UTR_variant	87	88	0.0	.	.	AC_Male=16;AF_NFE=7.90498e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|2|0|3|4|3|8|2|9|4|3|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.31559e-19;AF_OTH=0.00000e+00;alleles=AC%2CACC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=28;Hom_NFE=0;AF=1.27423e-04;Hom=0;AF_POPMAX=4.96463e-04;AN_POPMAX=16114;AC_NFE=8;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|10|6|5|6|6|4|2|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.31735e-04;AF_AFR=1.38122e-04;AC_raw=41;AB_MEDIAN=4.47368e-01;Hom_EAS=0;AC_AMR=10;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=1.22095e-04;GQ_HIST_ALT=0|0|0|1|0|1|0|1|3|3|0|0|0|0|2|0|0|0|1|28;Hom_raw=1;AF_SAS=0.00000e+00;AS_RF=7.26242e-01;Hom_AMR=0;AC_EAS=8;AC_Female=12;Hom_AFR=0;Hom_ASJ=0;AF_EAS=4.96463e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=8;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=1.66526e-04;Hom_Female=0;AF_AMR=3.65979e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,HGVS_OFFSET=5,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=2/13,cDNA_position=88-89,SYMBOL=NMT1,Existing_variation=rs750501413,VARIANT_CLASS=insertion,MINIMISED=1,HGVSc=ENST00000592782.1:c.-39dupC
CDS|ENST00000592782	VCF	5_prime_UTR_variant	87	88	0.0	.	.	AC_Male=3;AF_NFE=3.95249e-05;Hom_FIN=0;GQ_MEDIAN=28;AB_HIST_ALT=0|1|3|2|0|1|0|1|0|0|2|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58239e-03;AF_OTH=0.00000e+00;alleles=AC%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.82033e-05;Hom=0;AF_POPMAX=3.95249e-05;AN_POPMAX=101202;AC_NFE=4;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|1|2|3|2|1|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.47003e-05;AF_AFR=0.00000e+00;AC_raw=11;AB_MEDIAN=1.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=1.01746e-05;GQ_HIST_ALT=2|0|1|2|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.42932e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46777e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,HGVS_OFFSET=5,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,CCDS=CCDS11494.1,Allele=-,IMPACT=MODIFIER,EXON=2/13,cDNA_position=88,SYMBOL=NMT1,Existing_variation=rs750501413,VARIANT_CLASS=insertion,MINIMISED=1,HGVSc=ENST00000592782.1:c.-39delC
CDS|ENST00000592782	VCF	5_prime_UTR_variant	93	93	0.0	.	.	AC_Male=1;AF_NFE=9.45734e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-39;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.28964e-06;Hom=0;AF_POPMAX=9.45734e-06;AN_POPMAX=105738;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.78986e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.90051e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06081e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.086e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.635e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=93,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs768711397,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.238e-06,HGVSc=ENST00000592782.1:c.-39C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	94	94	0.0	.	.	AC_Male=0;AF_NFE=9.38897e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-28;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.25485e-06;Hom=0;AF_POPMAX=9.38897e-06;AN_POPMAX=106508;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=9.45984e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.41130e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.064e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.631e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=94,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774371000,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.238e-06,HGVSc=ENST00000592782.1:c.-38A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	95	95	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-17;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.24820e-06;Hom=0;AF_POPMAX=6.71501e-05;AN_POPMAX=14892;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.71938e-06;AF_AFR=6.71501e-05;AC_raw=1;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06065e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:9.059e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0002,Allele=A,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=A:0.0001098,cDNA_position=95,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs370358129,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.238e-06,HGVSc=ENST00000592782.1:c.-37T>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	97	97	0.0	.	.	AC_Male=1;AF_NFE=9.32679e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-15;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.22215e-06;Hom=0;AF_POPMAX=9.32679e-06;AN_POPMAX=107218;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.67919e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.84615e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=13;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.12256e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06065e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=2/13,cDNA_position=97,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-35T>A
CDS|ENST00000592782	VCF	5_prime_UTR_variant	98	98	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-51;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.21660e-06;Hom=0;AF_POPMAX=5.90179e-05;AN_POPMAX=16944;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.20690e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=9.36575e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18010e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.90179e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06065e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,cDNA_position=98,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-34A>G
CDS|ENST00000592782	VCF	5_prime_UTR_variant	99	99	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-21;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.21077e-06;Hom=0;AF_POPMAX=5.89831e-05;AN_POPMAX=16954;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=9.34772e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.61962e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.89831e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.034e-06&C:9.034e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.626e-05&C:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&C:0.0001205,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0&C:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=C,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0&C:0,cDNA_position=99,ExAC_NFE_MAF=T:0&C:0,SYMBOL=NMT1,Existing_variation=rs374273277,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.238e-06&C:8.238e-06,HGVSc=ENST00000592782.1:c.-33G>C,ExAC_Adj_MAF=T:0&C:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	99	99	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-40;AF_OTH=1.90621e-04;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.21077e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.66237e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.17241e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.79971e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.034e-06&C:9.034e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.626e-05&C:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&C:0.0001205,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0&C:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0&C:0,cDNA_position=99,ExAC_NFE_MAF=T:0&C:0,SYMBOL=NMT1,Existing_variation=rs374273277,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.238e-06&C:8.238e-06,HGVSc=ENST00000592782.1:c.-33G>T,ExAC_Adj_MAF=T:0&C:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	101	101	0.0	.	.	AC_Male=1;AF_NFE=9.28747e-06;Hom_FIN=0;GQ_MEDIAN=29;AB_HIST_ALT=0|0|1|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25734e-03;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20355e-06;Hom=0;AF_POPMAX=9.28747e-06;AN_POPMAX=107672;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.65181e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.53846e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.24195e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21819e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.804e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.246e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=101,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs373569442,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.-31G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	102	102	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-24;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.40421e-06;Hom=0;AF_POPMAX=1.17758e-04;AN_POPMAX=16984;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=1.86473e-05;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.53170e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.17758e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21819e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=2/13,cDNA_position=102,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-30G>A
CDS|ENST00000592782	VCF	5_prime_UTR_variant	103	103	0.0	.	.	AC_Male=3;AF_NFE=1.85189e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|2|1|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.30594e-39;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.51482e-05;Hom=0;AF_POPMAX=1.24626e-04;AN_POPMAX=32096;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|3|1|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.28938e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.66935e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=2.78950e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.75580e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43639e-05;Hom_Female=0;AF_AMR=1.24626e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.698e-05&T:8.995e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.239e-05&T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0&T:0.0001202,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=A:0&T:0,cDNA_position=103,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs765574685,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:2.471e-05&T:8.237e-06,HGVSc=ENST00000592782.1:c.-29G>A,ExAC_Adj_MAF=A:9.188e-05&T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	103	103	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-23;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.38272e-06;Hom=0;AF_POPMAX=1.17675e-04;AN_POPMAX=16996;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.63126e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.65103e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=9.29835e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.03256e-01;Hom_AMR=0;AC_EAS=2;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.17675e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.698e-05&T:8.995e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.239e-05&T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0&T:0.0001202,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=A:0&T:0,cDNA_position=103,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs765574685,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:2.471e-05&T:8.237e-06,HGVSc=ENST00000592782.1:c.-29G>T,ExAC_Adj_MAF=A:9.188e-05&T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	105	105	0.0	.	.	AC_Male=9;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|2|2|1|0|1|2|2|1|2|3|2|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-25;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.85990e-05;Hom=0;AF_POPMAX=7.32064e-04;AN_POPMAX=15026;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|4|4|0|5|3|0|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=6.86059e-05;AF_AFR=7.32064e-04;AC_raw=19;AB_MEDIAN=4.03846e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=4.64132e-05;GQ_HIST_ALT=1|1|2|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.01027e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=11;AC_AFR=11;Hom_SAS=0;AC_ASJ=0;AF_raw=7.71517e-05;Hom_Female=0;AF_AMR=9.27873e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.098e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000592782,BIOTYPE=protein_coding,AMR_MAF=A:0.0015,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=A:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,GMAF=A:0.0004,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0005,Allele=A,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=A:0.0009764,cDNA_position=105,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs369298290,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:7.414e-05,HGVSc=ENST00000592782.1:c.-27C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	106	106	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38634e-02;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.16628e-06;Hom=0;AF_POPMAX=5.85549e-05;AN_POPMAX=17078;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.22464e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=9.23532e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.85730e-02;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.85549e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.972e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0.0001203,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=106,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778268422,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000592782.1:c.-26G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	107	107	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-14;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.16639e-06;Hom=0;AF_POPMAX=3.30426e-05;AN_POPMAX=30264;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.59313e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.94118e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.30426e-05;AS_RF=1.73138e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06065e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,cDNA_position=107,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-25C>G
CDS|ENST00000592782	VCF	5_prime_UTR_variant	111	111	0.0	.	.	AC_Male=7;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|1|0|0|0|1|0|3|3|0|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.60110e-30;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=10;Hom_NFE=0;AF=4.13162e-05;Hom=0;AF_POPMAX=3.03251e-04;AN_POPMAX=32976;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|3|3|4|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=5.27275e-05;AF_AFR=0.00000e+00;AC_raw=12;AB_MEDIAN=4.89130e-01;Hom_EAS=0;AC_AMR=10;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=2.74529e-05;GQ_HIST_ALT=0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|10;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06062e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=10;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.87278e-05;Hom_Female=0;AF_AMR=3.03251e-04;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,cDNA_position=111,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-21G>T
CDS|ENST00000592782	VCF	5_prime_UTR_variant	113	113	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-32;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12722e-06;Hom=0;AF_POPMAX=3.27761e-05;AN_POPMAX=30510;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.52445e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.07407e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.27761e-05;AS_RF=8.34415e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.869e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=113,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs752016137,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000592782.1:c.-19C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	114	114	0.0	.	.	AC_Male=4;AF_NFE=5.46847e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|1|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-22;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.47361e-05;Hom=0;AF_POPMAX=5.46847e-05;AN_POPMAX=109720;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|3|0|1|0|1|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=3.00684e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=3.58974e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.82598e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.13304e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43637e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.853e-06&G:4.427e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.596e-05&G:7.98e-05,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0&G:0,cDNA_position=114,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs757362692,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.237e-06&G:4.119e-05,HGVSc=ENST00000592782.1:c.-18C>G,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	114	114	0.0	.	.	AC_Male=0;AF_NFE=1.82282e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-46;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.23681e-05;Hom=0;AF_POPMAX=3.27504e-05;AN_POPMAX=30534;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.14706e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=2.73898e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=3.27504e-05;AS_RF=9.04746e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21819e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.853e-06&G:4.427e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.596e-05&G:7.98e-05,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0&G:0,cDNA_position=114,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs757362692,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.237e-06&G:4.119e-05,HGVSc=ENST00000592782.1:c.-18C>T,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	115	115	0.0	.	.	AC_Male=1;AF_NFE=9.10929e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-30;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12103e-06;Hom=0;AF_POPMAX=9.10929e-06;AN_POPMAX=109778;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.51292e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.23810e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05854e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.842e-06&G:5.305e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.594e-05&G:7.972e-05,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0&G:0.0001195,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0&G:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=C:0&G:0,cDNA_position=115,ExAC_NFE_MAF=C:0&G:0,SYMBOL=NMT1,Existing_variation=rs746125540,VARIANT_CLASS=SNV,ExAC_AFR_MAF=C:8.237e-06&G:4.942e-05,HGVSc=ENST00000592782.1:c.-17T>C,ExAC_Adj_MAF=C:0&G:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	115	115	0.0	.	.	AC_Male=5;AF_NFE=5.46558e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|2|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-47;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.88472e-05;Hom=0;AF_POPMAX=5.83022e-05;AN_POPMAX=17152;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|2|1|1|0|1|0|2|0|0|0|0|0|0|0|0|0|0;AF_Male=3.75646e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=3.84615e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=1.82558e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43112e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.83022e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84243e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.842e-06&G:5.305e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.594e-05&G:7.972e-05,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0&G:0.0001195,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0&G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=C:0&G:0,cDNA_position=115,ExAC_NFE_MAF=C:0&G:0,SYMBOL=NMT1,Existing_variation=rs746125540,VARIANT_CLASS=SNV,ExAC_AFR_MAF=C:8.237e-06&G:4.942e-05,HGVSc=ENST00000592782.1:c.-17T>G,ExAC_Adj_MAF=C:0&G:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	116	116	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=29;AB_HIST_ALT=0|0|1|0|2|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=2;DREF_MEDIAN=6.27931e-03;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=9.09422e-05;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.23676e-06;Hom=0;AF_POPMAX=9.09422e-05;AN_POPMAX=21992;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.50649e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=9.12442e-06;GQ_HIST_ALT=0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.00131e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=2/13,cDNA_position=116,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-16G>A
CDS|ENST00000592782	VCF	5_prime_UTR_variant	117	117	0.0	.	.	AC_Male=1;AF_NFE=9.10382e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-84;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.11838e-06;Hom=0;AF_POPMAX=9.10382e-06;AN_POPMAX=109844;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.51021e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.76271e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=59;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.78031e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,cDNA_position=117,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-15C>G
CDS|ENST00000592782	VCF	5_prime_UTR_variant	118	118	0.0	.	.	AC_Male=1;AF_NFE=1.81663e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97631e-35;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.22253e-06;Hom=0;AF_POPMAX=1.81663e-05;AN_POPMAX=110094;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49625e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.69388e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.10465e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.65455e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.802e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.588e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=C:0,cDNA_position=118,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs779782774,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000592782.1:c.-14T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	119	119	0.0	.	.	AC_Male=1;AF_NFE=1.81683e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97631e-35;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.22423e-06;Hom=0;AF_POPMAX=1.81683e-05;AN_POPMAX=110082;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49704e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.69388e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.10763e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.64758e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.796e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.588e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=119,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749106795,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000592782.1:c.-13C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	121	121	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-25;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.22037e-06;Hom=0;AF_POPMAX=6.52827e-05;AN_POPMAX=30636;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.49894e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.52827e-05;AS_RF=7.90407e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.756e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0001323,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=T:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=T:0,cDNA_position=121,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs768521050,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592782.1:c.-11C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	122	122	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-28;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10971e-06;Hom=0;AF_POPMAX=3.26456e-05;AN_POPMAX=30632;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49221e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.26316e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.26456e-05;AS_RF=8.77261e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=2/13,cDNA_position=122,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-10G>C
CDS|ENST00000592782	VCF	5_prime_UTR_variant	127	127	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-38;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09396e-06;Hom=0;AF_POPMAX=3.25797e-05;AN_POPMAX=30694;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46425e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25797e-05;AS_RF=8.95290e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.698e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=G:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=G:0,cDNA_position=127,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774460908,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592782.1:c.-5T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592782	VCF	5_prime_UTR_variant	129	129	0.0	.	.	AC_Male=0;AF_NFE=9.03653e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-42;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.18371e-06;Hom=0;AF_POPMAX=3.00282e-05;AN_POPMAX=33302;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.85556e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.81238e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.38885e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=3.00282e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.678e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ExAC_FIN_MAF=C:0,ENSP=ENSP00000468424,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=2/13,ExAC_AMR_MAF=C:0,cDNA_position=129,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs748067291,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000592782.1:c.-3A>C,ExAC_Adj_MAF=C:8.983e-05
CDS|ENST00000592782	VCF	5_prime_UTR_variant	131	131	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=13;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.77267e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.86832e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=2/13,cDNA_position=131,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-1G>A
CDS|ENST00000592782	VCF	5_prime_UTR_variant	88	88	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-58;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.53108e-06;Hom=0;AF_POPMAX=6.89750e-05;AN_POPMAX=14498;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.89750e-05;AC_raw=1;AB_MEDIAN=7.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.01303e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.95852e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06187e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,CANONICAL=YES,ENSP=ENSP00000468424,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000592782,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=2/13,cDNA_position=88,SYMBOL=NMT1,Gene=ENSG00000136448,Existing_variation=rs750501413,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592782.1:c.-44C>G
CDS|ENST00000258960	VCF	inframe_insertion	76	76	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-72;AF_OTH=1.82548e-04;alleles=A%2CAGGGAAC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07030e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42611e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.09091e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.02292e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=14,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=inframe_insertion,Amino_acids=-/GN,HGVSp=ENSP00000258960.2:p.Asn25_Gly26dup,STRAND=1,CCDS=CCDS11494.1,Allele=GGGAAC,IMPACT=MODERATE,EXON=1/12,cDNA_position=81-82,CDS_position=63-64,SYMBOL=NMT1,VARIANT_CLASS=insertion,Protein_position=21-22,Codons=-/GGGAAC,MINIMISED=1,HGVSc=ENST00000258960.2:c.72_77dupGAACGG
CDS|ENST00000258960	VCF	inframe_insertion	86	86	0.0	.	.	AC_Male=5;AF_NFE=5.38871e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|2|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=5.01187e-60;AF_OTH=0.00000e+00;alleles=A%2CAACGGCC;AF_FIN=4.48994e-05;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84877e-05;Hom=0;AF_POPMAX=5.38871e-05;AN_POPMAX=111344;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|2|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=3.71261e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=3.80952e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80109e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.11301e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84241e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=ACGGCC:2.556e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=ACGGCC:4.635e-05,AFR_MAF=ACGGCC:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=ACGGCC:0,ENSP=ENSP00000258960,Consequence=inframe_insertion,Amino_acids=N/NGH,HGVSp=ENSP00000258960.2:p.Gly26_His27dup,STRAND=1,ExAC_SAS_MAF=ACGGCC:0,CCDS=CCDS11494.1,Allele=ACGGCC,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=ACGGCC:0,cDNA_position=91-92,CDS_position=73-74,ExAC_NFE_MAF=ACGGCC:0,SYMBOL=NMT1,Existing_variation=rs763191382,VARIANT_CLASS=insertion,Protein_position=25,Codons=aac/aACGGCCac,MINIMISED=1,ExAC_AFR_MAF=ACGGCC:2.471e-05,HGVSc=ENST00000258960.2:c.75_80dupCGGCCA,ExAC_Adj_MAF=ACGGCC:0
CDS|ENST00000258960	VCF	synonymous_variant	31	31	0.0	.	.	AC_Male=3;AF_NFE=3.60536e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|3|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00010e-44;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44872e-05;Hom=0;AF_POPMAX=5.96516e-05;AN_POPMAX=33528;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|2|1|0|0|0|1|0|0|0|0|0|0;AF_Male=2.23125e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.54132e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=2.71316e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43635e-05;Hom_Female=0;AF_AMR=5.96516e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:3.427e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:6.219e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000258960.2:c.18G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=36,CDS_position=18,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs776210749,VARIANT_CLASS=SNV,Protein_position=6,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000258960.2:c.18G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	37	37	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16473e-06;Hom=0;AF_POPMAX=6.50407e-05;AN_POPMAX=30750;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43837e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=6.00160e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50407e-05;AS_RF=9.41280e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000258960.2:c.24A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=1/12,cDNA_position=42,CDS_position=24,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=gcA/gcG,HGVSc=ENST00000258960.2:c.24A>G
CDS|ENST00000258960	VCF	synonymous_variant	37	37	0.0	.	.	AC_Male=0;AF_NFE=9.01534e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-23;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08237e-06;Hom=0;AF_POPMAX=9.01534e-06;AN_POPMAX=110922;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.51046e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000258960.2:c.24A>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=1/12,cDNA_position=42,CDS_position=24,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=gcA/gcC,HGVSc=ENST00000258960.2:c.24A>C
CDS|ENST00000258960	VCF	synonymous_variant	43	43	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-133;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08523e-06;Hom=0;AF_POPMAX=3.25373e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.44225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.78313e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=83;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25373e-05;AS_RF=8.78960e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.561e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=K,HGVSp=ENST00000258960.2:c.30G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=48,CDS_position=30,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs757761311,VARIANT_CLASS=SNV,Protein_position=10,Codons=aaG/aaA,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000258960.2:c.30G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	49	49	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-56;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16067e-06;Hom=0;AF_POPMAX=6.50745e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48723e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.23810e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50745e-05;AS_RF=8.94107e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.542e-06&C:8.542e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0&C:1.55e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.36G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&C:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=T:0&C:0,cDNA_position=54,CDS_position=36,ExAC_NFE_MAF=T:0&C:0,SYMBOL=NMT1,Existing_variation=rs780444510,VARIANT_CLASS=SNV,Protein_position=12,Codons=ccG/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06&C:8.237e-06,HGVSc=ENST00000258960.2:c.36G>T,ExAC_Adj_MAF=T:0&C:0
CDS|ENST00000258960	VCF	synonymous_variant	59	59	0.0	.	.	AC_Male=1;AF_NFE=2.69721e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-37;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22188e-05;Hom=0;AF_POPMAX=2.69721e-05;AN_POPMAX=111226;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.42843e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.80333e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97663e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.515e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.545e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.46C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=64,CDS_position=46,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs748150811,VARIANT_CLASS=SNV,Protein_position=16,Codons=Ctg/Ttg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.46C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	67	67	0.0	.	.	AC_Male=0;AF_NFE=8.98828e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-59;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07106e-06;Hom=0;AF_POPMAX=8.98828e-06;AN_POPMAX=111256;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.77273e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00982e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05614e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=Q,HGVSp=ENST00000258960.2:c.54G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=1/12,cDNA_position=72,CDS_position=54,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=18,Codons=caG/caA,MINIMISED=1,HGVSc=ENST00000258960.2:c.54G>A
CDS|ENST00000258960	VCF	synonymous_variant	112	112	0.0	.	.	AC_Male=0;AF_NFE=9.00236e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.84034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07857e-06;Hom=0;AF_POPMAX=9.00236e-06;AN_POPMAX=111082;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.63736e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=13;AF_Female=9.02543e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.58906e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.666e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.57e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=C,HGVSp=ENST00000258960.2:c.99C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=117,CDS_position=99,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs762294220,VARIANT_CLASS=SNV,Protein_position=33,Codons=tgC/tgT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.99C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	115	115	0.0	.	.	AC_Male=0;AF_NFE=1.80050e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-23;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15614e-06;Hom=0;AF_POPMAX=1.80050e-05;AN_POPMAX=111080;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.76923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=1.80473e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.41561e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.741e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.152e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000258960.2:c.102G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=120,CDS_position=102,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768076232,VARIANT_CLASS=SNV,Protein_position=34,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000258960.2:c.102G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	124	124	0.0	.	.	AC_Male=0;AF_NFE=9.01567e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.22517e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08407e-06;Hom=0;AF_POPMAX=9.01567e-06;AN_POPMAX=110918;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.97806e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.57456e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000258960.2:c.111G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=1/12,cDNA_position=129,CDS_position=111,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=37,Codons=gaG/gaA,MINIMISED=1,HGVSc=ENST00000258960.2:c.111G>A
CDS|ENST00000258960	VCF	synonymous_variant	133	133	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-88;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=1.02270e-04;AN_POPMAX=9778;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.40984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.02270e-04;DP_MEDIAN=61;AF_Female=9.06914e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.25490e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.018e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.120C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=138,CDS_position=120,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=40,Codons=agC/agT,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.120C>T,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	139	139	0.0	.	.	AC_Male=9;AF_NFE=7.26388e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|1|0|3|1|2|2|4|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-29;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.75899e-05;Hom=0;AF_POPMAX=9.84252e-05;AN_POPMAX=30480;AC_NFE=8;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|3|2|2|6|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=6.75017e-05;AF_AFR=0.00000e+00;AC_raw=15;AB_MEDIAN=4.19355e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=4.55506e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|13;Hom_raw=0;AF_SAS=9.84252e-05;AS_RF=9.10989e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=9.08540e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:0.0001008,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001161,AFR_MAF=T:0.0001995,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000258960.2:c.126C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=144,CDS_position=126,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766535198,VARIANT_CLASS=SNV,Protein_position=42,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:9.060e-05,HGVSc=ENST00000258960.2:c.126C>T,ExAC_Adj_MAF=T:9.878e-05
CDS|ENST00000258960	VCF	synonymous_variant	154	154	0.0	.	.	AC_Male=148;AF_NFE=1.34979e-03;Hom_FIN=0;GQ_MEDIAN=80;AB_HIST_ALT=0|0|4|13|34|85|90|44|24|6|1|2|0|0|1|0|0|0|0|0;AC_FIN=74;DREF_MEDIAN=1.00000e-08;AF_OTH=1.30939e-03;alleles=T%2CC;AF_FIN=3.42910e-03;AC_OTH=7;Hom_Male=0;AC=275;Hom_NFE=0;AF=1.14690e-03;Hom=0;AF_POPMAX=3.42910e-03;AN_POPMAX=21580;AC_NFE=145;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|5|4|20|31|38|39|37|27|29|22|24|7|6|3|2|2|0|1;AF_Male=1.12191e-03;AF_AFR=1.81476e-03;AC_raw=304;AB_MEDIAN=3.07692e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=1.23127e-03;DP_MEDIAN=42;AF_Female=1.17747e-03;GQ_HIST_ALT=4|4|6|8|5|9|8|12|6|14|13|6|13|13|19|10|18|17|12|107;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=5.26862e-02;Hom_AMR=0;AC_EAS=6;AC_Female=127;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.51206e-04;AC_SAS=0;POPMAX=FIN;AC_POPMAX=74;AC_AFR=27;Hom_SAS=0;AC_ASJ=12;AF_raw=1.24619e-03;Hom_Female=0;AF_AMR=1.20409e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:0.001857,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0.001923,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0.001052,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.141T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0.005814,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=2/12,ExAC_AMR_MAF=C:0.001447,cDNA_position=159,CDS_position=141,ExAC_NFE_MAF=C:0.01002,SYMBOL=NMT1,Existing_variation=rs777402320,VARIANT_CLASS=SNV,Protein_position=47,Codons=agT/agC,MINIMISED=1,ExAC_AFR_MAF=C:1.911e-03,HGVSc=ENST00000258960.2:c.141T>C,ExAC_Adj_MAF=C:0.000438
CDS|ENST00000258960	VCF	synonymous_variant	214	214	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|1|2|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.10793e-31;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.78394e-05;Hom=0;AF_POPMAX=3.99467e-04;AN_POPMAX=15020;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|1|2|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.68939e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.91379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=4.11794e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.74988e-01;Hom_AMR=0;AC_EAS=6;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.99467e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.46164e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:6.366e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=G:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,EAS_MAF=G:0,EUR_MAF=G:0.003,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.001103,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=G:0.0006,Amino_acids=K,HGVSp=ENST00000258960.2:c.201A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=2/12,ExAC_AMR_MAF=G:0,cDNA_position=219,CDS_position=201,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs141656657,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=67,AA_MAF=G:0,Codons=aaA/aaG,MINIMISED=1,ExAC_AFR_MAF=G:3.314e-05,HGVSc=ENST00000258960.2:c.201A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	217	217	0.0	.	.	AC_Male=0;AF_NFE=1.12471e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.76844e-06;Hom=0;AF_POPMAX=1.12471e-05;AN_POPMAX=88912;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.05753e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.93464e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10344e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.204C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=2/12,cDNA_position=222,CDS_position=204,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=68,Codons=ggC/ggT,MINIMISED=1,HGVSc=ENST00000258960.2:c.204C>T
CDS|ENST00000258960	VCF	synonymous_variant	223	223	0.0	.	.	AC_Male=6;AF_NFE=8.41548e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|2|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15518e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=3.50814e-05;Hom=0;AF_POPMAX=8.41548e-05;AN_POPMAX=83180;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|1|0|2|1|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=5.48296e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.21637e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.10980e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12023e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.28394e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:5.723e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001152,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000258960.2:c.210G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=2/12,ExAC_AMR_MAF=A:0,cDNA_position=228,CDS_position=210,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs369434915,VARIANT_CLASS=SNV,Protein_position=70,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:2.496e-05,HGVSc=ENST00000258960.2:c.210G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	235	235	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-83;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.48408e-06;Hom=0;AF_POPMAX=9.03506e-05;AN_POPMAX=11068;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=9.03506e-05;AC_raw=1;AB_MEDIAN=6.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.21150e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.96517e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.3e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=T:0.0002,Amino_acids=A,HGVSp=ENST00000258960.2:c.222C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=2/12,ExAC_AMR_MAF=T:0.0002112,cDNA_position=240,CDS_position=222,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs184508172,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=74,AA_MAF=T:0,Codons=gcC/gcT,MINIMISED=1,ExAC_AFR_MAF=T:8.398e-06,HGVSc=ENST00000258960.2:c.222C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	262	262	0.0	.	.	AC_Male=0;AF_NFE=9.11594e-06;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15014e-06;Hom=0;AF_POPMAX=9.11594e-06;AN_POPMAX=109698;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.77778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=9.19912e-06;GQ_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.62962e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.372e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.518e-05,AFR_MAF=C:0,SWISSPROT=P30419,EAS_MAF=C:0,EUR_MAF=C:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=C:0.0002,Amino_acids=S,HGVSp=ENST00000258960.2:c.249T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=3/12,ExAC_AMR_MAF=C:0,cDNA_position=267,CDS_position=249,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs200633656,SAS_MAF=C:0.001,VARIANT_CLASS=SNV,Protein_position=83,AA_MAF=C:0,Codons=tcT/tcC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.249T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	synonymous_variant	286	286	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|2|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22868e-05;Hom=0;AF_POPMAX=9.08045e-05;AN_POPMAX=33038;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46949e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=6.81818e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.81347e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.72461e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=9.08045e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000258960.2:c.273A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=3/12,cDNA_position=291,CDS_position=273,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=91,Codons=gaA/gaG,MINIMISED=1,HGVSc=ENST00000258960.2:c.273A>G
CDS|ENST00000258960	VCF	synonymous_variant	301	301	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-142;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07917e-06;Hom=0;AF_POPMAX=6.55996e-05;AN_POPMAX=15244;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=6.55996e-05;AC_raw=1;AB_MEDIAN=4.83146e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.02657e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.95139e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.272e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=C:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=I,HGVSp=ENST00000258960.2:c.288T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,EA_MAF=C:0.0002,Allele=C,IMPACT=LOW,EXON=3/12,ExAC_AMR_MAF=C:9.641e-05,cDNA_position=306,CDS_position=288,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs372318247,VARIANT_CLASS=SNV,Protein_position=96,Codons=atT/atC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.288T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	synonymous_variant	307	307	0.0	.	.	AC_Male=1;AF_NFE=8.97747e-06;Hom_FIN=0;GQ_MEDIAN=73;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97611e-06;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14538e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.54779e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.00868e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.44770e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.266e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.294G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/12,ExAC_AMR_MAF=T:0,cDNA_position=312,CDS_position=294,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754577624,VARIANT_CLASS=SNV,Protein_position=98,Codons=ctG/ctT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.294G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	313	313	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07193e-06;Hom=0;AF_POPMAX=3.25457e-05;AN_POPMAX=30726;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43141e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25457e-05;AS_RF=8.52320e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.300A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=3/12,cDNA_position=318,CDS_position=300,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=100,Codons=tcA/tcG,MINIMISED=1,HGVSc=ENST00000258960.2:c.300A>G
CDS|ENST00000258960	VCF	synonymous_variant	325	325	0.0	.	.	AC_Male=1;AF_NFE=8.99006e-06;Hom_FIN=0;GQ_MEDIAN=34;AB_HIST_ALT=0|0|0|0|4|3|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=4.08532e-04;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=1.35404e-04;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44760e-05;Hom=0;AF_POPMAX=1.35404e-04;AN_POPMAX=22156;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.44114e-06;AF_AFR=1.31406e-04;AC_raw=8;AB_MEDIAN=2.47642e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=4.51467e-05;GQ_HIST_ALT=0|1|1|0|0|1|1|1|0|0|1|0|1|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.54316e-03;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:6.621e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:6.02e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.312A>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=3/12,ExAC_AMR_MAF=C:0.0002899,cDNA_position=330,CDS_position=312,ExAC_NFE_MAF=C:0.0001537,SYMBOL=NMT1,Existing_variation=rs746348189,VARIANT_CLASS=SNV,Protein_position=104,Codons=ggA/ggC,MINIMISED=1,ExAC_AFR_MAF=C:9.060e-05,HGVSc=ENST00000258960.2:c.312A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	synonymous_variant	331	331	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07701e-06;Hom=0;AF_POPMAX=3.25945e-05;AN_POPMAX=30680;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25945e-05;AS_RF=8.53172e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000258960.2:c.318C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/12,cDNA_position=336,CDS_position=318,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=106,Codons=gcC/gcT,MINIMISED=1,HGVSc=ENST00000258960.2:c.318C>T
CDS|ENST00000258960	VCF	synonymous_variant	349	349	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-42;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07501e-06;Hom=0;AF_POPMAX=2.99419e-05;AN_POPMAX=33398;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43450e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.92593e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.81783e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99419e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000258960.2:c.336T>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=3/12,cDNA_position=354,CDS_position=336,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=112,Codons=gcT/gcC,MINIMISED=1,HGVSc=ENST00000258960.2:c.336T>C
CDS|ENST00000258960	VCF	synonymous_variant	352	352	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07465e-06;Hom=0;AF_POPMAX=2.99455e-05;AN_POPMAX=33394;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.67568e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=37;AF_Female=9.01518e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92008e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99455e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.339C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/12,cDNA_position=357,CDS_position=339,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=113,Codons=agC/agT,MINIMISED=1,HGVSc=ENST00000258960.2:c.339C>T
CDS|ENST00000258960	VCF	synonymous_variant	370	370	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=25;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15231e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=8;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66799e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000258960.2:c.357C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/12,cDNA_position=375,CDS_position=357,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=119,Codons=ttC/ttT,MINIMISED=1,HGVSc=ENST00000258960.2:c.357C>T
CDS|ENST00000258960	VCF	synonymous_variant	379	379	0.0	.	.	AC_Male=0;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-30;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.78261e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=9.08364e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.39564e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.366G>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/12,cDNA_position=384,CDS_position=366,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=122,Codons=acG/acT,HGVSc=ENST00000258960.2:c.366G>T
CDS|ENST00000258960	VCF	synonymous_variant	379	379	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|1|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.69441e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=3.02810e-05;AN_POPMAX=33024;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|3|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48671e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=1.60256e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.95538e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=3.02810e-05;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.366G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=3/12,cDNA_position=384,CDS_position=366,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=122,Codons=acG/acA,HGVSc=ENST00000258960.2:c.366G>A
CDS|ENST00000258960	VCF	synonymous_variant	385	385	0.0	.	.	AC_Male=13;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|2|0|5|2|0|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=15;Hom_NFE=0;AF=6.19001e-05;Hom=0;AF_POPMAX=4.28788e-04;AN_POPMAX=30318;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|4|2|1|1|1|0|1|0|0|2|1|0|0|1|0|0;AF_Male=9.78076e-05;AF_AFR=6.60153e-05;AC_raw=15;AB_MEDIAN=4.72797e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.82795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|15;Hom_raw=0;AF_SAS=4.28788e-04;AS_RF=9.33794e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.89692e-05;AC_SAS=13;POPMAX=SAS;AC_POPMAX=13;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09088e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.385e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0005311,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.372C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=3/12,ExAC_AMR_MAF=T:9.632e-05,cDNA_position=390,CDS_position=372,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs774578466,VARIANT_CLASS=SNV,Protein_position=124,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-05,HGVSc=ENST00000258960.2:c.372C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	391	391	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-31;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13839e-06;Hom=0;AF_POPMAX=3.31279e-05;AN_POPMAX=30186;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.54523e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.58333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.31279e-05;AS_RF=8.33412e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.422e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.378C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=3/12,ExAC_AMR_MAF=G:0,cDNA_position=396,CDS_position=378,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767261647,VARIANT_CLASS=SNV,Protein_position=126,Codons=ccC/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.378C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	412	412	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06669e-06;Hom=0;AF_POPMAX=3.24971e-05;AN_POPMAX=30772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42501e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24971e-05;AS_RF=9.28048e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.289e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000258960.2:c.399C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=T:0,cDNA_position=417,CDS_position=399,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs760391896,VARIANT_CLASS=SNV,Protein_position=133,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000258960.2:c.399C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	415	415	0.0	.	.	AC_Male=1;AF_NFE=8.97054e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-32;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06544e-06;Hom=0;AF_POPMAX=8.97054e-06;AN_POPMAX=111476;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.48276e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.93308e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.285e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.508e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.402C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=A:0,cDNA_position=420,CDS_position=402,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs766241230,VARIANT_CLASS=SNV,Protein_position=134,Codons=acC/acA,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000258960.2:c.402C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	421	421	0.0	.	.	AC_Male=0;AF_NFE=8.97022e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-93;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06521e-06;Hom=0;AF_POPMAX=8.97022e-06;AN_POPMAX=111480;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.90164e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98779e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40909e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.408C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/12,cDNA_position=426,CDS_position=408,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=136,Codons=ggC/ggT,MINIMISED=1,HGVSc=ENST00000258960.2:c.408C>T
CDS|ENST00000258960	VCF	synonymous_variant	424	424	0.0	.	.	AC_Male=22;AF_NFE=2.68986e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|9|6|8|6|4|1|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.00000e-61;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=37;Hom_NFE=0;AF=1.50378e-04;Hom=0;AF_POPMAX=2.68986e-04;AN_POPMAX=111530;AC_NFE=30;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|6|3|4|4|5|5|3|2|0|2|3|0|0|0|0;AF_Male=1.63236e-04;AF_AFR=0.00000e+00;AC_raw=37;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=0.00000e+00;DP_MEDIAN=45;AF_Female=1.34805e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|37;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=30;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.50240e-04;Hom_Female=0;AF_AMR=1.78710e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0003,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.411C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,EA_MAF=G:0.0002,Allele=G,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=429,CDS_position=411,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,Protein_position=137,Codons=ccC/ccG,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000258960.2:c.411C>G,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000258960	VCF	synonymous_variant	424	424	0.0	.	.	AC_Male=4;AF_NFE=2.68986e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|3|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-59;AF_OTH=3.64830e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25142e-05;Hom=0;AF_POPMAX=1.30702e-04;AN_POPMAX=15302;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|1|1|2|2|0|0|0|0|0|0|0|0|0;AF_Male=2.96793e-05;AF_AFR=1.30702e-04;AC_raw=8;AB_MEDIAN=4.75384e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.59479e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=2;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0003,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.411C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,EA_MAF=G:0.0002,Allele=T,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=429,CDS_position=411,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,Protein_position=137,Codons=ccC/ccT,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000258960.2:c.411C>T,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000258960	VCF	synonymous_variant	436	436	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06329e-06;Hom=0;AF_POPMAX=5.79845e-05;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53191e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50090e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79845e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.261e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0,EUR_MAF=T:0.001,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001157,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=T:0.0002,Amino_acids=D,HGVSp=ENST00000258960.2:c.423C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=T:0,cDNA_position=441,CDS_position=423,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs535242567,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=141,AA_MAF=T:0,Codons=gaC/gaT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.423C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	439	439	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-50;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06339e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41851e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43104e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=K,HGVSp=ENST00000258960.2:c.426G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=4/12,cDNA_position=444,CDS_position=426,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=142,Codons=aaG/aaA,MINIMISED=1,HGVSc=ENST00000258960.2:c.426G>A
CDS|ENST00000258960	VCF	synonymous_variant	484	484	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|0|1|2|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-64;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84465e-05;Hom=0;AF_POPMAX=2.08445e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|0|1|0|2|0|1|0|0|1|0|0;AF_Male=1.48372e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=7;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=4.49317e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84239e-05;Hom_Female=0;AF_AMR=2.08445e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.65e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.471C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=G:0,cDNA_position=489,CDS_position=471,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs559376009,VARIANT_CLASS=SNV,Protein_position=157,Codons=acC/acG,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.471C>G,ExAC_Adj_MAF=G:0.0001732
CDS|ENST00000258960	VCF	synonymous_variant	500	500	0.0	.	.	AC_Male=25006;AF_NFE=2.09922e-01;Hom_FIN=285;GQ_MEDIAN=99;AB_HIST_ALT=0|0|5|15|72|453|1543|3857|7281|7755|7846|3986|1826|582|145|27|12|4|3|0;AC_FIN=3550;DREF_MEDIAN=1.00000e-73;AF_OTH=1.77555e-01;alleles=C%2CT;AF_FIN=1.59379e-01;AC_OTH=973;Hom_Male=2665;AC=45042;Hom_NFE=2465;AF=1.83181e-01;Hom=4839;AF_POPMAX=3.36036e-01;AN_POPMAX=15296;AC_NFE=23384;AS_FilterStatus=PASS;Hom_OTH=97;DP_HIST_ALT=2|26|94|195|538|1305|2559|3767|4480|4660|4316|3950|3356|2703|2157|1571|1256|914|624|548;AF_Male=1.85675e-01;AF_AFR=3.36036e-01;AC_raw=45128;AB_MEDIAN=4.75610e-01;Hom_EAS=11;AC_AMR=2943;AF_ASJ=1.65819e-01;DP_MEDIAN=52;AF_Female=1.80160e-01;GQ_HIST_ALT=6|6|7|9|6|14|13|17|10|21|33|20|43|66|53|88|83|83|130|39562;Hom_raw=4858;AF_SAS=2.21782e-01;AS_RF=9.54732e-01;Hom_AMR=167;AC_EAS=595;AC_Female=20036;Hom_AFR=875;Hom_ASJ=130;AF_EAS=3.44968e-02;AC_SAS=6826;POPMAX=AFR;AC_POPMAX=5140;AC_AFR=5140;Hom_SAS=809;AC_ASJ=1631;AF_raw=1.83246e-01;Hom_Female=2174;AF_AMR=8.76362e-02;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:0.1935,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.2031,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0.3616,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.2069,AFR_MAF=T:0.2226,SWISSPROT=P30419,EAS_MAF=T:0.134,EUR_MAF=T:0.0367,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0346,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=T:0.1991,Amino_acids=L,HGVSp=ENST00000258960.2:c.487C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0.1752,CCDS=CCDS11494.1,EA_MAF=T:0.325,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=T:0.3348,cDNA_position=505,CDS_position=487,ExAC_NFE_MAF=T:0.1553,SYMBOL=NMT1,Existing_variation=rs1132898&COSM3755586,SAS_MAF=T:0.1769,VARIANT_CLASS=SNV,Protein_position=163,AA_MAF=T:0.2157,Codons=Ctg/Ttg,MINIMISED=1,ExAC_AFR_MAF=T:0.193,HGVSc=ENST00000258960.2:c.487C>T,ExAC_Adj_MAF=T:0.08946
CDS|ENST00000258960	VCF	synonymous_variant	502	502	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-69;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06557e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.42280e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.31034e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=8.87045e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.489G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=4/12,cDNA_position=507,CDS_position=489,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=163,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000258960.2:c.489G>A
CDS|ENST00000258960	VCF	synonymous_variant	505	505	0.0	.	.	AC_Male=2;AF_NFE=1.79498e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|2|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-46;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21991e-05;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|1;AF_Male=1.48469e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.69796e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=8.99184e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.10458e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.652e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.006e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.492C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=T:0,cDNA_position=510,CDS_position=492,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749766632,VARIANT_CLASS=SNV,Protein_position=164,Codons=ggC/ggT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.492C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	511	511	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-64;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06901e-06;Hom=0;AF_POPMAX=6.53595e-05;AN_POPMAX=15300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53595e-05;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=8.99653e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.86417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000258960.2:c.498T>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=4/12,cDNA_position=516,CDS_position=498,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=166,Codons=cgT/cgG,MINIMISED=1,HGVSc=ENST00000258960.2:c.498T>G
CDS|ENST00000258960	VCF	synonymous_variant	514	514	0.0	.	.	AC_Male=0;AF_NFE=8.98537e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-29;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06891e-06;Hom=0;AF_POPMAX=8.98537e-06;AN_POPMAX=111292;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.11111e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=18;AF_Female=8.99491e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.57047e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.267e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.503e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.501T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=C:0,cDNA_position=519,CDS_position=501,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs772281237,VARIANT_CLASS=SNV,Protein_position=167,Codons=ggT/ggC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.501T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	synonymous_variant	535	535	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|2|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16108e-109;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.24865e-05;Hom=0;AF_POPMAX=2.38223e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|3|0|0|0|0|0|1|1;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.25397e-01;Hom_EAS=0;AC_AMR=8;AF_ASJ=0.00000e+00;DP_MEDIAN=93;AF_Female=5.38812e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=6;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=8;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=2.38223e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:3.295e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.522C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/12,ExAC_AMR_MAF=T:0,cDNA_position=540,CDS_position=522,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs770678984,VARIANT_CLASS=SNV,Protein_position=174,Codons=acC/acT,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000258960.2:c.522C>T,ExAC_Adj_MAF=T:0.0003455
CDS|ENST00000258960	VCF	synonymous_variant	568	568	0.0	.	.	AC_Male=4;AF_NFE=5.37095e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-123;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43643e-05;Hom=0;AF_POPMAX=5.37095e-05;AN_POPMAX=111712;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|1;AF_Male=2.96512e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.30292e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=135;AF_Female=1.79598e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.942e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.991e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000258960.2:c.555C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/12,ExAC_AMR_MAF=T:0,cDNA_position=573,CDS_position=555,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs776474941,VARIANT_CLASS=SNV,Protein_position=185,Codons=gaC/gaT,MINIMISED=1,ExAC_AFR_MAF=T:4.942e-05,HGVSc=ENST00000258960.2:c.555C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	571	571	0.0	.	.	AC_Male=0;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-101;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.05660e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=106;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12871e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000258960.2:c.558C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=5/12,cDNA_position=576,CDS_position=558,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=186,Codons=aaC/aaT,MINIMISED=1,HGVSc=ENST00000258960.2:c.558C>T
CDS|ENST00000258960	VCF	synonymous_variant	583	583	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-132;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.34426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=122;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.50786e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000258960.2:c.570T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=5/12,ExAC_AMR_MAF=C:0,cDNA_position=588,CDS_position=570,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs759459614,VARIANT_CLASS=SNV,Protein_position=190,Codons=ttT/ttC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.570T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	synonymous_variant	592	592	0.0	.	.	AC_Male=4;AF_NFE=1.16371e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|3|5|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-93;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=13;Hom_NFE=0;AF=5.27897e-05;Hom=0;AF_POPMAX=1.16371e-04;AN_POPMAX=111712;AC_NFE=13;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|2|1|1|0|0|1|0|0|1;AF_Male=2.96507e-05;AF_AFR=0.00000e+00;AC_raw=13;AB_MEDIAN=4.05405e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=97;AF_Female=8.08219e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|13;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.28067e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=13;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.27872e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:6.589e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001199,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.579C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=5/12,ExAC_AMR_MAF=A:0,cDNA_position=597,CDS_position=579,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs372926712,VARIANT_CLASS=SNV,Protein_position=193,Codons=tcC/tcA,MINIMISED=1,ExAC_AFR_MAF=A:6.589e-05,HGVSc=ENST00000258960.2:c.579C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	595	595	0.0	.	.	AC_Male=380;AF_NFE=2.32750e-03;Hom_FIN=3;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|2|40|88|203|202|119|49|4|0|0|0|0|0|0|0;AC_FIN=293;DREF_MEDIAN=5.01187e-117;AF_OTH=3.83072e-03;alleles=G%2CA;AF_FIN=1.31390e-02;AC_OTH=21;Hom_Male=2;AC=716;Hom_NFE=0;AF=2.90754e-03;Hom=4;AF_POPMAX=1.31390e-02;AN_POPMAX=22300;AC_NFE=260;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|5|6|15|17|25|30|39|50|52|47|44|38|56;AF_Male=2.81686e-03;AF_AFR=2.61370e-04;AC_raw=716;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=45;AF_ASJ=9.23858e-03;DP_MEDIAN=93;AF_Female=3.01740e-03;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|712;Hom_raw=4;AF_SAS=3.24865e-05;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=1;AC_Female=336;Hom_AFR=0;Hom_ASJ=1;AF_EAS=5.79777e-05;AC_SAS=1;POPMAX=FIN;AC_POPMAX=293;AC_AFR=4;Hom_SAS=0;AC_ASJ=91;AF_raw=2.90735e-03;Hom_Female=2;AF_AMR=1.34000e-03;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.002586,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0022,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=A:0.0004,Amino_acids=P,HGVSp=ENST00000258960.2:c.582G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0.003311,CCDS=CCDS11494.1,EA_MAF=A:0.0005,Allele=A,IMPACT=LOW,EXON=5/12,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=600,CDS_position=582,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,Protein_position=194,AA_MAF=A:0,Codons=ccG/ccA,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000258960.2:c.582G>A,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000258960	VCF	synonymous_variant	595	595	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-124;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.71429e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41835e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.002586,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0022,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=A:0.0004,Amino_acids=P,HGVSp=ENST00000258960.2:c.582G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0.003311,CCDS=CCDS11494.1,EA_MAF=A:0.0005,Allele=T,IMPACT=LOW,EXON=5/12,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=600,CDS_position=582,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,Protein_position=194,AA_MAF=A:0,Codons=ccG/ccT,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000258960.2:c.582G>T,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000258960	VCF	synonymous_variant	625	625	0.0	.	.	AC_Male=4;AF_NFE=5.37577e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00079e-202;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43754e-05;Hom=0;AF_POPMAX=5.37577e-05;AN_POPMAX=111612;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|1;AF_Male=2.96630e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=5.20944e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=152;AF_Female=1.79691e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35748e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.612C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=6/12,ExAC_AMR_MAF=T:0,cDNA_position=630,CDS_position=612,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757227703&COSM4130155,VARIANT_CLASS=SNV,Protein_position=204,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000258960.2:c.612C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	652	652	0.0	.	.	AC_Male=1;AF_NFE=1.79045e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-65;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12163e-06;Hom=0;AF_POPMAX=1.79045e-05;AN_POPMAX=111704;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.08500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=57;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.42948e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.639G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=6/12,ExAC_AMR_MAF=A:0,cDNA_position=657,CDS_position=639,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768715452,VARIANT_CLASS=SNV,Protein_position=213,Codons=ggG/ggA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.639G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	664	664	0.0	.	.	AC_Male=9;AF_NFE=2.32741e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|11|10|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-104;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=26;Hom_NFE=0;AF=1.05578e-04;Hom=0;AF_POPMAX=2.32741e-04;AN_POPMAX=111712;AC_NFE=26;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|3|0|2|5|0|2;AF_Male=6.67141e-05;AF_AFR=0.00000e+00;AC_raw=26;AB_MEDIAN=4.45780e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=98;AF_Female=1.52658e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|26;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=17;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=26;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.05574e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.885e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0003,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001798,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000258960.2:c.651C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=6/12,ExAC_AMR_MAF=T:0,cDNA_position=669,CDS_position=651,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs199671891,VARIANT_CLASS=SNV,Protein_position=217,Codons=gtC/gtT,MINIMISED=1,ExAC_AFR_MAF=T:9.884e-05,HGVSc=ENST00000258960.2:c.651C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	673	673	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-154;AF_OTH=1.82282e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.60938e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000258960.2:c.660G>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=6/12,cDNA_position=678,CDS_position=660,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=220,Codons=cgG/cgC,MINIMISED=1,HGVSc=ENST00000258960.2:c.660G>C
CDS|ENST00000258960	VCF	synonymous_variant	694	694	0.0	.	.	AC_Male=2;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21823e-05;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=1.48249e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.91803e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.01565e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.647e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.681C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=6/12,ExAC_AMR_MAF=T:0,cDNA_position=699,CDS_position=681,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772957252,VARIANT_CLASS=SNV,Protein_position=227,Codons=agC/agT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.681C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	703	703	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-140;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.49153e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=118;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.690A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=6/12,ExAC_AMR_MAF=G:0,cDNA_position=708,CDS_position=690,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs770200317,VARIANT_CLASS=SNV,Protein_position=230,Codons=ccA/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.690A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	721	721	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-84;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06138e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.92754e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=69;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.86417e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=Y,HGVSp=ENST00000258960.2:c.708T>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=6/12,cDNA_position=726,CDS_position=708,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=236,Codons=taT/taC,MINIMISED=1,HGVSc=ENST00000258960.2:c.708T>C
CDS|ENST00000258960	VCF	synonymous_variant	775	775	0.0	.	.	AC_Male=1;AF_NFE=8.95367e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-83;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06121e-06;Hom=0;AF_POPMAX=8.95367e-06;AN_POPMAX=111686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41400e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.37037e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.49406e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.762G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=7/12,cDNA_position=780,CDS_position=762,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=254,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000258960.2:c.762G>A
CDS|ENST00000258960	VCF	synonymous_variant	781	781	0.0	.	.	AC_Male=2;AF_NFE=2.68562e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-156;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21825e-05;Hom=0;AF_POPMAX=2.68562e-05;AN_POPMAX=111706;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0;AF_Male=1.48265e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.28302e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33696e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.768C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=T:0,cDNA_position=786,CDS_position=768,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs770379933,VARIANT_CLASS=SNV,Protein_position=256,Codons=tcC/tcT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.768C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	787	787	0.0	.	.	AC_Male=7;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|3|5|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-120;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.46675e-05;Hom=0;AF_POPMAX=3.24865e-04;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|2|1|2|0|0|0|0|1|1;AF_Male=5.18880e-05;AF_AFR=6.53424e-05;AC_raw=11;AB_MEDIAN=4.69613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=92;AF_Female=3.59202e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=3.24865e-04;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=10;POPMAX=SAS;AC_POPMAX=10;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:5.766e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0003634,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000258960.2:c.774G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=792,CDS_position=774,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs780855060,VARIANT_CLASS=SNV,Protein_position=258,Codons=agG/agA,MINIMISED=1,ExAC_AFR_MAF=A:5.765e-05,HGVSc=ENST00000258960.2:c.774G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	811	811	0.0	.	.	AC_Male=23;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|8|24|20|21|5|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.07688e-127;AF_OTH=1.82349e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=85;Hom_NFE=0;AF=3.45164e-04;Hom=1;AF_POPMAX=3.98589e-03;AN_POPMAX=15304;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|2|4|1|6|4|3|5|6|3|1|3|5;AF_Male=1.70492e-04;AF_AFR=3.98589e-03;AC_raw=85;AB_MEDIAN=4.72222e-01;Hom_EAS=0;AC_AMR=19;AF_ASJ=3.04569e-04;DP_MEDIAN=97;AF_Female=5.56773e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|84;Hom_raw=1;AF_SAS=3.24865e-05;AS_RF=9.53297e-01;Hom_AMR=0;AC_EAS=0;AC_Female=62;Hom_AFR=1;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=61;AC_AFR=61;Hom_SAS=0;AC_ASJ=3;AF_raw=3.45147e-04;Hom_Female=1;AF_AMR=5.65779e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.0004366,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0002,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0.0061,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=A:0.0016,Amino_acids=E,HGVSp=ENST00000258960.2:c.798G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0.001101,CCDS=CCDS11494.1,EA_MAF=A:0.0052,Allele=A,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=A:0.004228,cDNA_position=816,CDS_position=798,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs146578323,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=266,AA_MAF=A:0,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:4.365e-04,HGVSc=ENST00000258960.2:c.798G>A,ExAC_Adj_MAF=A:0.0005183
CDS|ENST00000258960	VCF	synonymous_variant	817	817	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-30;AF_OTH=1.82349e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=8.98037e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.72787e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.804C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=7/12,cDNA_position=822,CDS_position=804,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=268,Codons=acC/acT,MINIMISED=1,HGVSc=ENST00000258960.2:c.804C>T
CDS|ENST00000258960	VCF	synonymous_variant	832	832	0.0	.	.	AC_Male=15;AF_NFE=3.58153e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|5|5|3|5|3|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-69;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=25;Hom_NFE=0;AF=1.01531e-04;Hom=0;AF_POPMAX=1.11082e-03;AN_POPMAX=15304;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|1|1|2|4|5|1|1|1|2|0|1|0;AF_Male=1.11200e-04;AF_AFR=1.11082e-03;AC_raw=25;AB_MEDIAN=4.82014e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98166e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|25;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.93009e-01;Hom_AMR=0;AC_EAS=0;AC_Female=10;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=17;AC_AFR=17;Hom_SAS=0;AC_ASJ=0;AF_raw=1.01514e-04;Hom_Female=0;AF_AMR=1.19111e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:4.943e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=A:0.0002,Amino_acids=L,HGVSp=ENST00000258960.2:c.819G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0005,Allele=A,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=A:0.0003844,cDNA_position=837,CDS_position=819,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs201216212,SAS_MAF=A:0.001,VARIANT_CLASS=SNV,Protein_position=273,AA_MAF=A:0,Codons=ctG/ctA,MINIMISED=1,ExAC_AFR_MAF=A:4.942e-05,HGVSc=ENST00000258960.2:c.819G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	844	844	0.0	.	.	AC_Male=1;AF_NFE=8.95383e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-154;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06128e-06;Hom=0;AF_POPMAX=8.95383e-06;AN_POPMAX=111684;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41345e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=115;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000258960.2:c.831C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=T:0,cDNA_position=849,CDS_position=831,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766086965,VARIANT_CLASS=SNV,Protein_position=277,Codons=ttC/ttT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.831C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	862	862	0.0	.	.	AC_Male=3;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|1|1|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-112;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43815e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|1|2|0|1;AF_Male=2.22499e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.63415e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=87;AF_Female=2.69648e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=4;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=1;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.24e-06&T:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0003467,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000258960.2:c.849C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=A:0&T:0,cDNA_position=867,CDS_position=849,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs773804544,VARIANT_CLASS=SNV,Protein_position=283,Codons=gcC/gcT,ExAC_AFR_MAF=A:8.236e-06&T:3.295e-05,HGVSc=ENST00000258960.2:c.849C>T,ExAC_Adj_MAF=A:0&T:0
CDS|ENST00000258960	VCF	synonymous_variant	862	862	0.0	.	.	AC_Male=1;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-101;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06359e-06;Hom=0;AF_POPMAX=8.96379e-06;AN_POPMAX=111560;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.41664e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=84;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.24e-06&T:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0003467,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000258960.2:c.849C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=A:0&T:0,cDNA_position=867,CDS_position=849,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs773804544,VARIANT_CLASS=SNV,Protein_position=283,Codons=gcC/gcA,ExAC_AFR_MAF=A:8.236e-06&T:3.295e-05,HGVSc=ENST00000258960.2:c.849C>A,ExAC_Adj_MAF=A:0&T:0
CDS|ENST00000258960	VCF	synonymous_variant	865	865	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-131;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06342e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41675e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.35644e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=101;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.45417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.241e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.852G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=T:0,cDNA_position=870,CDS_position=852,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs777042262,VARIANT_CLASS=SNV,Protein_position=284,Codons=ggG/ggT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.852G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	874	874	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|2|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38770e-91;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03277e-05;Hom=0;AF_POPMAX=2.89922e-04;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|1|0|1|1|1|0|0;AF_Male=2.22605e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.67647e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=1.79853e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43239e-01;Hom_AMR=0;AC_EAS=5;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.89922e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:3.298e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.0004622,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.861A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=G:0,cDNA_position=879,CDS_position=861,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs765144876,VARIANT_CLASS=SNV,Protein_position=287,Codons=ctA/ctG,MINIMISED=1,ExAC_AFR_MAF=G:3.295e-05,HGVSc=ENST00000258960.2:c.861A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	877	877	0.0	.	.	AC_Male=1;AF_NFE=8.97876e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-116;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06693e-06;Hom=0;AF_POPMAX=8.97876e-06;AN_POPMAX=111374;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.42269e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.18519e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=81;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.07420e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=1,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.864A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,SOMATIC=1,Allele=G,IMPACT=LOW,EXON=7/12,cDNA_position=882,CDS_position=864,SYMBOL=NMT1,Existing_variation=COSM980092,VARIANT_CLASS=SNV,Protein_position=288,Codons=ccA/ccG,MINIMISED=1,HGVSc=ENST00000258960.2:c.864A>G
CDS|ENST00000258960	VCF	synonymous_variant	883	883	0.0	.	.	AC_Male=16886;AF_NFE=7.81798e-02;Hom_FIN=144;GQ_MEDIAN=99;AB_HIST_ALT=0|0|4|11|34|169|815|2369|5579|6526|6364|2859|1315|395|126|40|13|6|2|0;AC_FIN=2671;DREF_MEDIAN=1.58489e-82;AF_OTH=1.21898e-01;alleles=C%2CT;AF_FIN=1.19862e-01;AC_OTH=668;Hom_Male=1379;AC=32227;Hom_NFE=374;AF=1.31220e-01;Hom=2825;AF_POPMAX=2.70280e-01;AN_POPMAX=17234;AC_NFE=8690;AS_FilterStatus=PASS;Hom_OTH=38;DP_HIST_ALT=0|34|152|543|1210|1834|1980|1919|2086|2037|2144|2084|2059|2011|1891|1563|1322|1089|843|766;AF_Male=1.25481e-01;AF_AFR=1.64684e-01;AC_raw=32293;AB_MEDIAN=4.80000e-01;Hom_EAS=624;AC_AMR=8200;AF_ASJ=1.11156e-01;DP_MEDIAN=56;AF_Female=1.38175e-01;GQ_HIST_ALT=2|5|5|5|6|4|15|8|13|29|37|35|59|87|46|89|130|54|99|28732;Hom_raw=2833;AF_SAS=1.21133e-01;AS_RF=9.54732e-01;Hom_AMR=1132;AC_EAS=4658;AC_Female=15341;Hom_AFR=203;Hom_ASJ=67;AF_EAS=2.70280e-01;AC_SAS=3728;POPMAX=EAS;AC_POPMAX=4658;AC_AFR=2520;Hom_SAS=243;AC_ASJ=1092;AF_raw=1.31127e-01;Hom_Female=1446;AF_AMR=2.44470e-01;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:0.1255,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.084,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0.1717,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.08058,AFR_MAF=T:0.1247,SWISSPROT=P30419,EAS_MAF=T:0.2003,EUR_MAF=T:0.2669,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.2664,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=T:0.1707,Amino_acids=P,HGVSp=ENST00000258960.2:c.870C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0.1082,CCDS=CCDS11494.1,EA_MAF=T:0.1609,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=T:0.1637,cDNA_position=888,CDS_position=870,ExAC_NFE_MAF=T:0.1181,SYMBOL=NMT1,Existing_variation=rs2239922&COSM4130156,SAS_MAF=T:0.0845,VARIANT_CLASS=SNV,Protein_position=290,AA_MAF=T:0.138,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:0.125,HGVSc=ENST00000258960.2:c.870C>T,ExAC_Adj_MAF=T:0.2522
CDS|ENST00000258960	VCF	synonymous_variant	892	892	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-66;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07485e-06;Hom=0;AF_POPMAX=3.24971e-05;AN_POPMAX=30772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43837e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24971e-05;AS_RF=9.36271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.879C>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=7/12,cDNA_position=897,CDS_position=879,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=293,Codons=acC/acG,MINIMISED=1,HGVSc=ENST00000258960.2:c.879C>G
CDS|ENST00000258960	VCF	synonymous_variant	929	929	0.0	.	.	AC_Male=35456;AF_NFE=2.86445e-01;Hom_FIN=602;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|5|45|265|1612|6264|14024|13853|7316|1836|403|56|20|5|1|7|0|0;AC_FIN=5122;DREF_MEDIAN=5.01187e-129;AF_OTH=2.67688e-01;alleles=C%2CT;AF_FIN=2.29686e-01;AC_OTH=1468;Hom_Male=4900;AC=62473;Hom_NFE=4541;AF=2.53714e-01;Hom=8385;AF_POPMAX=3.13873e-01;AN_POPMAX=30780;AC_NFE=31993;AS_FilterStatus=PASS;Hom_OTH=200;DP_HIST_ALT=0|4|10|40|98|183|365|643|1031|1413|1780|2104|2153|2372|2313|2427|2475|2656|2744|3260;AF_Male=2.62863e-01;AF_AFR=8.24621e-02;AC_raw=62491;AB_MEDIAN=4.51613e-01;Hom_EAS=523;AC_AMR=5860;AF_ASJ=2.83046e-01;DP_MEDIAN=99;AF_Female=2.42631e-01;GQ_HIST_ALT=1|1|1|3|5|1|2|2|7|5|3|7|10|13|9|10|20|17|27|53958;Hom_raw=8389;AF_SAS=3.13873e-01;AS_RF=9.54732e-01;Hom_AMR=536;AC_EAS=4319;AC_Female=27017;Hom_AFR=44;Hom_ASJ=372;AF_EAS=2.50435e-01;AC_SAS=9661;POPMAX=SAS;AC_POPMAX=9661;AC_AFR=1262;Hom_SAS=1567;AC_ASJ=2788;AF_raw=2.53748e-01;Hom_Female=3485;AF_AMR=1.74509e-01;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:0.2516,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.2892,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0.059,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.2796,AFR_MAF=T:0.3133,SWISSPROT=P30419,EAS_MAF=T:0.2017,EUR_MAF=T:0.2748,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.2472,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=T:0.2240,Amino_acids=L,HGVSp=ENST00000258960.2:c.916C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0.2671,CCDS=CCDS11494.1,EA_MAF=T:0.0921,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=8/12,ExAC_AMR_MAF=T:0.08428,cDNA_position=934,CDS_position=916,ExAC_NFE_MAF=T:0.2272,SYMBOL=NMT1,Existing_variation=rs2239923&COSM4000177,SAS_MAF=T:0.2992,VARIANT_CLASS=SNV,Protein_position=306,AA_MAF=T:0.3333,Codons=Ctg/Ttg,MINIMISED=1,ExAC_AFR_MAF=T:0.252,HGVSc=ENST00000258960.2:c.916C>T,ExAC_Adj_MAF=T:0.1691
CDS|ENST00000258960	VCF	synonymous_variant	934	934	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-115;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57447e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.07652e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=I,HGVSp=ENST00000258960.2:c.921T>C(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=8/12,cDNA_position=939,CDS_position=921,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=307,Codons=atT/atC,MINIMISED=1,HGVSc=ENST00000258960.2:c.921T>C
CDS|ENST00000258960	VCF	synonymous_variant	940	940	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-265;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.84211e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=190;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.26718e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000258960.2:c.927G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=8/12,ExAC_AMR_MAF=T:0,cDNA_position=945,CDS_position=927,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs779600514,VARIANT_CLASS=SNV,Protein_position=309,Codons=gtG/gtT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.927G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	946	946	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-52;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.25532e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.45417e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000258960.2:c.933C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=8/12,cDNA_position=951,CDS_position=933,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=311,Codons=ttC/ttT,MINIMISED=1,HGVSc=ENST00000258960.2:c.933C>T
CDS|ENST00000258960	VCF	synonymous_variant	955	955	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-21;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.56863e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=102;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=4.74649e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.942G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=8/12,cDNA_position=960,CDS_position=942,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=314,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000258960.2:c.942G>A
CDS|ENST00000258960	VCF	synonymous_variant	991	991	0.0	.	.	AC_Male=1;AF_NFE=8.96106e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-92;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06303e-06;Hom=0;AF_POPMAX=8.96106e-06;AN_POPMAX=111594;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41719e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.39683e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50841e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.978C>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=8/12,cDNA_position=996,CDS_position=978,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=326,Codons=ctC/ctG,MINIMISED=1,HGVSc=ENST00000258960.2:c.978C>G
CDS|ENST00000258960	VCF	synonymous_variant	997	997	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-120;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06375e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=104;AF_Female=8.98666e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20293e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.244e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000258960.2:c.984A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=8/12,ExAC_AMR_MAF=G:0,cDNA_position=1002,CDS_position=984,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs748936607,VARIANT_CLASS=SNV,Protein_position=328,Codons=cgA/cgG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.984A>G,ExAC_Adj_MAF=G:8.645e-05
CDS|ENST00000258960	VCF	synonymous_variant	1027	1027	0.0	.	.	AC_Male=1;AF_NFE=8.96636e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06560e-06;Hom=0;AF_POPMAX=8.96636e-06;AN_POPMAX=111528;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42236e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.05405e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=37;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.73634e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.1014G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=9/12,cDNA_position=1032,CDS_position=1014,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=338,Codons=ctG/ctA,MINIMISED=1,HGVSc=ENST00000258960.2:c.1014G>A
CDS|ENST00000258960	VCF	synonymous_variant	1054	1054	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-112;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06134e-06;Hom=0;AF_POPMAX=2.97885e-05;AN_POPMAX=33570;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41367e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.22222e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=90;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97885e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.1041A>G(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=9/12,cDNA_position=1059,CDS_position=1041,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=347,Codons=ccA/ccG,MINIMISED=1,HGVSc=ENST00000258960.2:c.1041A>G
CDS|ENST00000258960	VCF	synonymous_variant	1060	1060	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-82;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06124e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41334e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.27610e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000258960.2:c.1047G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=9/12,cDNA_position=1065,CDS_position=1047,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=349,Codons=gtG/gtA,MINIMISED=1,HGVSc=ENST00000258960.2:c.1047G>A
CDS|ENST00000258960	VCF	synonymous_variant	1075	1075	0.0	.	.	AC_Male=3;AF_NFE=8.95239e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|4|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94028e-59;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43661e-05;Hom=0;AF_POPMAX=1.48916e-04;AN_POPMAX=33576;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|1|2|0|1|1|0|0|0;AF_Male=2.22390e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=3.71530e-01;Hom_EAS=0;AC_AMR=5;AF_ASJ=0.00000e+00;DP_MEDIAN=67;AF_Female=2.69430e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.22228e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=1.48916e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.241e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.1062C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=9/12,ExAC_AMR_MAF=A:0,cDNA_position=1080,CDS_position=1062,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs751985902,VARIANT_CLASS=SNV,Protein_position=354,Codons=acC/acA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.1062C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	1078	1078	0.0	.	.	AC_Male=5;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|4|1|1|4|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-70;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.68519e-05;Hom=0;AF_POPMAX=4.16915e-04;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|1|1|2|1|1|3|1|1|1|0|0|0;AF_Male=3.70645e-05;AF_AFR=0.00000e+00;AC_raw=14;AB_MEDIAN=4.70918e-01;Hom_EAS=0;AC_AMR=14;AF_ASJ=0.00000e+00;DP_MEDIAN=59;AF_Female=8.08233e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=14;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.68477e-05;Hom_Female=0;AF_AMR=4.16915e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=R,HGVSp=ENST00000258960.2:c.1065G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=9/12,ExAC_AMR_MAF=A:0,cDNA_position=1083,CDS_position=1065,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs781580851,VARIANT_CLASS=SNV,Protein_position=355,Codons=agG/agA,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000258960.2:c.1065G>A,ExAC_Adj_MAF=A:0.0003456
CDS|ENST00000258960	VCF	synonymous_variant	1105	1105	0.0	.	.	AC_Male=6;AF_NFE=3.58057e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|3|3|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-65;AF_OTH=1.82415e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.46701e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|3|0|0|1|1|1|0|0|0|0|2|0|0;AF_Male=4.44774e-05;AF_AFR=0.00000e+00;AC_raw=11;AB_MEDIAN=3.98148e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=62;AF_Female=4.49035e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=6.49773e-05;AS_RF=9.34832e-01;Hom_AMR=0;AC_EAS=4;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=2;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:6.591e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:5.996e-05,AFR_MAF=T:0.0001211,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0002311,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.1092C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=9/12,ExAC_AMR_MAF=T:0,cDNA_position=1110,CDS_position=1092,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs769815313,VARIANT_CLASS=SNV,Protein_position=364,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:6.589e-05,HGVSc=ENST00000258960.2:c.1092C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1144	1144	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-36;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12466e-06;Hom=0;AF_POPMAX=6.49857e-05;AN_POPMAX=30776;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41554e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.53526e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=8.98376e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.49857e-05;AS_RF=9.31176e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.251e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.1131C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=9/12,ExAC_AMR_MAF=G:0,cDNA_position=1149,CDS_position=1131,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs749581366,VARIANT_CLASS=SNV,Protein_position=377,Codons=ccC/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.1131C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	1147	1147	0.0	.	.	AC_Male=2;AF_NFE=1.79112e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-80;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12460e-06;Hom=0;AF_POPMAX=1.79112e-05;AN_POPMAX=111662;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0;AF_Male=1.48304e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.07843e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08567e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=Q,HGVSp=ENST00000258960.2:c.1134G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=9/12,cDNA_position=1152,CDS_position=1134,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=378,Codons=caG/caA,MINIMISED=1,HGVSc=ENST00000258960.2:c.1134G>A
CDS|ENST00000258960	VCF	synonymous_variant	1159	1159	0.0	.	.	AC_Male=0;AF_NFE=8.96572e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-50;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06570e-06;Hom=0;AF_POPMAX=8.96572e-06;AN_POPMAX=111536;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.20690e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=8.99103e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19671e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=I,HGVSp=ENST00000258960.2:c.1146C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=9/12,cDNA_position=1164,CDS_position=1146,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=382,Codons=atC/atT,MINIMISED=1,HGVSc=ENST00000258960.2:c.1146C>T
CDS|ENST00000258960	VCF	synonymous_variant	1168	1168	0.0	.	.	AC_Male=4;AF_NFE=8.96861e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97631e-68;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62689e-05;Hom=0;AF_POPMAX=1.73933e-04;AN_POPMAX=17248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=2.96969e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.51825e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=87;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.37116e-01;Hom_AMR=0;AC_EAS=3;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.73933e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:1.664e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.507e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000258960.2:c.1155C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=9/12,ExAC_AMR_MAF=T:0,cDNA_position=1173,CDS_position=1155,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs768875089&COSM980093,VARIANT_CLASS=SNV,Protein_position=385,Codons=ttC/ttT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.1155C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1174	1174	0.0	.	.	AC_Male=1;AF_NFE=8.97811e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-131;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07047e-06;Hom=0;AF_POPMAX=8.97811e-06;AN_POPMAX=111382;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.42986e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.39326e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33934e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.345e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.51e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000258960.2:c.1161G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=9/12,ExAC_AMR_MAF=A:0,cDNA_position=1179,CDS_position=1161,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs774502405,VARIANT_CLASS=SNV,Protein_position=387,Codons=gtG/gtA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.1161G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	1186	1186	0.0	.	.	AC_Male=1;AF_NFE=2.71444e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|3|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-100;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.45570e-05;Hom=0;AF_POPMAX=5.80114e-05;AN_POPMAX=17238;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|1|0|0|0|0|0|1|0|0|1|0|0|0;AF_Male=7.47664e-06;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.79833e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=73;AF_Female=4.52161e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=3.27804e-05;AS_RF=9.44920e-01;Hom_AMR=0;AC_EAS=1;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80114e-05;AC_SAS=1;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43635e-05;Hom_Female=0;AF_AMR=2.99312e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.528e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0002,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.03e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000258960.2:c.1173C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1191,CDS_position=1173,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs369014766,VARIANT_CLASS=SNV,Protein_position=391,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000258960.2:c.1173C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1198	1198	0.0	.	.	AC_Male=3;AF_NFE=3.60529e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-44;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63157e-05;Hom=0;AF_POPMAX=3.60529e-05;AN_POPMAX=110948;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=2.23567e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.08621e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=59;AF_Female=9.01112e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05369e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.324e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.507e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.1185A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=G:0,cDNA_position=1203,CDS_position=1185,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs771817702,VARIANT_CLASS=SNV,Protein_position=395,Codons=acA/acG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.1185A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	1219	1219	0.0	.	.	AC_Male=4;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|1|0|4|2|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.58114e-48;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=4.48752e-05;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25698e-05;Hom=0;AF_POPMAX=2.28087e-04;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|1|1|0|0|0|0|0|1|1|0|0|0|0|0;AF_Male=2.97296e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.70158e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=52;AF_Female=3.60101e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=2.28087e-04;AS_RF=9.06358e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=7;POPMAX=SAS;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.476e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0001828,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.1206G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1224,CDS_position=1206,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746713731,VARIANT_CLASS=SNV,Protein_position=402,Codons=acG/acA,ExAC_AFR_MAF=A:2.471e-05,HGVSc=ENST00000258960.2:c.1206G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	1219	1219	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-28;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07123e-06;Hom=0;AF_POPMAX=3.25839e-05;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43240e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25839e-05;AS_RF=8.36271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.476e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0001828,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.1206G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1224,CDS_position=1206,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746713731,VARIANT_CLASS=SNV,Protein_position=402,Codons=acG/acT,ExAC_AFR_MAF=A:2.471e-05,HGVSc=ENST00000258960.2:c.1206G>T,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	1240	1240	0.0	.	.	AC_Male=1;AF_NFE=8.95528e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-103;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06147e-06;Hom=0;AF_POPMAX=8.95528e-06;AN_POPMAX=111666;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41411e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.13462e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=104;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.43219e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000258960.2:c.1227C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,cDNA_position=1245,CDS_position=1227,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=409,Codons=aaC/aaT,MINIMISED=1,HGVSc=ENST00000258960.2:c.1227C>T
CDS|ENST00000258960	VCF	synonymous_variant	1249	1249	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-269;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41048e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=229;AF_Female=8.98037e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.09084e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.1236C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1254,CDS_position=1236,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs759148893,VARIANT_CLASS=SNV,Protein_position=412,Codons=acC/acT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1236C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1261	1261	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-97;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=60;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.19242e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.1248C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,cDNA_position=1266,CDS_position=1248,SYMBOL=NMT1,Existing_variation=rs773592883,VARIANT_CLASS=SNV,Protein_position=416,Codons=ctC/ctT,MINIMISED=1,HGVSc=ENST00000258960.2:c.1248C>T
CDS|ENST00000258960	VCF	synonymous_variant	1282	1282	0.0	.	.	AC_Male=0;AF_NFE=8.95111e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-104;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12117e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.61430e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=185;AF_Female=1.79598e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.43594e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.236e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=Y,HGVSp=ENST00000258960.2:c.1269C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1287,CDS_position=1269,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764809965,VARIANT_CLASS=SNV,Protein_position=423,Codons=taC/taT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1269C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1285	1285	0.0	.	.	AC_Male=4;AF_NFE=9.84640e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|3|6|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-207;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=13;Hom_NFE=0;AF=5.27880e-05;Hom=0;AF_POPMAX=9.84640e-05;AN_POPMAX=111716;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;AF_Male=2.96498e-05;AF_AFR=0.00000e+00;AC_raw=13;AB_MEDIAN=4.68254e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=147;AF_Female=8.08190e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|13;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=NFE;AC_POPMAX=11;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.27872e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:5.765e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0002,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001049,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000258960.2:c.1272C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1290,CDS_position=1272,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs143838999,VARIANT_CLASS=SNV,Protein_position=424,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:5.765e-05,HGVSc=ENST00000258960.2:c.1272C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1321	1321	0.0	.	.	AC_Male=3;AF_NFE=2.68548e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-136;AF_OTH=3.64564e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03074e-05;Hom=0;AF_POPMAX=2.68548e-05;AN_POPMAX=111712;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|1;AF_Male=2.22397e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.47154e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=1.79659e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52266e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000258960.2:c.1308C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1326,CDS_position=1308,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766390878,VARIANT_CLASS=SNV,Protein_position=436,Codons=agC/agT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1308C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1324	1324	0.0	.	.	AC_Male=7;AF_NFE=2.68567e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|3|1|1|4|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-92;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=10;Hom_NFE=0;AF=4.06187e-05;Hom=0;AF_POPMAX=1.94919e-04;AN_POPMAX=30782;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|1|0|1|0|0|1|1|1;AF_Male=5.18988e-05;AF_AFR=6.53424e-05;AC_raw=11;AB_MEDIAN=4.30556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=100;AF_Female=2.69508e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|10;Hom_raw=0;AF_SAS=1.94919e-04;AS_RF=9.08157e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=6;POPMAX=SAS;AC_POPMAX=6;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.942e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:2.997e-05,AFR_MAF=T:0.0002422,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000258960.2:c.1311C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1329,CDS_position=1311,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754018187,VARIANT_CLASS=SNV,Protein_position=437,Codons=gaC/gaT,MINIMISED=1,ExAC_AFR_MAF=T:4.942e-05,HGVSc=ENST00000258960.2:c.1311C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1336	1336	0.0	.	.	AC_Male=4;AF_NFE=1.79067e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-126;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62555e-05;Hom=0;AF_POPMAX=1.15955e-04;AN_POPMAX=17248;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AF_Male=2.96665e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.64516e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=66;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41995e-01;Hom_AMR=0;AC_EAS=2;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.15955e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.1323C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,cDNA_position=1341,CDS_position=1323,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=441,Codons=ctC/ctT,MINIMISED=1,HGVSc=ENST00000258960.2:c.1323C>T
CDS|ENST00000258960	VCF	synonymous_variant	1339	1339	0.0	.	.	AC_Male=4;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|4|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-155;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25216e-05;Hom=0;AF_POPMAX=4.63822e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|1|0|0|0;AF_Male=2.96754e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.85450e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=3.59719e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36108e-01;Hom_AMR=0;AC_EAS=8;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=4.63822e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=8;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000258960.2:c.1326C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1344,CDS_position=1326,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778948819,VARIANT_CLASS=SNV,Protein_position=442,Codons=gcC/gcT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1326C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1375	1375	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98420e-125;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43637e-05;Hom=0;AF_POPMAX=1.78667e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3|1|1|0|1;AF_Male=2.22374e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.95800e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=2.69397e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43239e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=1.78667e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000258960.2:c.1362T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=C:0,cDNA_position=1380,CDS_position=1362,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs771722999,VARIANT_CLASS=SNV,Protein_position=454,Codons=gaT/gaC,MINIMISED=1,ExAC_AFR_MAF=C:1.647e-05,HGVSc=ENST00000258960.2:c.1362T>C,ExAC_Adj_MAF=C:0.0001729
CDS|ENST00000258960	VCF	synonymous_variant	1393	1393	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-79;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.23077e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=78;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.1380C>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=11/12,cDNA_position=1398,CDS_position=1380,SYMBOL=NMT1,Existing_variation=rs376284001,VARIANT_CLASS=SNV,Protein_position=460,Codons=acC/acA,MINIMISED=1,HGVSc=ENST00000258960.2:c.1380C>A
CDS|ENST00000258960	VCF	synonymous_variant	1396	1396	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-60;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12130e-06;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.41246e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.47362e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.50841e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,GMAF=T:0.0002,Amino_acids=F,HGVSp=ENST00000258960.2:c.1383C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=T:0,cDNA_position=1401,CDS_position=1383,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs556448466,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=461,AA_MAF=T:0.001,Codons=ttC/ttT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1383C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1399	1399	0.0	.	.	AC_Male=1;AF_NFE=1.79025e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-108;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12130e-06;Hom=0;AF_POPMAX=1.79025e-05;AN_POPMAX=111716;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.41246e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.68750e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=93;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.998e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.1386G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=A:0,cDNA_position=1404,CDS_position=1386,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs372878120,VARIANT_CLASS=SNV,Protein_position=462,Codons=ctG/ctA,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000258960.2:c.1386G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	synonymous_variant	1408	1408	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-134;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53424e-05;AC_raw=1;AB_MEDIAN=5.44304e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41092e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000258960.2:c.1395C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=G:9.61e-05,cDNA_position=1413,CDS_position=1395,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763355938,VARIANT_CLASS=SNV,Protein_position=465,Codons=ctC/ctG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.1395C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	synonymous_variant	1417	1417	0.0	.	.	AC_Male=3;AF_NFE=4.47555e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-85;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03034e-05;Hom=0;AF_POPMAX=4.47555e-05;AN_POPMAX=111718;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|1|1|1|0|0|1|0|0;AF_Male=2.22374e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.12195e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=66;AF_Female=1.79604e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20461e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000258960.2:c.1404C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=T,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=T:0,cDNA_position=1422,CDS_position=1404,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs369290804,VARIANT_CLASS=SNV,Protein_position=468,Codons=ggC/ggT,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000258960.2:c.1404C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1426	1426	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-125;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.21277e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08869e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=D,HGVSp=ENST00000258960.2:c.1413C>T(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/12,cDNA_position=1431,CDS_position=1413,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=471,Codons=gaC/gaT,MINIMISED=1,HGVSc=ENST00000258960.2:c.1413C>T
CDS|ENST00000258960	VCF	synonymous_variant	1453	1453	0.0	.	.	AC_Male=6;AF_NFE=1.79029e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|0|5|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-97;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=9;Hom_NFE=0;AF=3.65470e-05;Hom=0;AF_POPMAX=7.10804e-04;AN_POPMAX=9848;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|3|0|3|0|0|0|1;AF_Male=4.44754e-05;AF_AFR=0.00000e+00;AC_raw=9;AB_MEDIAN=5.10204e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=7.10804e-04;DP_MEDIAN=77;AF_Female=2.69416e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|9;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08147e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=7;AF_raw=3.65450e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=C:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:4.497e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000258960.2:c.1440T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,EA_MAF=C:0,Allele=C,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=C:0,cDNA_position=1458,CDS_position=1440,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs373214072,VARIANT_CLASS=SNV,Protein_position=480,Codons=aaT/aaC,MINIMISED=1,ExAC_AFR_MAF=C:2.471e-05,HGVSc=ENST00000258960.2:c.1440T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	synonymous_variant	1462	1462	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-54;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21834e-05;Hom=0;AF_POPMAX=9.74596e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=3.92157e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=51;AF_Female=2.69450e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=9.74596e-05;AS_RF=9.33552e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0001212,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=C,HGVSp=ENST00000258960.2:c.1449C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=T:0,cDNA_position=1467,CDS_position=1449,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs767877724,VARIANT_CLASS=SNV,Protein_position=483,Codons=tgC/tgT,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.1449C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	synonymous_variant	1465	1465	0.0	.	.	AC_Male=23;AF_NFE=9.84798e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|2|8|16|9|8|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-97;AF_OTH=3.64697e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=45;Hom_NFE=0;AF=1.82747e-04;Hom=0;AF_POPMAX=2.64013e-03;AN_POPMAX=9848;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|0|1|5|1|3|2|9|4|3|4|1|3|4;AF_Male=1.70497e-04;AF_AFR=0.00000e+00;AC_raw=45;AB_MEDIAN=4.87500e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=2.64013e-03;DP_MEDIAN=69;AF_Female=1.97589e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|45;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99273e-01;Hom_AMR=0;AC_EAS=0;AC_Female=22;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=26;AC_AFR=0;Hom_SAS=0;AC_ASJ=26;AF_raw=1.82725e-04;Hom_Female=0;AF_AMR=1.78667e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:0.0001401,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.000225,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000258960.2:c.1452C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=11/12,ExAC_AMR_MAF=T:0,cDNA_position=1470,CDS_position=1452,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs200139594&COSM3672473,VARIANT_CLASS=SNV,Protein_position=484,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:1.400e-04,HGVSc=ENST00000258960.2:c.1452C>T,ExAC_Adj_MAF=T:0.000173
CDS|ENST00000258960	VCF	synonymous_variant	1480	1480	0.0	.	.	AC_Male=1;AF_NFE=8.95608e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-115;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06220e-06;Hom=0;AF_POPMAX=8.95608e-06;AN_POPMAX=111656;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41455e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=90;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000258960.2:c.1467G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=11/12,cDNA_position=1485,CDS_position=1467,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=489,Codons=gaG/gaA,MINIMISED=1,HGVSc=ENST00000258960.2:c.1467G>A
CDS|ENST00000258960	VCF	synonymous_variant	1495	1495	0.0	.	.	AC_Male=6;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|3|0|1|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-82;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.85095e-05;Hom=0;AF_POPMAX=2.28624e-04;AN_POPMAX=30618;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|1|0|0|0|0|1|1|2|0|0;AF_Male=4.45778e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=9.01421e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=2.28624e-04;AS_RF=9.45417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=7;POPMAX=SAS;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84239e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=synonymous_variant,Amino_acids=V,HGVSp=ENST00000258960.2:c.1482G>A(p.%253D),STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=12/12,cDNA_position=1500,CDS_position=1482,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=494,Codons=gtG/gtA,MINIMISED=1,HGVSc=ENST00000258960.2:c.1482G>A
CDS|ENST00000258960	VCF	stop_gained	473	473	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=3.98107e-106;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=4.48511e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06412e-06;Hom=0;AF_POPMAX=4.48511e-05;AN_POPMAX=22296;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41983e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.88235e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=68;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.32793e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,LoF=HC,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,LoF_info=POSITION:0.308517773306506&ANN_ORF:521.9788&MAX_ORF:521.9788,Consequence=stop_gained,Amino_acids=Q/*,HGVSp=ENSP00000258960.2:p.Gln154Ter,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=HIGH,EXON=4/12,cDNA_position=478,CDS_position=460,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=154,Codons=Cag/Tag,MINIMISED=1,HGVSc=ENST00000258960.2:c.460C>T
CDS|ENST00000258960	VCF	stop_gained	1028	1028	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=5;AB_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.42754e-01;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=1.31183e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=0.00000e+00;GQ_HIST_ALT=1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.16590e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,LoF=HC,UNIPARC=UPI0000130275,PHENO=1,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,LoF_info=POSITION:0.68075117370892&ANN_ORF:626.8688&MAX_ORF:626.8688,Consequence=stop_gained,Amino_acids=R/*,HGVSp=ENSP00000258960.2:p.Arg339Ter,STRAND=1,CCDS=CCDS11494.1,SOMATIC=1,Allele=T,IMPACT=HIGH,EXON=9/12,cDNA_position=1033,CDS_position=1015,SYMBOL=NMT1,Existing_variation=COSM187889,VARIANT_CLASS=SNV,Protein_position=339,Codons=Cga/Tga,MINIMISED=1,HGVSc=ENST00000258960.2:c.1015C>T
CDS|ENST00000258960	ensembl_havana	CDS	14	144	0.0	+	0	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	145	253	0.0	+	1	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	254	398	0.0	+	0	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	399	517	0.0	+	2	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	518	609	0.0	+	0	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	610	726	0.0	+	1	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	727	897	0.0	+	1	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	898	1006	0.0	+	1	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	1007	1177	0.0	+	0	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	1178	1345	0.0	+	0	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	1346	1483	0.0	+	0	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	CDS	1484	1504	0.0	+	0	Parent=ENST00000258960;id=ENSP00000258960
CDS|ENST00000258960	ensembl_havana	exon	1	144	0.0	+	.	Parent=ENST00000258960;id=ENSE00001324312
CDS|ENST00000258960	ensembl_havana	exon	145	253	0.0	+	.	Parent=ENST00000258960;id=ENSE00003508836
CDS|ENST00000258960	ensembl_havana	exon	254	398	0.0	+	.	Parent=ENST00000258960;id=ENSE00003516529
CDS|ENST00000258960	ensembl_havana	exon	399	517	0.0	+	.	Parent=ENST00000258960;id=ENSE00003484461
CDS|ENST00000258960	ensembl_havana	exon	518	609	0.0	+	.	Parent=ENST00000258960;id=ENSE00003542284
CDS|ENST00000258960	ensembl_havana	exon	610	726	0.0	+	.	Parent=ENST00000258960;id=ENSE00003607442
CDS|ENST00000258960	ensembl_havana	exon	727	897	0.0	+	.	Parent=ENST00000258960;id=ENSE00003656469
CDS|ENST00000258960	ensembl_havana	exon	898	1006	0.0	+	.	Parent=ENST00000258960;id=ENSE00003849402
CDS|ENST00000258960	ensembl_havana	exon	1007	1177	0.0	+	.	Parent=ENST00000258960;id=ENSE00003849851
CDS|ENST00000258960	ensembl_havana	exon	1178	1345	0.0	+	.	Parent=ENST00000258960;id=ENSE00003846693
CDS|ENST00000258960	ensembl_havana	exon	1346	1483	0.0	+	.	Parent=ENST00000258960;id=ENSE00003844436
CDS|ENST00000258960	ensembl_havana	exon	1484	4881	0.0	+	.	Parent=ENST00000258960;id=ENSE00001110185
CDS|ENST00000258960	VCF	frameshift_variant	1419	1420	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.00000e-62;AF_OTH=0.00000e+00;alleles=TA%2CT;AF_FIN=4.48430e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=4.48430e-05;AN_POPMAX=22300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.62267e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,LoF=HC,UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,LoF_info=POSITION:0.943661971830986&ANN_ORF:396.74&MAX_ORF:396.74,Consequence=frameshift_variant,Amino_acids=I/X,HGVSp=ENSP00000258960.2:p.Ile469MetfsTer79,STRAND=1,CCDS=CCDS11494.1,Allele=-,IMPACT=HIGH,EXON=11/12,cDNA_position=1425,CDS_position=1407,SYMBOL=NMT1,VARIANT_CLASS=deletion,Protein_position=469,Codons=atA/at,MINIMISED=1,HGVSc=ENST00000258960.2:c.1407delA
CDS|ENST00000258960	VCF	missense_variant	18	18	0.0	.	.	AC_Male=0;AF_NFE=9.04748e-06;Hom_FIN=0;GQ_MEDIAN=20;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.90099e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.19363e-06;Hom=0;AF_POPMAX=3.00571e-05;AN_POPMAX=33270;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.81594e-05;GQ_HIST_ALT=0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.32038e-03;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=3.00571e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.651e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000258960.2:p.Ala2Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=23,CDS_position=5,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs771527303,VARIANT_CLASS=SNV,Protein_position=2,Codons=gCg/gTg,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000258960.2:c.5C>T,ExAC_Adj_MAF=T:8.965e-05
CDS|ENST00000258960	VCF	missense_variant	20	20	0.0	.	.	AC_Male=1;AF_NFE=9.02755e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-30;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.17307e-06;Hom=0;AF_POPMAX=6.58762e-05;AN_POPMAX=15180;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44923e-06;AF_AFR=6.58762e-05;AC_raw=2;AB_MEDIAN=4.35484e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=9.05272e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20566e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.622e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.564e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.823),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=D/H,HGVSp=ENSP00000258960.2:p.Asp3His,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=C:0,cDNA_position=25,CDS_position=7,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs772761859,VARIANT_CLASS=SNV,Protein_position=3,Codons=Gac/Cac,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000258960.2:c.7G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	23	23	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16887e-06;Hom=0;AF_POPMAX=6.51339e-05;AN_POPMAX=30706;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=1.80973e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.51339e-05;AS_RF=9.34226e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.069),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000258960.2:p.Glu4Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,cDNA_position=28,CDS_position=10,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=4,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000258960.2:c.10G>A
CDS|ENST00000258960	VCF	missense_variant	24	24	0.0	.	.	AC_Male=0;AF_NFE=9.01990e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08360e-06;Hom=0;AF_POPMAX=9.01990e-06;AN_POPMAX=110866;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=9.04732e-06;GQ_HIST_ALT=0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17447e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.595e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.559e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.066),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/G,HGVSp=ENSP00000258960.2:p.Glu4Gly,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=29,CDS_position=11,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs760309598,VARIANT_CLASS=SNV,Protein_position=4,Codons=gAg/gGg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.11A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	26	26	0.0	.	.	AC_Male=31;AF_NFE=9.01518e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|4|2|10|15|9|8|6|1|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.15479e-38;AF_OTH=3.66838e-04;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=56;Hom_NFE=0;AF=2.28573e-04;Hom=0;AF_POPMAX=3.07603e-03;AN_POPMAX=17230;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|3|15|10|7|8|3|3|1|4|1|1|0|0|0|0|0|0;AF_Male=2.30614e-04;AF_AFR=0.00000e+00;AC_raw=56;AB_MEDIAN=4.76557e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=2.26093e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|56;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.34281e-01;Hom_AMR=0;AC_EAS=53;AC_Female=25;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.07603e-03;AC_SAS=0;POPMAX=EAS;AC_POPMAX=53;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.27391e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.08),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:0.0002232,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,EAS_MAF=C:0,EUR_MAF=C:0.001,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0.002947,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=C:0.0002,Amino_acids=S/R,HGVSp=ENSP00000258960.2:p.Ser5Arg,STRAND=1,ExAC_SAS_MAF=C:0.001171,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=C:0,cDNA_position=31,CDS_position=13,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs564172691,SAS_MAF=C:0,VARIANT_CLASS=SNV,Protein_position=5,AA_MAF=C:0,Codons=Agt/Cgt,MINIMISED=1,ExAC_AFR_MAF=C:2.142e-04,HGVSc=ENST00000258960.2:c.13A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	27	27	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08090e-06;Hom=0;AF_POPMAX=3.25330e-05;AN_POPMAX=30738;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43760e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25330e-05;AS_RF=8.76833e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.39),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=S/N,HGVSp=ENSP00000258960.2:p.Ser5Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,cDNA_position=32,CDS_position=14,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=5,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000258960.2:c.14G>A
CDS|ENST00000258960	VCF	missense_variant	32	32	0.0	.	.	AC_Male=0;AF_NFE=9.01372e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-34;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08110e-06;Hom=0;AF_POPMAX=9.01372e-06;AN_POPMAX=110942;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.80000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.04454e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06165e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.623),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/P,HGVSp=ENSP00000258960.2:p.Thr7Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,cDNA_position=37,CDS_position=19,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=7,Codons=Aca/Cca,MINIMISED=1,HGVSc=ENST00000258960.2:c.19A>C
CDS|ENST00000258960	VCF	missense_variant	35	35	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52365e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.887),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000258960.2:p.Ala8Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,cDNA_position=40,CDS_position=22,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=Gca/Aca,HGVSc=ENST00000258960.2:c.22G>A
CDS|ENST00000258960	VCF	missense_variant	35	35	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-45;AF_OTH=1.83756e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08320e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.05108e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.37319e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.976),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/P,HGVSp=ENSP00000258960.2:p.Ala8Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,cDNA_position=40,CDS_position=22,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=Gca/Cca,HGVSc=ENST00000258960.2:c.22G>C
CDS|ENST00000258960	VCF	missense_variant	36	36	0.0	.	.	AC_Male=4;AF_NFE=9.02104e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-43;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63397e-05;Hom=0;AF_POPMAX=9.75864e-05;AN_POPMAX=30742;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=2.97699e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.70769e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=9.75864e-05;AS_RF=9.42769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.713e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.554e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.2),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000258960.2:p.Ala8Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=41,CDS_position=23,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764406772,VARIANT_CLASS=SNV,Protein_position=8,Codons=gCa/gTa,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.23C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	38	38	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-39;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08257e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=9.04846e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.15769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.28),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.556e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000258960.2:p.Val9Leu,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=C:0,cDNA_position=43,CDS_position=25,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs752105945,VARIANT_CLASS=SNV,Protein_position=9,Codons=Gtg/Ctg,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000258960.2:c.25G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	44	44	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.87339e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.63),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.554e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000258960.2:p.Pro11Ser,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=49,CDS_position=31,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=11,Codons=Ccg/Tcg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000258960.2:c.31C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	44	44	0.0	.	.	AC_Male=0;AF_NFE=9.02006e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38634e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08397e-06;Hom=0;AF_POPMAX=9.02006e-06;AN_POPMAX=110864;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.70833e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=18;AF_Female=9.05403e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.26525e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.49),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.554e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.007),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/T,HGVSp=ENSP00000258960.2:p.Pro11Thr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=49,CDS_position=31,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=11,Codons=Ccg/Acg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000258960.2:c.31C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	45	45	0.0	.	.	AC_Male=2;AF_NFE=9.01664e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-48;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16573e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48792e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63469e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.40560e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.3),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.552e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000258960.2:p.Pro11Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=50,CDS_position=32,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs750513385,VARIANT_CLASS=SNV,Protein_position=11,Codons=cCg/cTg,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.32C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	48	48	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=62;AB_HIST_ALT=0|0|2|0|0|2|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25280e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22474e-05;Hom=0;AF_POPMAX=6.50703e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|1|0|2|0|1|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44025e-06;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=1.80920e-05;GQ_HIST_ALT=1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.50703e-05;AS_RF=1.16160e-02;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=2.98401e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000258960.2:p.Pro12Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=53,CDS_position=35,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=12,Codons=cCg/cTg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.35C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	48	48	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=58;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.80083e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08247e-06;Hom=0;AF_POPMAX=3.25351e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.95563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=9.04601e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25351e-05;AS_RF=1.45870e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.3),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.093),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/Q,HGVSp=ENSP00000258960.2:p.Pro12Gln,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=53,CDS_position=35,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=12,Codons=cCg/cAg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.35C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	50	50	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-63;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08007e-06;Hom=0;AF_POPMAX=5.80181e-05;AN_POPMAX=17236;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60976e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96821e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.09),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.053),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/P,HGVSp=ENSP00000258960.2:p.Ala13Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,cDNA_position=55,CDS_position=37,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=13,Codons=Gca/Cca,MINIMISED=1,HGVSc=ENST00000258960.2:c.37G>C
CDS|ENST00000258960	VCF	missense_variant	53	53	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97164e-32;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15627e-06;Hom=0;AF_POPMAX=1.16063e-04;AN_POPMAX=17232;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.57018e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80682e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52227e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.16063e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.49),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.534e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.035),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001174,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000258960.2:p.Pro14Ser,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=58,CDS_position=40,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754859910,VARIANT_CLASS=SNV,Protein_position=14,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000258960.2:c.40C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	54	54	0.0	.	.	AC_Male=1;AF_NFE=2.69964e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.37387e-64;AF_OTH=1.83217e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63090e-05;Hom=0;AF_POPMAX=2.69964e-05;AN_POPMAX=111126;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.03446e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=2.70929e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36654e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.33),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000258960.2:p.Pro14Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=1/12,cDNA_position=59,CDS_position=41,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=14,Codons=cCt/cTt,MINIMISED=1,HGVSc=ENST00000258960.2:c.41C>T
CDS|ENST00000258960	VCF	missense_variant	57	57	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-53;AF_OTH=1.83083e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22264e-05;Hom=0;AF_POPMAX=6.58068e-05;AN_POPMAX=15196;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43262e-06;AF_AFR=6.58068e-05;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=1.80460e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35197e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.705e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0.0014,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=T:0.0002,Amino_acids=P/L,HGVSp=ENSP00000258960.2:p.Pro15Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=T:0.0001013,cDNA_position=62,CDS_position=44,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs202061902,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=15,AA_MAF=T:0,Codons=cCg/cTg,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.44C>T,ExAC_Adj_MAF=T:8.969e-05
CDS|ENST00000258960	VCF	missense_variant	60	60	0.0	.	.	AC_Male=1;AF_NFE=8.98893e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-25;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07236e-06;Hom=0;AF_POPMAX=8.98893e-06;AN_POPMAX=111248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42765e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.62500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.15),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.703e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.089e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/R,HGVSp=ENSP00000258960.2:p.Leu16Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=65,CDS_position=47,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772038652,VARIANT_CLASS=SNV,Protein_position=16,Codons=cTg/cGg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.47T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	69	69	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-33;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14120e-06;Hom=0;AF_POPMAX=5.96019e-05;AN_POPMAX=33556;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42589e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.78231e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=5.96019e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.94),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000258960.2:p.Met19Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,cDNA_position=74,CDS_position=56,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=19,Codons=aTg/aGg,HGVSc=ENST00000258960.2:c.56T>G
CDS|ENST00000258960	VCF	missense_variant	69	69	0.0	.	.	AC_Male=0;AF_NFE=8.98650e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-65;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07060e-06;Hom=0;AF_POPMAX=8.98650e-06;AN_POPMAX=111278;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43341e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.17),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.01),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/T,HGVSp=ENSP00000258960.2:p.Met19Thr,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,cDNA_position=74,CDS_position=56,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=19,Codons=aTg/aCg,HGVSc=ENST00000258960.2:c.56T>C
CDS|ENST00000258960	VCF	missense_variant	72	72	0.0	.	.	AC_Male=7;AF_NFE=9.88373e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|3|1|3|3|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-45;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.47784e-05;Hom=0;AF_POPMAX=9.88373e-05;AN_POPMAX=111294;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|4|0|1|0|2|0|1|0|1|0|0|0|0;AF_Male=5.19889e-05;AF_AFR=0.00000e+00;AC_raw=11;AB_MEDIAN=4.18860e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.60328e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=11;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.14),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:7.653e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0.0001388,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.012),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000258960.2:p.Met20Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=77,CDS_position=59,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772952636,VARIANT_CLASS=SNV,Protein_position=20,Codons=aTg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:7.413e-05,HGVSc=ENST00000258960.2:c.59T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	83	83	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=52;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.20127e-01;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07090e-06;Hom=0;AF_POPMAX=2.98098e-05;AN_POPMAX=33546;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.16667e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.00836e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.23972e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=2.98098e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.52e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.07),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/R,HGVSp=ENSP00000258960.2:p.Gly24Arg,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=88,CDS_position=70,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746539074,VARIANT_CLASS=SNV,Protein_position=24,Codons=Ggg/Agg,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000258960.2:c.70G>A,ExAC_Adj_MAF=A:9.027e-05
CDS|ENST00000258960	VCF	missense_variant	84	84	0.0	.	.	AC_Male=1;AF_NFE=8.98182e-06;Hom_FIN=0;GQ_MEDIAN=54;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.54545e-02;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98182e-06;AN_POPMAX=111336;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42688e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.26923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.37827e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.47),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/A,HGVSp=ENSP00000258960.2:p.Gly24Ala,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,cDNA_position=89,CDS_position=71,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=24,Codons=gGg/gCg,MINIMISED=1,HGVSc=ENST00000258960.2:c.71G>C
CDS|ENST00000258960	VCF	missense_variant	89	89	0.0	.	.	AC_Male=0;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.53267e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07070e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.38095e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.00722e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.31156e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.529e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.546e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000258960.2:p.Gly26Ser,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=94,CDS_position=76,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs770300796,VARIANT_CLASS=SNV,Protein_position=26,Codons=Ggc/Agc,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000258960.2:c.76G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	94	94	0.0	.	.	AC_Male=1;AF_NFE=8.98101e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98101e-06;AN_POPMAX=111346;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42721e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.37664e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.73),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.539e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.547e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.493),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=H/Q,HGVSp=ENSP00000258960.2:p.His27Gln,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=99,CDS_position=81,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs776300314,VARIANT_CLASS=SNV,Protein_position=27,Codons=caT/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.81T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	96	96	0.0	.	.	AC_Male=0;AF_NFE=8.98505e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.31688e-02;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07130e-06;Hom=0;AF_POPMAX=8.98505e-06;AN_POPMAX=111296;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.51984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.00690e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.21757e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,PHENO=1,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/V,HGVSp=ENSP00000258960.2:p.Glu28Val,STRAND=1,CCDS=CCDS11494.1,SOMATIC=1,Allele=T,IMPACT=MODERATE,EXON=1/12,cDNA_position=101,CDS_position=83,SYMBOL=NMT1,Existing_variation=COSM1128678,VARIANT_CLASS=SNV,Protein_position=28,Codons=gAg/gTg,MINIMISED=1,HGVSc=ENST00000258960.2:c.83A>T
CDS|ENST00000258960	VCF	missense_variant	100	100	0.0	.	.	AC_Male=0;AF_NFE=8.98957e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-73;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07286e-06;Hom=0;AF_POPMAX=8.98957e-06;AN_POPMAX=111240;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.37037e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=9.01128e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05502e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.13),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.571e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.553e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.397),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=H/Q,HGVSp=ENSP00000258960.2:p.His29Gln,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=105,CDS_position=87,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759161485,VARIANT_CLASS=SNV,Protein_position=29,Codons=caC/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.87C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	102	102	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-32;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07425e-06;Hom=0;AF_POPMAX=5.80518e-05;AN_POPMAX=17226;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43362e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.34667e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80518e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.588e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.781),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001181,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=C/Y,HGVSp=ENSP00000258960.2:p.Cys30Tyr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=107,CDS_position=89,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764495116,VARIANT_CLASS=SNV,Protein_position=30,Codons=tGc/tAc,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000258960.2:c.89G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	104	104	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-26;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22221e-05;Hom=0;AF_POPMAX=8.96111e-05;AN_POPMAX=33478;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43329e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.21053e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.80297e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.53191e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=8.96111e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.55),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.721e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.248),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=S/G,HGVSp=ENSP00000258960.2:p.Ser31Gly,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=109,CDS_position=91,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774684452,VARIANT_CLASS=SNV,Protein_position=31,Codons=Agc/Ggc,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.91A>G,ExAC_Adj_MAF=G:0.0001836
CDS|ENST00000258960	VCF	missense_variant	133	133	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-29;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=3.26861e-05;AN_POPMAX=30594;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.47005e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.26861e-05;AS_RF=8.82577e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.21),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.018e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=S/R,HGVSp=ENSP00000258960.2:p.Ser40Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=138,CDS_position=120,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=40,Codons=agC/agG,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.120C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	135	135	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92478e-20;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09799e-06;Hom=0;AF_POPMAX=5.83158e-05;AN_POPMAX=17148;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.91667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07293e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.95804e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.83158e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.058e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.293),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.0001227,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=Y/C,HGVSp=ENSP00000258960.2:p.Tyr41Cys,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=140,CDS_position=122,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756247053,VARIANT_CLASS=SNV,Protein_position=41,Codons=tAc/tGc,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.122A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	138	138	0.0	.	.	AC_Male=1;AF_NFE=9.07738e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-55;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.11265e-06;Hom=0;AF_POPMAX=9.07738e-06;AN_POPMAX=110164;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49805e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.29412e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.17479e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06068e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.93),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000258960.2:p.Asn42Ser,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=1/12,cDNA_position=143,CDS_position=125,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=42,Codons=aAc/aGc,MINIMISED=1,HGVSc=ENST00000258960.2:c.125A>G
CDS|ENST00000258960	VCF	missense_variant	141	141	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=7;AB_HIST_ALT=0|0|2|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.66338e-01;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=4.53227e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12712e-06;Hom=0;AF_POPMAX=4.53227e-05;AN_POPMAX=22064;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.52298e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.73728e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21819e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.125),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/P,HGVSp=ENSP00000258960.2:p.Arg43Pro,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=1/12,cDNA_position=146,CDS_position=128,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=43,Codons=cGg/cCg,MINIMISED=1,HGVSc=ENST00000258960.2:c.128G>C
CDS|ENST00000258960	VCF	missense_variant	149	149	0.0	.	.	AC_Male=1;AF_NFE=9.20793e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-78;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13846e-06;Hom=0;AF_POPMAX=9.20793e-06;AN_POPMAX=108602;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.53477e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=50;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.26429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09934e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.76),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.304e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.508e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.037),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000258960.2:p.Leu46Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=G:0,cDNA_position=154,CDS_position=136,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs758247752,VARIANT_CLASS=SNV,Protein_position=46,Codons=Ttg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.136T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	150	150	0.0	.	.	AC_Male=1;AF_NFE=9.20082e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-91;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13363e-06;Hom=0;AF_POPMAX=9.20082e-06;AN_POPMAX=108686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.52627e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.83900e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.05),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.624),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/W,HGVSp=ENSP00000258960.2:p.Leu46Trp,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/12,cDNA_position=155,CDS_position=137,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=46,Codons=tTg/tGg,MINIMISED=1,HGVSc=ENST00000258960.2:c.137T>G
CDS|ENST00000258960	VCF	missense_variant	153	153	0.0	.	.	AC_Male=1;AF_NFE=9.18628e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-41;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12361e-06;Hom=0;AF_POPMAX=9.18628e-06;AN_POPMAX=108858;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.50875e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.88840e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09927e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.073),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=S/N,HGVSp=ENSP00000258960.2:p.Ser47Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/12,cDNA_position=158,CDS_position=140,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=47,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000258960.2:c.140G>A
CDS|ENST00000258960	VCF	missense_variant	155	155	0.0	.	.	AC_Male=0;AF_NFE=9.18577e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-80;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12368e-06;Hom=0;AF_POPMAX=9.18577e-06;AN_POPMAX=108864;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=9.14645e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40367e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.2),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000258960.2:p.Pro48Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/12,cDNA_position=160,CDS_position=142,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=48,Codons=Cca/Gca,MINIMISED=1,HGVSc=ENST00000258960.2:c.142C>G
CDS|ENST00000258960	VCF	missense_variant	161	161	0.0	.	.	AC_Male=6;AF_NFE=4.58573e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|3|2|4|8|1|1|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-54;AF_OTH=1.83352e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=21;Hom_NFE=0;AF=8.63501e-05;Hom=0;AF_POPMAX=9.81804e-04;AN_POPMAX=15278;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|2|5|2|2|2|0|3|0|0|1|0|1|0|0|1;AF_Male=4.49384e-05;AF_AFR=9.81804e-04;AC_raw=21;AB_MEDIAN=5.21739e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=1.36761e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|21;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=15;AC_AFR=15;Hom_SAS=0;AC_ASJ=0;AF_raw=8.60860e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.71),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.336e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=G:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.034e-05,AFR_MAF=G:0,SWISSPROT=P30419,EAS_MAF=G:0,EUR_MAF=G:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=G:0.0002,Amino_acids=N/D,HGVSp=ENSP00000258960.2:p.Asn50Asp,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,EA_MAF=G:0.0011,Allele=G,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=G:0.000789,cDNA_position=166,CDS_position=148,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs140455291,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=50,AA_MAF=G:0,Codons=Aat/Gat,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-05,HGVSc=ENST00000258960.2:c.148A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	162	162	0.0	.	.	AC_Male=2;AF_NFE=5.50327e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.29463e-76;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.46765e-05;Hom=0;AF_POPMAX=5.50327e-05;AN_POPMAX=109026;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AF_Male=1.49817e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.64551e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=3.64797e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53507e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.45964e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.45),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:2.508e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:4.569e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.017),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000258960.2:p.Asn50Ser,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=G:0,cDNA_position=167,CDS_position=149,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs757177482,VARIANT_CLASS=SNV,Protein_position=50,Codons=aAt/aGt,MINIMISED=1,ExAC_AFR_MAF=G:2.471e-05,HGVSc=ENST00000258960.2:c.149A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	174	174	0.0	.	.	AC_Male=3;AF_NFE=4.59441e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|2|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-54;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.05744e-05;Hom=0;AF_POPMAX=4.59441e-05;AN_POPMAX=108828;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|2|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24908e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.80645e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.82428e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99531e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.04965e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.11),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:4.372e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.027e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000258960.2:p.Ala54Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=T:0,cDNA_position=179,CDS_position=161,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs780748535,VARIANT_CLASS=SNV,Protein_position=54,Codons=gCc/gTc,MINIMISED=1,ExAC_AFR_MAF=T:4.118e-05,HGVSc=ENST00000258960.2:c.161C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	177	177	0.0	.	.	AC_Male=6;AF_NFE=6.46365e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|1|0|3|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-50;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.88843e-05;Hom=0;AF_POPMAX=6.46365e-05;AN_POPMAX=108298;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|2|1|1|0|0|0|0|0|1|0|0|0|0;AF_Male=4.50857e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.32432e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=9.15198e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.86984e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=possibly_damaging(0.72),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=K/R,HGVSp=ENSP00000258960.2:p.Lys55Arg,STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=T:0&G:0,cDNA_position=182,CDS_position=164,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=55,Codons=aAa/aGa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000258960.2:c.164A>G,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000258960	VCF	missense_variant	177	177	0.0	.	.	AC_Male=1;AF_NFE=9.23378e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-64;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12633e-06;Hom=0;AF_POPMAX=9.23378e-06;AN_POPMAX=108298;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.51428e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.22727e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09977e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.033),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=K/I,HGVSp=ENSP00000258960.2:p.Lys55Ile,STRAND=1,ExAC_SAS_MAF=T:0&G:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=T:0&G:0,cDNA_position=182,CDS_position=164,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=55,Codons=aAa/aTa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000258960.2:c.164A>T,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000258960	VCF	missense_variant	189	189	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-24;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15155e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.12500e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=9.21302e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=2.89217e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10004e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.08),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=K/R,HGVSp=ENSP00000258960.2:p.Lys59Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/12,cDNA_position=194,CDS_position=176,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=59,Codons=aAg/aGg,MINIMISED=1,HGVSc=ENST00000258960.2:c.176A>G
CDS|ENST00000258960	VCF	missense_variant	206	206	0.0	.	.	AC_Male=0;AF_NFE=9.88807e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-130;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.33099e-06;Hom=0;AF_POPMAX=9.88807e-06;AN_POPMAX=101132;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.14563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=9.61908e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33183e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10129e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.38),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.315e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.529e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.013),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=K/E,HGVSp=ENSP00000258960.2:p.Lys65Glu,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=G:0,cDNA_position=211,CDS_position=193,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779784731,VARIANT_CLASS=SNV,Protein_position=65,Codons=Aaa/Gaa,MINIMISED=1,ExAC_AFR_MAF=G:8.261e-06,HGVSc=ENST00000258960.2:c.193A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	216	216	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30719e-25;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.87099e-05;Hom=0;AF_POPMAX=1.31596e-04;AN_POPMAX=30396;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.55437e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.49730e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.03795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66438e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64119e-05;Hom_Female=0;AF_AMR=1.31596e-04;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.043),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/V,HGVSp=ENSP00000258960.2:p.Gly68Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/12,cDNA_position=221,CDS_position=203,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=68,Codons=gGc/gTc,MINIMISED=1,HGVSc=ENST00000258960.2:c.203G>T
CDS|ENST00000258960	VCF	missense_variant	233	233	0.0	.	.	AC_Male=1;AF_NFE=2.58685e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-31;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.06140e-05;Hom=0;AF_POPMAX=2.58685e-05;AN_POPMAX=77314;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=9.69330e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.87363e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.17280e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.91480e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.21760e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.19),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.017),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/S,HGVSp=ENSP00000258960.2:p.Ala74Ser,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/12,cDNA_position=238,CDS_position=220,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=74,Codons=Gcc/Tcc,MINIMISED=1,HGVSc=ENST00000258960.2:c.220G>T
CDS|ENST00000258960	VCF	missense_variant	234	234	0.0	.	.	AC_Male=0;AF_NFE=1.30774e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.34920e-06;Hom=0;AF_POPMAX=1.30774e-05;AN_POPMAX=76468;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.84615e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=65;AF_Female=1.18189e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.26907e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10985e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.15),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000258960.2:p.Ala74Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=2/12,cDNA_position=239,CDS_position=221,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=74,Codons=gCc/gTc,MINIMISED=1,HGVSc=ENST00000258960.2:c.221C>T
CDS|ENST00000258960	VCF	missense_variant	238	238	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-72;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.55759e-06;Hom=0;AF_POPMAX=3.91972e-05;AN_POPMAX=25512;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.22730e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.91972e-05;AS_RF=8.51470e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11306e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.12),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.163),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=Q/H,HGVSp=ENSP00000258960.2:p.Gln75His,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=2/12,cDNA_position=243,CDS_position=225,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=75,Codons=caG/caC,MINIMISED=1,HGVSc=ENST00000258960.2:c.225G>C
CDS|ENST00000258960	VCF	missense_variant	242	242	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=70;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97133e-05;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.12740e-05;Hom=0;AF_POPMAX=8.46453e-05;AN_POPMAX=11814;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.03086e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.94118e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=1.24387e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.04301e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=8.46453e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.23113e-06;Hom_Female=0;AF_AMR=3.93236e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.43),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.006),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=Q/K,HGVSp=ENSP00000258960.2:p.Gln77Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/12,cDNA_position=247,CDS_position=229,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=77,Codons=Cag/Aag,MINIMISED=1,HGVSc=ENST00000258960.2:c.229C>A
CDS|ENST00000258960	VCF	missense_variant	248	248	0.0	.	.	AC_Male=1;AF_NFE=2.98686e-05;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|2|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.19832e-05;Hom=0;AF_POPMAX=2.98686e-05;AN_POPMAX=66960;AC_NFE=2;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.09965e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.15047e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.31645e-05;GQ_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.22455e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64978e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.11),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.776e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:5.974e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.007),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/M,HGVSp=ENSP00000258960.2:p.Val79Met,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=2/12,ExAC_AMR_MAF=A:0,cDNA_position=253,CDS_position=235,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761306458,VARIANT_CLASS=SNV,Protein_position=79,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.569e-06,HGVSc=ENST00000258960.2:c.235G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	254	254	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-33;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.41163e-06;Hom=0;AF_POPMAX=6.76636e-05;AN_POPMAX=29558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.53130e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.32389e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.76636e-05;AS_RF=8.96351e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12123e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.81),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.681e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.000128,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=M/V,HGVSp=ENSP00000258960.2:p.Met81Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=G:0,cDNA_position=259,CDS_position=241,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767459577,VARIANT_CLASS=SNV,Protein_position=81,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.241A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	258	258	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51591e-22;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.09459e-05;AN_POPMAX=16408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.23913e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20091e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.09459e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.48),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.391e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=N/T,HGVSp=ENSP00000258960.2:p.Asn82Thr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=C,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=263,CDS_position=245,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=82,Codons=aAc/aCc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.245A>C,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	258	258	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-62;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.67646e-05;AN_POPMAX=14978;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.67646e-05;AC_raw=1;AB_MEDIAN=3.09859e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.02337e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.18),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.391e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=N/I,HGVSp=ENSP00000258960.2:p.Asn82Ile,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=263,CDS_position=245,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=82,Codons=aAc/aTc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.245A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	280	280	0.0	.	.	AC_Male=1;AF_NFE=9.04977e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-52;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10988e-06;Hom=0;AF_POPMAX=9.04977e-06;AN_POPMAX=110500;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49524e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.10256e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.90362e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.13),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.312e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.51e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=I/M,HGVSp=ENSP00000258960.2:p.Ile89Met,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=G:0,cDNA_position=285,CDS_position=267,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779405921,VARIANT_CLASS=SNV,Protein_position=89,Codons=atC/atG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.267C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	299	299	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-21;AF_OTH=1.83554e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08013e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.70588e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=9.03130e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.67445e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.29),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000258960.2:p.Ile96Val,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/12,cDNA_position=304,CDS_position=286,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=96,Codons=Att/Gtt,MINIMISED=1,HGVSc=ENST00000258960.2:c.286A>G
CDS|ENST00000258960	VCF	missense_variant	315	315	0.0	.	.	AC_Male=0;AF_NFE=8.97263e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-62;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07163e-06;Hom=0;AF_POPMAX=8.97263e-06;AN_POPMAX=111450;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=48;AF_Female=9.00739e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.18),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.258e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.129),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/E,HGVSp=ENSP00000258960.2:p.Val101Glu,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=A:0,cDNA_position=320,CDS_position=302,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs778561485,VARIANT_CLASS=SNV,Protein_position=101,Codons=gTg/gAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.302T>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	317	317	0.0	.	.	AC_Male=0;AF_NFE=8.97167e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-66;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07073e-06;Hom=0;AF_POPMAX=8.97167e-06;AN_POPMAX=111462;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.45455e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00414e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97942e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.41),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.258e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/C,HGVSp=ENSP00000258960.2:p.Gly102Cys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=T:0,cDNA_position=322,CDS_position=304,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs747390700,VARIANT_CLASS=SNV,Protein_position=102,Codons=Ggt/Tgt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.304G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	322	322	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-48;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07186e-06;Hom=0;AF_POPMAX=3.25563e-05;AN_POPMAX=30716;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43097e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25563e-05;AS_RF=9.07079e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.256e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.015),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=Q/H,HGVSp=ENSP00000258960.2:p.Gln103His,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=C:0,cDNA_position=327,CDS_position=309,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs771371139,VARIANT_CLASS=SNV,Protein_position=103,Codons=caG/caC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.309G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	323	323	0.0	.	.	AC_Male=1;AF_NFE=8.97392e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07279e-06;Hom=0;AF_POPMAX=8.97392e-06;AN_POPMAX=111434;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43152e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.97872e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.42544e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:8.254e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.067),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=A:0.0002,Amino_acids=G/R,HGVSp=ENSP00000258960.2:p.Gly104Arg,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=A:0,cDNA_position=328,CDS_position=310,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs563736659&COSM1493963,SAS_MAF=A:0.001,VARIANT_CLASS=SNV,Protein_position=104,AA_MAF=A:0,Codons=Gga/Aga,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.310G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	339	339	0.0	.	.	AC_Male=1;AF_NFE=8.98053e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-63;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07515e-06;Hom=0;AF_POPMAX=8.98053e-06;AN_POPMAX=111352;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43528e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.03846e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=52;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18859e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.35),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.249e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.501e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/T,HGVSp=ENSP00000258960.2:p.Met109Thr,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=C:0,cDNA_position=344,CDS_position=326,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs770043528,VARIANT_CLASS=SNV,Protein_position=109,Codons=aTg/aCg,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.326T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	350	350	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=7.94328e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=4.48632e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07581e-06;Hom=0;AF_POPMAX=4.48632e-05;AN_POPMAX=22290;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43572e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.25000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.10681e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.31),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=S/G,HGVSp=ENSP00000258960.2:p.Ser113Gly,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=3/12,cDNA_position=355,CDS_position=337,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=113,Codons=Agc/Ggc,MINIMISED=1,HGVSc=ENST00000258960.2:c.337A>G
CDS|ENST00000258960	VCF	missense_variant	357	357	0.0	.	.	AC_Male=1;AF_NFE=1.79727e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-36;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15328e-06;Hom=0;AF_POPMAX=1.79727e-05;AN_POPMAX=111280;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=9.02120e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.61453e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.259e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.155),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/L,HGVSp=ENSP00000258960.2:p.Arg115Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=T:0,cDNA_position=362,CDS_position=344,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs377156745&COSM436718,VARIANT_CLASS=SNV,Protein_position=115,Codons=cGa/cTa,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.344G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	359	359	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07525e-06;Hom=0;AF_POPMAX=3.25839e-05;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43550e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25839e-05;AS_RF=7.10677e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.66),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=S/R,HGVSp=ENSP00000258960.2:p.Ser116Arg,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=3/12,cDNA_position=364,CDS_position=346,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=116,Codons=Agc/Cgc,MINIMISED=1,HGVSc=ENST00000258960.2:c.346A>C
CDS|ENST00000258960	VCF	missense_variant	378	378	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.91433e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.37719e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.02383e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.859),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/M,HGVSp=ENSP00000258960.2:p.Thr122Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=T:0,cDNA_position=383,CDS_position=365,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=122,Codons=aCg/aTg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.365C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	378	378	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-14;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.51858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.945),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/R,HGVSp=ENSP00000258960.2:p.Thr122Arg,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=G,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=T:0,cDNA_position=383,CDS_position=365,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=122,Codons=aCg/aGg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.365C>G,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	386	386	0.0	.	.	AC_Male=0;AF_NFE=9.10167e-06;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|2|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13213e-06;Hom=0;AF_POPMAX=9.10167e-06;AN_POPMAX=109870;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=9.15131e-06;GQ_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.57813e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.387e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.253),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/I,HGVSp=ENSP00000258960.2:p.Val125Ile,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=A:0,cDNA_position=391,CDS_position=373,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761622308,VARIANT_CLASS=SNV,Protein_position=125,Codons=Gtc/Atc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.373G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	393	393	0.0	.	.	AC_Male=5;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|5|2|2|3|0|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-65;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.79897e-05;Hom=0;AF_POPMAX=9.23483e-04;AN_POPMAX=15160;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|3|1|1|1|0|0|0|0|1|1|1|2|0|1|0|1|1|1;AF_Male=3.77729e-05;AF_AFR=9.23483e-04;AC_raw=15;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=8.25294e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36291e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=14;AC_AFR=14;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:0.0001096,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=K/R,HGVSp=ENSP00000258960.2:p.Lys127Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,EA_MAF=G:0.0014,Allele=G,IMPACT=MODERATE,EXON=3/12,ExAC_AMR_MAF=G:0.001254,cDNA_position=398,CDS_position=380,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs144433221,VARIANT_CLASS=SNV,Protein_position=127,Codons=aAg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:1.071e-04,HGVSc=ENST00000258960.2:c.380A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	405	405	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-43;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06782e-06;Hom=0;AF_POPMAX=3.24950e-05;AN_POPMAX=30774;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42677e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.40426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24950e-05;AS_RF=7.83979e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/E,HGVSp=ENSP00000258960.2:p.Val131Glu,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=4/12,cDNA_position=410,CDS_position=392,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=131,Codons=gTg/gAg,MINIMISED=1,HGVSc=ENST00000258960.2:c.392T>A
CDS|ENST00000258960	VCF	missense_variant	416	416	0.0	.	.	AC_Male=1;AF_NFE=1.79398e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-64;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13028e-06;Hom=0;AF_POPMAX=1.79398e-05;AN_POPMAX=111484;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0;AF_Male=7.42148e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.25373e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=67;AF_Female=8.98876e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13408e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.657e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.015e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.011),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=H/Y,HGVSp=ENSP00000258960.2:p.His135Tyr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=T:0,cDNA_position=421,CDS_position=403,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs753759265,VARIANT_CLASS=SNV,Protein_position=135,Codons=Cat/Tat,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.403C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	425	425	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-36;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21939e-05;Hom=0;AF_POPMAX=1.15969e-04;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AF_Male=7.42027e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.77324e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=1.79762e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=3.24907e-05;AS_RF=8.84156e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.15969e-04;AC_SAS=1;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.272e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.111),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/M,HGVSp=ENSP00000258960.2:p.Val138Met,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=A:0,cDNA_position=430,CDS_position=412,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs752448187,VARIANT_CLASS=SNV,Protein_position=138,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000258960.2:c.412G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	431	431	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-75;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06372e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.15584e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=8.98521e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.41661e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.265e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.025),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000258960.2:p.Pro140Ser,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=T:0,cDNA_position=436,CDS_position=418,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs758111913,VARIANT_CLASS=SNV,Protein_position=140,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.418C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	432	432	0.0	.	.	AC_Male=0;AF_NFE=8.96363e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-36;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06355e-06;Hom=0;AF_POPMAX=8.96363e-06;AN_POPMAX=111562;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41176e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00024e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.032),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000258960.2:p.Pro140Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=4/12,cDNA_position=437,CDS_position=419,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=140,Codons=cCt/cTt,MINIMISED=1,HGVSc=ENST00000258960.2:c.419C>T
CDS|ENST00000258960	VCF	missense_variant	434	434	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-72;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21915e-05;Hom=0;AF_POPMAX=1.73933e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|1|0|0|0|1|0|0|0|0|0|0;AF_Male=1.48381e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.76190e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98586e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=3;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.73933e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.29),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:1.653e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0.001,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.015),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0002313,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=A:0.0002,Amino_acids=D/N,HGVSp=ENSP00000258960.2:p.Asp141Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=A:0,cDNA_position=439,CDS_position=421,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs201386803&COSM349346,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=141,AA_MAF=A:0,Codons=Gac/Aac,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000258960.2:c.421G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	455	455	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-54;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62509e-05;Hom=0;AF_POPMAX=1.19119e-04;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|2|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41697e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.40000e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=2.69508e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99062e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=1.19119e-04;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.736),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000258960.2:p.Glu148Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=4/12,cDNA_position=460,CDS_position=442,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=148,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000258960.2:c.442G>A
CDS|ENST00000258960	VCF	missense_variant	458	458	0.0	.	.	AC_Male=1;AF_NFE=8.96106e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-53;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06296e-06;Hom=0;AF_POPMAX=8.96106e-06;AN_POPMAX=111594;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41730e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.46809e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00924e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.932),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000258960.2:p.Pro149Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=4/12,cDNA_position=463,CDS_position=445,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=149,Codons=Ccc/Gcc,MINIMISED=1,HGVSc=ENST00000258960.2:c.445C>G
CDS|ENST00000258960	VCF	missense_variant	476	476	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-51;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06398e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41917e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=3.27293e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.08),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.369),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000258960.2:p.Gly155Ser,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=4/12,cDNA_position=481,CDS_position=463,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=155,Codons=Ggc/Agc,MINIMISED=1,HGVSc=ENST00000258960.2:c.463G>A
CDS|ENST00000258960	VCF	missense_variant	506	506	0.0	.	.	AC_Male=12;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|0|2|2|2|2|6|13|4|3|2|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.90310e-58;AF_OTH=5.47445e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=3;Hom_Male=0;AC=37;Hom_NFE=0;AF=1.50482e-04;Hom=0;AF_POPMAX=2.09150e-03;AN_POPMAX=15300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|3|2|6|4|8|3|1|3|0|1|1|1|0|2|0|1;AF_Male=8.91080e-05;AF_AFR=2.09150e-03;AC_raw=38;AB_MEDIAN=4.66288e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=2.24804e-04;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|36;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44169e-01;Hom_AMR=0;AC_EAS=0;AC_Female=25;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=32;AC_AFR=32;Hom_SAS=0;AC_ASJ=0;AF_raw=1.54302e-04;Hom_Female=0;AF_AMR=5.95841e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.66),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.0001983,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0.003,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=A:0.0010,Amino_acids=D/N,HGVSp=ENSP00000258960.2:p.Asp165Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.003,Allele=A,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=A:0.002214,cDNA_position=511,CDS_position=493,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs149737135,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=165,AA_MAF=A:0,Codons=Gat/Aat,MINIMISED=1,ExAC_AFR_MAF=A:1.977e-04,HGVSc=ENST00000258960.2:c.493G>A,ExAC_Adj_MAF=A:8.655e-05
CDS|ENST00000258960	VCF	missense_variant	509	509	0.0	.	.	AC_Male=0;AF_NFE=8.98101e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-44;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13524e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.33333e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=1.79863e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19608e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.264e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.503e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.206),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/C,HGVSp=ENSP00000258960.2:p.Arg166Cys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=T:0,cDNA_position=514,CDS_position=496,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778948844&COSM3518200,VARIANT_CLASS=SNV,Protein_position=166,Codons=Cgt/Tgt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.496C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	510	510	0.0	.	.	AC_Male=1;AF_NFE=1.79614e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-60;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13557e-06;Hom=0;AF_POPMAX=1.79614e-05;AN_POPMAX=111350;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.42721e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.70100e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=8.99329e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19786e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.264e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.503e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/P,HGVSp=ENSP00000258960.2:p.Arg166Pro,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=C:0,cDNA_position=515,CDS_position=497,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs748432196,VARIANT_CLASS=SNV,Protein_position=166,Codons=cGt/cCt,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.497G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	515	515	0.0	.	.	AC_Male=1;AF_NFE=2.69624e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-79;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22082e-05;Hom=0;AF_POPMAX=2.69624e-05;AN_POPMAX=111266;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43075e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.43709e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=51;AF_Female=1.79921e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.11),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.27e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.504e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.801),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=V/M,HGVSp=ENSP00000258960.2:p.Val168Met,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=4/12,ExAC_AMR_MAF=A:0,cDNA_position=520,CDS_position=502,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs773364852,VARIANT_CLASS=SNV,Protein_position=168,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.502G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	594	594	0.0	.	.	AC_Male=0;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-62;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=55;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99132e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.411),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/Q,HGVSp=ENSP00000258960.2:p.Pro194Gln,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=5/12,ExAC_AMR_MAF=T:0,cDNA_position=599,CDS_position=581,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,Protein_position=194,Codons=cCg/cAg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.581C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	594	594	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-188;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=145;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.99177e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.177),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000258960.2:p.Pro194Leu,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=5/12,ExAC_AMR_MAF=T:0,cDNA_position=599,CDS_position=581,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,Protein_position=194,Codons=cCg/cTg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.581C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	596	596	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-146;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.64198e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=162;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.16858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.638),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000258960.2:p.Glu195Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=5/12,cDNA_position=601,CDS_position=583,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=195,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000258960.2:c.583G>A
CDS|ENST00000258960	VCF	missense_variant	597	597	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-92;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=74;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.247),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/A,HGVSp=ENSP00000258960.2:p.Glu195Ala,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=5/12,cDNA_position=602,CDS_position=584,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=195,Codons=gAg/gCg,MINIMISED=1,HGVSc=ENST00000258960.2:c.584A>C
CDS|ENST00000258960	VCF	missense_variant	617	617	0.0	.	.	AC_Male=0;AF_NFE=8.96282e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-295;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06345e-06;Hom=0;AF_POPMAX=8.96282e-06;AN_POPMAX=111572;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51327e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=226;AF_Female=8.98763e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.243e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.96),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/W,HGVSp=ENSP00000258960.2:p.Arg202Trp,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=T:0,cDNA_position=622,CDS_position=604,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764148755,VARIANT_CLASS=SNV,Protein_position=202,Codons=Cgg/Tgg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.604C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	618	618	0.0	.	.	AC_Male=35;AF_NFE=1.07544e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|9|11|10|12|4|2|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-103;AF_OTH=1.82415e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=49;Hom_NFE=0;AF=1.99100e-04;Hom=0;AF_POPMAX=2.23441e-03;AN_POPMAX=9846;AC_NFE=12;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|4|3|1|2|1|6|7|4|4|0|2|1;AF_Male=2.59586e-04;AF_AFR=0.00000e+00;AC_raw=49;AB_MEDIAN=4.65116e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=2.23441e-03;DP_MEDIAN=74;AF_Female=1.25811e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|49;Hom_raw=0;AF_SAS=3.89838e-04;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=14;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=12;POPMAX=ASJ;AC_POPMAX=22;AC_AFR=0;Hom_SAS=0;AC_ASJ=22;AF_raw=1.98967e-04;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.85),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:0.0002225,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0002,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0002699,AFR_MAF=A:0.0005453,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.023),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/Q,HGVSp=ENSP00000258960.2:p.Arg202Gln,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=A:0,cDNA_position=623,CDS_position=605,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs150418753&COSM4067023,VARIANT_CLASS=SNV,Protein_position=202,Codons=cGg/cAg,MINIMISED=1,ExAC_AFR_MAF=A:2.224e-04,HGVSc=ENST00000258960.2:c.605G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	626	626	0.0	.	.	AC_Male=5;AF_NFE=1.25390e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|2|3|9|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-94;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=17;Hom_NFE=0;AF=6.90524e-05;Hom=0;AF_POPMAX=1.25390e-04;AN_POPMAX=111652;AC_NFE=14;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|0|1|1|1|2|0|2|2|0|1|0|1|0|0;AF_Male=3.70749e-05;AF_AFR=0.00000e+00;AC_raw=17;AB_MEDIAN=5.09033e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=64;AF_Female=1.07790e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|17;Hom_raw=0;AF_SAS=9.74596e-05;AS_RF=9.36765e-01;Hom_AMR=0;AC_EAS=0;AC_Female=12;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=NFE;AC_POPMAX=14;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.90294e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:5.768e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:7.495e-05,AFR_MAF=A:0.0001211,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.821),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000258960.2:p.Gly205Ser,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=A:0,cDNA_position=631,CDS_position=613,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs781499966,VARIANT_CLASS=SNV,Protein_position=205,Codons=Ggc/Agc,MINIMISED=1,ExAC_AFR_MAF=A:5.765e-05,HGVSc=ENST00000258960.2:c.613G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	631	631	0.0	.	.	AC_Male=1;AF_NFE=3.58230e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-225;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62467e-05;Hom=0;AF_POPMAX=3.58230e-05;AN_POPMAX=111660;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.41499e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55048e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=196;AF_Female=2.69440e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:3.296e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:5.996e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.281),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=W/C,HGVSp=ENSP00000258960.2:p.Trp206Cys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=T:0,cDNA_position=636,CDS_position=618,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs746041079,VARIANT_CLASS=SNV,Protein_position=206,Codons=tgG/tgT,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000258960.2:c.618G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	632	632	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-212;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06141e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.11392e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=158;AF_Female=8.98134e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08869e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.41),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.016),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000258960.2:p.Leu207Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=G:0,cDNA_position=637,CDS_position=619,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756018179,VARIANT_CLASS=SNV,Protein_position=207,Codons=Ctc/Gtc,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.619C>G,ExAC_Adj_MAF=G:8.639e-05
CDS|ENST00000258960	VCF	missense_variant	636	636	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|1|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-130;AF_OTH=1.82282e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03062e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|1|1|0|0|0|0;AF_Male=1.48278e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=76;AF_Female=2.69426e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.39678e-01;Hom_AMR=0;AC_EAS=4;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.43),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.043),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000258960.2:p.Pro208Leu,STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=A:0&T:0,cDNA_position=641,CDS_position=623,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,Protein_position=208,Codons=cCc/cTc,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000258960.2:c.623C>T,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000258960	VCF	missense_variant	636	636	0.0	.	.	AC_Male=1;AF_NFE=8.95415e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-239;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21837e-05;Hom=0;AF_POPMAX=5.95557e-05;AN_POPMAX=33582;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.31915e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=153;AF_Female=1.79617e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.48089e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.873),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/H,HGVSp=ENSP00000258960.2:p.Pro208His,STRAND=1,ExAC_SAS_MAF=A:0&T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=A:0&T:0,cDNA_position=641,CDS_position=623,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,Protein_position=208,Codons=cCc/cAc,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000258960.2:c.623C>A,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000258960	VCF	missense_variant	662	662	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-238;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.42254e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=142;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.49406e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.24),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.499e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000258960.2:p.Val217Leu,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=C:0,cDNA_position=667,CDS_position=649,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs774095582,VARIANT_CLASS=SNV,Protein_position=217,Codons=Gtc/Ctc,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.649G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	671	671	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-102;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.59375e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=7.94592e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.687),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/W,HGVSp=ENSP00000258960.2:p.Arg220Trp,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=6/12,cDNA_position=676,CDS_position=658,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=220,Codons=Cgg/Tgg,MINIMISED=1,HGVSc=ENST00000258960.2:c.658C>T
CDS|ENST00000258960	VCF	missense_variant	672	672	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-67;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21820e-05;Hom=0;AF_POPMAX=1.01523e-04;AN_POPMAX=9850;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.62963e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=1.01523e-04;DP_MEDIAN=51;AF_Female=1.79601e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.12),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.498e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/Q,HGVSp=ENSP00000258960.2:p.Arg220Gln,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=A:0,cDNA_position=677,CDS_position=659,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs771441667,VARIANT_CLASS=SNV,Protein_position=220,Codons=cGg/cAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.659G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	700	700	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-165;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95159e-06;AN_POPMAX=111712;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.56897e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=116;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17542e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.928),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=I/M,HGVSp=ENSP00000258960.2:p.Ile229Met,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,EA_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=G:0,cDNA_position=705,CDS_position=687,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs375089291,VARIANT_CLASS=SNV,Protein_position=229,Codons=atC/atG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.687C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	714	714	0.0	.	.	AC_Male=1;AF_NFE=1.79054e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-248;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12196e-06;Hom=0;AF_POPMAX=1.79054e-05;AN_POPMAX=111698;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41312e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.99184e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=192;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.647e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=H/R,HGVSp=ENSP00000258960.2:p.His234Arg,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=G:0,cDNA_position=719,CDS_position=701,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs775829411,VARIANT_CLASS=SNV,Protein_position=234,Codons=cAt/cGt,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.701A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	720	720	0.0	.	.	AC_Male=0;AF_NFE=8.95399e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-226;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06124e-06;Hom=0;AF_POPMAX=8.95399e-06;AN_POPMAX=111682;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.30168e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=179;AF_Female=8.98150e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.22854e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.96),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=Y/C,HGVSp=ENSP00000258960.2:p.Tyr236Cys,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=G:0,cDNA_position=725,CDS_position=707,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763238851,VARIANT_CLASS=SNV,Protein_position=236,Codons=tAt/tGt,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.707A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	726	726	0.0	.	.	AC_Male=0;AF_NFE=8.95592e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06167e-06;Hom=0;AF_POPMAX=8.95592e-06;AN_POPMAX=111658;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=8.98198e-06;GQ_HIST_ALT=0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.79803e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=T/K,HGVSp=ENSP00000258960.2:p.Thr238Lys,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=6/12,ExAC_AMR_MAF=A:0,cDNA_position=731,CDS_position=713,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764674925,VARIANT_CLASS=SNV,Protein_position=238,Codons=aCa/aAa,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.713C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	735	735	0.0	.	.	AC_Male=0;AF_NFE=8.97102e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-130;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06573e-06;Hom=0;AF_POPMAX=8.97102e-06;AN_POPMAX=111470;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.86905e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=168;AF_Female=8.98957e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.27e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.125),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=K/M,HGVSp=ENSP00000258960.2:p.Lys241Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=T:0,cDNA_position=740,CDS_position=722,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs758261924,VARIANT_CLASS=SNV,Protein_position=241,Codons=aAg/aTg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.722A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	737	737	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|3|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-55;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62617e-05;Hom=0;AF_POPMAX=1.19133e-04;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48449e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.74078e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=1.79775e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.92315e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=1.19133e-04;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.653e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.089),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/V,HGVSp=ENSP00000258960.2:p.Met242Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=G:0,cDNA_position=742,CDS_position=724,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs777621617,VARIANT_CLASS=SNV,Protein_position=242,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.724A>G,ExAC_Adj_MAF=G:0.0001728
CDS|ENST00000258960	VCF	missense_variant	777	777	0.0	.	.	AC_Male=1;AF_NFE=8.95319e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-214;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12216e-06;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41334e-06;AF_AFR=6.53424e-05;AC_raw=2;AB_MEDIAN=4.72222e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=180;AF_Female=8.98085e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.48607e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(1),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/H,HGVSp=ENSP00000258960.2:p.Arg255His,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=782,CDS_position=764,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746537411,VARIANT_CLASS=SNV,Protein_position=255,Codons=cGt/cAt,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000258960.2:c.764G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	794	794	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-66;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.42413e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.997),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000258960.2:p.Pro261Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=7/12,cDNA_position=799,CDS_position=781,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=261,Codons=Cca/Gca,MINIMISED=1,HGVSc=ENST00000258960.2:c.781C>G
CDS|ENST00000258960	VCF	missense_variant	839	839	0.0	.	.	AC_Male=2;AF_NFE=1.79067e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|2|0|0|1|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=3.98107e-153;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=1.34541e-04;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03059e-05;Hom=0;AF_POPMAX=1.34541e-04;AN_POPMAX=22298;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;AF_Male=1.48262e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.69880e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=2.69450e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.45888e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.2),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:4.119e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=G:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.076),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000258960.2:p.Ile276Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,EA_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=G:0,cDNA_position=844,CDS_position=826,ExAC_NFE_MAF=G:0.0004536,SYMBOL=NMT1,Existing_variation=rs371122860,VARIANT_CLASS=SNV,Protein_position=276,Codons=Atc/Gtc,MINIMISED=1,ExAC_AFR_MAF=G:4.118e-05,HGVSc=ENST00000258960.2:c.826A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	851	851	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-165;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06190e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.83051e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=118;AF_Female=8.98343e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53015e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.982),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/F,HGVSp=ENSP00000258960.2:p.Val280Phe,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=T:0,cDNA_position=856,CDS_position=838,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772467109,VARIANT_CLASS=SNV,Protein_position=280,Codons=Gtt/Ttt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.838G>T,ExAC_Adj_MAF=T:8.64e-05
CDS|ENST00000258960	VCF	missense_variant	860	860	0.0	.	.	AC_Male=1;AF_NFE=8.96266e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-105;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06312e-06;Hom=0;AF_POPMAX=8.96266e-06;AN_POPMAX=111574;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41587e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.93750e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=64;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.78341e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.793),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000258960.2:p.Ala283Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/12,cDNA_position=865,CDS_position=847,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=283,Codons=Gcc/Acc,MINIMISED=1,HGVSc=ENST00000258960.2:c.847G>A
CDS|ENST00000258960	VCF	missense_variant	864	864	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=6.30957e-128;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=4.48471e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06345e-06;Hom=0;AF_POPMAX=4.48471e-05;AN_POPMAX=22298;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41642e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.81013e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54228e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.24e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.988),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/E,HGVSp=ENSP00000258960.2:p.Gly284Glu,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=A:0,cDNA_position=869,CDS_position=851,ExAC_NFE_MAF=A:0.0001512,SYMBOL=NMT1,Existing_variation=rs766531390,VARIANT_CLASS=SNV,Protein_position=284,Codons=gGg/gAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.851G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	872	872	0.0	.	.	AC_Male=1;AF_NFE=1.79482e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-61;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21973e-05;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|1|0|0|0|0|1|1|0|0|0|0;AF_Male=7.42027e-06;AF_AFR=6.53424e-05;AC_raw=4;AB_MEDIAN=4.60242e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.79872e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.84998e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.0001212,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.428),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/I,HGVSp=ENSP00000258960.2:p.Leu287Ile,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=G:0,cDNA_position=877,CDS_position=859,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759663986,VARIANT_CLASS=SNV,Protein_position=287,Codons=Cta/Ata,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.859C>A,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	872	872	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-71;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21973e-05;Hom=0;AF_POPMAX=9.74659e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|1|1|0|0|0|0|0|0|0;AF_Male=2.22608e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.83333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=57;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=9.74659e-05;AS_RF=8.84998e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.0001212,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.55),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000258960.2:p.Leu287Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=G:0,cDNA_position=877,CDS_position=859,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759663986,VARIANT_CLASS=SNV,Protein_position=287,Codons=Cta/Gta,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.859C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	884	884	0.0	.	.	AC_Male=3;AF_NFE=2.70032e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|1|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-77;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.85053e-05;Hom=0;AF_POPMAX=1.96053e-04;AN_POPMAX=15302;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|1|0|1|0|1|0|1|1|1|1|0|0|0;AF_Male=2.22962e-05;AF_AFR=1.96053e-04;AC_raw=8;AB_MEDIAN=4.87441e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=3.60308e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51581e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=3;AC_AFR=3;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.35),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:3.303e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/I,HGVSp=ENSP00000258960.2:p.Val291Ile,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0002,Allele=A,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=A:0.000289,cDNA_position=889,CDS_position=871,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs376218058,VARIANT_CLASS=SNV,Protein_position=291,Codons=Gtt/Att,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000258960.2:c.871G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	888	888	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-153;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07382e-06;Hom=0;AF_POPMAX=2.97992e-05;AN_POPMAX=33558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.13889e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=72;AF_Female=9.01015e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92885e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.264e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.552),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/V,HGVSp=ENSP00000258960.2:p.Gly292Val,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=7/12,ExAC_AMR_MAF=T:0,cDNA_position=893,CDS_position=875,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764042790,VARIANT_CLASS=SNV,Protein_position=292,Codons=gGc/gTc,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.875G>T,ExAC_Adj_MAF=T:8.658e-05
CDS|ENST00000258960	VCF	missense_variant	923	923	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-132;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.94949e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.04140e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.927),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/W,HGVSp=ENSP00000258960.2:p.Arg304Trp,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=8/12,cDNA_position=928,CDS_position=910,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=304,Codons=Cgg/Tgg,MINIMISED=1,HGVSc=ENST00000258960.2:c.910C>T
CDS|ENST00000258960	VCF	missense_variant	966	966	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-79;AF_OTH=1.82349e-04;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06131e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.15730e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=8.98118e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.21292e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.625),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000258960.2:p.Met318Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=8/12,cDNA_position=971,CDS_position=953,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=318,Codons=aTg/aGg,MINIMISED=1,HGVSc=ENST00000258960.2:c.953T>G
CDS|ENST00000258960	VCF	missense_variant	984	984	0.0	.	.	AC_Male=1;AF_NFE=8.95672e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-104;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06187e-06;Hom=0;AF_POPMAX=8.95672e-06;AN_POPMAX=111648;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.41455e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.47059e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=85;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51581e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.024),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/R,HGVSp=ENSP00000258960.2:p.Met324Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=8/12,cDNA_position=989,CDS_position=971,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=324,Codons=aTg/aGg,MINIMISED=1,HGVSc=ENST00000258960.2:c.971T>G
CDS|ENST00000258960	VCF	missense_variant	995	995	0.0	.	.	AC_Male=1;AF_NFE=8.96523e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-50;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06385e-06;Hom=0;AF_POPMAX=8.96523e-06;AN_POPMAX=111542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41807e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=48;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.25808e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.68),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/G,HGVSp=ENSP00000258960.2:p.Arg328Gly,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=8/12,cDNA_position=1000,CDS_position=982,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=328,Codons=Cga/Gga,MINIMISED=1,HGVSc=ENST00000258960.2:c.982C>G
CDS|ENST00000258960	VCF	missense_variant	1001	1001	0.0	.	.	AC_Male=1;AF_NFE=8.96877e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-100;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06481e-06;Hom=0;AF_POPMAX=8.96877e-06;AN_POPMAX=111498;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.42005e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.02299e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=87;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18859e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.952),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/T,HGVSp=ENSP00000258960.2:p.Pro330Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=8/12,cDNA_position=1006,CDS_position=988,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=330,Codons=Cca/Aca,MINIMISED=1,HGVSc=ENST00000258960.2:c.988C>A
CDS|ENST00000258960	VCF	missense_variant	1007	1007	0.0	.	.	AC_Male=1;AF_NFE=1.80505e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-37;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.17702e-06;Hom=0;AF_POPMAX=1.80505e-05;AN_POPMAX=110800;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46614e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.08333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=9.03751e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.31706e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.9),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.253e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.649e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=T/A,HGVSp=ENSP00000258960.2:p.Thr332Ala,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=G:0,cDNA_position=1012,CDS_position=994,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767459640,VARIANT_CLASS=SNV,Protein_position=332,Codons=Act/Gct,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.994A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	1008	1008	0.0	.	.	AC_Male=1;AF_NFE=1.80470e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-36;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22639e-05;Hom=0;AF_POPMAX=2.98900e-05;AN_POPMAX=33456;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46480e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.21739e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=1.80737e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.04452e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=2.98900e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.77),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.193e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.64e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=T/S,HGVSp=ENSP00000258960.2:p.Thr332Ser,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=G:0,cDNA_position=1013,CDS_position=995,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750330678,VARIANT_CLASS=SNV,Protein_position=332,Codons=aCt/aGt,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.995C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	1008	1008	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=69;AB_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.99950e-05;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08797e-06;Hom=0;AF_POPMAX=5.80990e-05;AN_POPMAX=17212;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.57576e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=9.03685e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.47224e-02;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80990e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.43),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:9.193e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.64e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=T/N,HGVSp=ENSP00000258960.2:p.Thr332Asn,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=G:0,cDNA_position=1013,CDS_position=995,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750330678,VARIANT_CLASS=SNV,Protein_position=332,Codons=aCt/aAt,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.995C>A,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	1017	1017	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-50;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07515e-06;Hom=0;AF_POPMAX=6.54365e-05;AN_POPMAX=15282;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.54365e-05;AC_raw=1;AB_MEDIAN=5.14286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.01015e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.07823e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.114),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/I,HGVSp=ENSP00000258960.2:p.Thr335Ile,STRAND=1,CCDS=CCDS11494.1,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=9/12,cDNA_position=1022,CDS_position=1004,SYMBOL=NMT1,Existing_variation=rs375623297,VARIANT_CLASS=SNV,Protein_position=335,Codons=aCa/aTa,MINIMISED=1,HGVSc=ENST00000258960.2:c.1004C>T
CDS|ENST00000258960	VCF	missense_variant	1019	1019	0.0	.	.	AC_Male=2;AF_NFE=5.39035e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|1|0|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-36;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44328e-05;Hom=0;AF_POPMAX=5.39035e-05;AN_POPMAX=111310;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|2|0|0|0|2|1|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48683e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.59567e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=3.60172e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08070e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.06),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.734e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.116e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000258960.2:p.Ala336Thr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=A:0,cDNA_position=1024,CDS_position=1006,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs760138330,VARIANT_CLASS=SNV,Protein_position=336,Codons=Gct/Act,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000258960.2:c.1006G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1034	1034	0.0	.	.	AC_Male=2;AF_NFE=2.68846e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-62;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21914e-05;Hom=0;AF_POPMAX=2.68846e-05;AN_POPMAX=111588;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0|0;AF_Male=1.48381e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=8.98569e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44503e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.332e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.51e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.83),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/V,HGVSp=ENSP00000258960.2:p.Met341Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=G:0,cDNA_position=1039,CDS_position=1021,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs554809034,VARIANT_CLASS=SNV,Protein_position=341,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.1021A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	1052	1052	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-44;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06144e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.36055e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.07),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.059),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000258960.2:p.Pro347Ser,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/12,cDNA_position=1057,CDS_position=1039,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=347,Codons=Cca/Tca,HGVSc=ENST00000258960.2:c.1039C>T
CDS|ENST00000258960	VCF	missense_variant	1052	1052	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-78;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06144e-06;Hom=0;AF_POPMAX=2.97885e-05;AN_POPMAX=33570;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.09434e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=8.98182e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40992e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97885e-05;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.17),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000258960.2:p.Pro347Ala,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/12,cDNA_position=1057,CDS_position=1039,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=347,Codons=Cca/Gca,HGVSc=ENST00000258960.2:c.1039C>G
CDS|ENST00000258960	VCF	missense_variant	1055	1055	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-36;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12236e-06;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=1.48269e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.07246e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=8.81705e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.08),UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:1.651e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0.0001214,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000258960.2:p.Val348Leu,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=C:0,cDNA_position=1060,CDS_position=1042,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs753488937,VARIANT_CLASS=SNV,Protein_position=348,Codons=Gta/Cta,MINIMISED=1,ExAC_AFR_MAF=C:1.647e-05,HGVSc=ENST00000258960.2:c.1042G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	missense_variant	1061	1061	0.0	.	.	AC_Male=1;AF_NFE=8.95303e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-80;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06118e-06;Hom=0;AF_POPMAX=8.95303e-06;AN_POPMAX=111694;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.41334e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.74576e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=59;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50356e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.249e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.039),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=H/Y,HGVSp=ENSP00000258960.2:p.His350Tyr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=T:0,cDNA_position=1066,CDS_position=1048,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754671896,VARIANT_CLASS=SNV,Protein_position=350,Codons=Cac/Tac,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1048C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1067	1067	0.0	.	.	AC_Male=0;AF_NFE=1.79048e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-108;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12203e-06;Hom=0;AF_POPMAX=1.79048e-05;AN_POPMAX=111702;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.21263e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=1.79617e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.649e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:2.999e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.883),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/F,HGVSp=ENSP00000258960.2:p.Leu352Phe,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=T:0,cDNA_position=1072,CDS_position=1054,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778639871,VARIANT_CLASS=SNV,Protein_position=352,Codons=Ctc/Ttc,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.1054C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1077	1077	0.0	.	.	AC_Male=2;AF_NFE=3.58083e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|1|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-87;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03044e-05;Hom=0;AF_POPMAX=3.58083e-05;AN_POPMAX=111706;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|2|1|0|1|0|0;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=74;AF_Female=2.69416e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.179),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/M,HGVSp=ENSP00000258960.2:p.Arg355Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=T:0,cDNA_position=1082,CDS_position=1064,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757647993,VARIANT_CLASS=SNV,Protein_position=355,Codons=aGg/aTg,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000258960.2:c.1064G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1077	1077	0.0	.	.	AC_Male=1;AF_NFE=8.95207e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-75;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06088e-06;Hom=0;AF_POPMAX=8.95207e-06;AN_POPMAX=111706;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.10204e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=49;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.89),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=R/K,HGVSp=ENSP00000258960.2:p.Arg355Lys,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=T:0,cDNA_position=1082,CDS_position=1064,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757647993,VARIANT_CLASS=SNV,Protein_position=355,Codons=aGg/aAg,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000258960.2:c.1064G>A,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1084	1084	0.0	.	.	AC_Male=0;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-113;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=8.95159e-06;AN_POPMAX=111712;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.12195e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=82;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.737),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/F,HGVSp=ENSP00000258960.2:p.Leu357Phe,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=9/12,cDNA_position=1089,CDS_position=1071,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=357,Codons=ttG/ttC,MINIMISED=1,HGVSc=ENST00000258960.2:c.1071G>C
CDS|ENST00000258960	VCF	missense_variant	1101	1101	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.03025e-26;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12170e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=7.49951e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=1;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.95),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/M,HGVSp=ENSP00000258960.2:p.Thr363Met,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/12,cDNA_position=1106,CDS_position=1088,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=363,Codons=aCg/aTg,MINIMISED=1,HGVSc=ENST00000258960.2:c.1088C>T
CDS|ENST00000258960	VCF	missense_variant	1106	1106	0.0	.	.	AC_Male=18;AF_NFE=1.79035e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|5|11|3|6|4|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.31311e-75;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=32;Hom_NFE=0;AF=1.29949e-04;Hom=0;AF_POPMAX=1.89493e-03;AN_POPMAX=15304;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|2|4|2|4|0|1|2|0|1|0|2|0|3|0;AF_Male=1.33436e-04;AF_AFR=1.89493e-03;AC_raw=32;AB_MEDIAN=4.44496e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=68;AF_Female=1.25725e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|32;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44873e-01;Hom_AMR=0;AC_EAS=0;AC_Female=14;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=29;AC_AFR=29;Hom_SAS=0;AC_ASJ=0;AF_raw=1.29938e-04;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.29),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.0001401,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=A:0.0004,Amino_acids=V/I,HGVSp=ENSP00000258960.2:p.Val365Ile,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0014,Allele=A,IMPACT=MODERATE,EXON=9/12,ExAC_AMR_MAF=A:0.001538,cDNA_position=1111,CDS_position=1093,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs148483868,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=365,AA_MAF=A:0,Codons=Gtc/Atc,MINIMISED=1,ExAC_AFR_MAF=A:1.400e-04,HGVSc=ENST00000258960.2:c.1093G>A,ExAC_Adj_MAF=A:8.637e-05
CDS|ENST00000258960	VCF	missense_variant	1107	1107	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-74;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06088e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41301e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.61538e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=65;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.01512e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.3),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.02),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/D,HGVSp=ENSP00000258960.2:p.Val365Asp,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/12,cDNA_position=1112,CDS_position=1094,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=365,Codons=gTc/gAc,MINIMISED=1,HGVSc=ENST00000258960.2:c.1094T>A
CDS|ENST00000258960	VCF	missense_variant	1127	1127	0.0	.	.	AC_Male=1;AF_NFE=8.95223e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-19;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06128e-06;Hom=0;AF_POPMAX=8.95223e-06;AN_POPMAX=111704;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41400e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.13018e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.56),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.011),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000258960.2:p.Glu372Lys,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/12,cDNA_position=1132,CDS_position=1114,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=372,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000258960.2:c.1114G>A
CDS|ENST00000258960	VCF	missense_variant	1142	1142	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=2;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.86863e-01;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.25000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.71630e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.781),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000258960.2:p.Pro377Ser,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/12,cDNA_position=1147,CDS_position=1129,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=377,Codons=Ccc/Tcc,MINIMISED=1,HGVSc=ENST00000258960.2:c.1129C>T
CDS|ENST00000258960	VCF	missense_variant	1154	1154	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-82;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06342e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41774e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.13636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41631e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000258960.2:p.Ile381Val,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=9/12,cDNA_position=1159,CDS_position=1141,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=381,Codons=Atc/Gtc,MINIMISED=1,HGVSc=ENST00000258960.2:c.1141A>G
CDS|ENST00000258960	VCF	missense_variant	1160	1160	0.0	.	.	AC_Male=1;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-23;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06527e-06;Hom=0;AF_POPMAX=8.96379e-06;AN_POPMAX=111560;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42082e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.64592e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.15),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.07),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=D/N,HGVSp=ENSP00000258960.2:p.Asp383Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/12,cDNA_position=1165,CDS_position=1147,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=383,Codons=Gac/Aac,MINIMISED=1,HGVSc=ENST00000258960.2:c.1147G>A
CDS|ENST00000258960	VCF	missense_variant	1166	1166	0.0	.	.	AC_Male=0;AF_NFE=8.96716e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-48;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06646e-06;Hom=0;AF_POPMAX=8.96716e-06;AN_POPMAX=111518;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.63415e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=8.99313e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19983e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.907),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=F/I,HGVSp=ENSP00000258960.2:p.Phe385Ile,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=9/12,cDNA_position=1171,CDS_position=1153,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=385,Codons=Ttc/Atc,HGVSc=ENST00000258960.2:c.1153T>A
CDS|ENST00000258960	VCF	missense_variant	1166	1166	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=62;AB_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.57615e-03;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06646e-06;Hom=0;AF_POPMAX=5.79845e-05;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42291e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.44512e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.08515e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79845e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.749),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=F/L,HGVSp=ENSP00000258960.2:p.Phe385Leu,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=9/12,cDNA_position=1171,CDS_position=1153,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=385,Codons=Ttc/Ctc,HGVSc=ENST00000258960.2:c.1153T>C
CDS|ENST00000258960	VCF	missense_variant	1172	1172	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-27;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06967e-06;Hom=0;AF_POPMAX=3.25500e-05;AN_POPMAX=30722;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42810e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25500e-05;AS_RF=8.45900e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.172),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/L,HGVSp=ENSP00000258960.2:p.Val387Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=9/12,cDNA_position=1177,CDS_position=1159,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=387,Codons=Gtg/Ttg,MINIMISED=1,HGVSc=ENST00000258960.2:c.1159G>T
CDS|ENST00000258960	VCF	missense_variant	1177	1177	0.0	.	.	AC_Male=0;AF_NFE=8.99119e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-13;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07445e-06;Hom=0;AF_POPMAX=8.99119e-06;AN_POPMAX=111220;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=10;AF_Female=9.01242e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=5.86404e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.226),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=E/D,HGVSp=ENSP00000258960.2:p.Glu388Asp,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=9/12,cDNA_position=1182,CDS_position=1164,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=388,Codons=gaG/gaC,MINIMISED=1,HGVSc=ENST00000258960.2:c.1164G>C
CDS|ENST00000258960	VCF	missense_variant	1179	1179	0.0	.	.	AC_Male=1;AF_NFE=9.07935e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-136;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10806e-06;Hom=0;AF_POPMAX=9.07935e-06;AN_POPMAX=110140;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.50413e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57447e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06919e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.73),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=N/S,HGVSp=ENSP00000258960.2:p.Asn389Ser,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/12,cDNA_position=1184,CDS_position=1166,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=389,Codons=aAc/aGc,MINIMISED=1,HGVSc=ENST00000258960.2:c.1166A>G
CDS|ENST00000258960	VCF	missense_variant	1181	1181	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-88;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10590e-06;Hom=0;AF_POPMAX=3.28947e-05;AN_POPMAX=30400;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.49895e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.91803e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.28947e-05;AS_RF=9.51545e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.41),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.487e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000258960.2:p.Ala390Thr,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1186,CDS_position=1168,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749387380,VARIANT_CLASS=SNV,Protein_position=390,Codons=Gca/Aca,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1168G>A,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1181	1181	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-224;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10590e-06;Hom=0;AF_POPMAX=3.28947e-05;AN_POPMAX=30400;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.26136e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=176;AF_Female=9.07441e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.28947e-05;AS_RF=9.51545e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated(0.94),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.487e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/S,HGVSp=ENSP00000258960.2:p.Ala390Ser,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1186,CDS_position=1168,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749387380,VARIANT_CLASS=SNV,Protein_position=390,Codons=Gca/Tca,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1168G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1182	1182	0.0	.	.	AC_Male=1;AF_NFE=9.06208e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-28;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09954e-06;Hom=0;AF_POPMAX=9.06208e-06;AN_POPMAX=110350;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48783e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.29412e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.41699e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.23),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000258960.2:p.Ala390Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/12,cDNA_position=1187,CDS_position=1169,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=390,Codons=gCa/gTa,MINIMISED=1,HGVSc=ENST00000258960.2:c.1169C>T
CDS|ENST00000258960	VCF	missense_variant	1187	1187	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97631e-198;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63556e-05;Hom=0;AF_POPMAX=1.30881e-04;AN_POPMAX=30562;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.49365e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55398e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=170;AF_Female=1.80727e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=1.30881e-04;AS_RF=9.08567e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=4;POPMAX=SAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:3.362e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0002704,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.643),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/R,HGVSp=ENSP00000258960.2:p.Gly392Arg,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1192,CDS_position=1174,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs779143534&COSM1217528,VARIANT_CLASS=SNV,Protein_position=392,Codons=Gga/Aga,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000258960.2:c.1174G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1190	1190	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-80;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08320e-06;Hom=0;AF_POPMAX=1.02333e-04;AN_POPMAX=9772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=7.35294e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.02333e-04;DP_MEDIAN=34;AF_Female=9.02266e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.21409e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.375e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.51e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000258960.2:p.Glu393Lys,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1195,CDS_position=1177,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs748344051,VARIANT_CLASS=SNV,Protein_position=393,Codons=Gag/Aag,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.1177G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1218	1218	0.0	.	.	AC_Male=1;AF_NFE=1.79724e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|0|0|0|0|0|2|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-33;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22190e-05;Hom=0;AF_POPMAX=5.80316e-05;AN_POPMAX=17232;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43572e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.33761e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=1.80125e-05;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20100e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80316e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:8.256e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.761),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/M,HGVSp=ENSP00000258960.2:p.Thr402Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1223,CDS_position=1205,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs773052955&COSM1679874,VARIANT_CLASS=SNV,Protein_position=402,Codons=aCg/aTg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1205C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1232	1232	0.0	.	.	AC_Male=1;AF_NFE=8.95560e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06164e-06;Hom=0;AF_POPMAX=8.95560e-06;AN_POPMAX=111662;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41444e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.94824e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=483;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40352e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.241e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.5e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.021),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000258960.2:p.Ile407Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=G:0,cDNA_position=1237,CDS_position=1219,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs770912575,VARIANT_CLASS=SNV,Protein_position=407,Codons=Atc/Gtc,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.1219A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	1248	1248	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-304;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.47876e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=259;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.21770e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.56),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.238e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/N,HGVSp=ENSP00000258960.2:p.Thr412Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1253,CDS_position=1235,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs776660504,VARIANT_CLASS=SNV,Protein_position=412,Codons=aCc/aAc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.1235C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1257	1257	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-112;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.12903e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=62;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.83306e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=S/N,HGVSp=ENSP00000258960.2:p.Ser415Asn,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/12,cDNA_position=1262,CDS_position=1244,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=415,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000258960.2:c.1244G>A
CDS|ENST00000258960	VCF	missense_variant	1284	1284	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06058e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41235e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.93082e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=318;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36790e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.236e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.092),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000258960.2:p.Asn424Ser,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=G:0,cDNA_position=1289,CDS_position=1271,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs775334053,VARIANT_CLASS=SNV,Protein_position=424,Codons=aAc/aGc,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.1271A>G,ExAC_Adj_MAF=G:8.637e-05
CDS|ENST00000258960	VCF	missense_variant	1286	1286	0.0	.	.	AC_Male=0;AF_NFE=4.47571e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|4|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-115;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84248e-05;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|3|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=9;AB_MEDIAN=4.67391e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=91;AF_Female=6.28603e-05;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=1;AF_SAS=0.00000e+00;AS_RF=9.08698e-01;Hom_AMR=0;AC_EAS=1;AC_Female=7;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.65450e-05;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.18),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:1.647e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.072),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=V/I,HGVSp=ENSP00000258960.2:p.Val425Ile,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1291,CDS_position=1273,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767839828,VARIANT_CLASS=SNV,Protein_position=425,Codons=Gtt/Att,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000258960.2:c.1273G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1318	1318	0.0	.	.	AC_Male=11;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|8|4|11|4|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-90;AF_OTH=1.45826e-03;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=8;Hom_Male=0;AC=29;Hom_NFE=0;AF=1.17774e-04;Hom=1;AF_POPMAX=5.95557e-04;AN_POPMAX=33582;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=1;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|2|2|1|5|3|1|0|1|0;AF_Male=8.15407e-05;AF_AFR=0.00000e+00;AC_raw=29;AB_MEDIAN=4.58333e-01;Hom_EAS=0;AC_AMR=20;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=1.61679e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|28;Hom_raw=1;AF_SAS=0.00000e+00;AS_RF=9.54732e-01;Hom_AMR=0;AC_EAS=0;AC_Female=18;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=20;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.17756e-04;Hom_Female=1;AF_AMR=5.95557e-04;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.17),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:0.0001483,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:7.492e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.074),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/I,HGVSp=ENSP00000258960.2:p.Met435Ile,STRAND=1,ExAC_SAS_MAF=T:0.001101,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=T:0,cDNA_position=1323,CDS_position=1305,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs750807200,VARIANT_CLASS=SNV,Protein_position=435,Codons=atG/atT,MINIMISED=1,ExAC_AFR_MAF=T:1.483e-04,HGVSc=ENST00000258960.2:c.1305G>T,ExAC_Adj_MAF=T:0.001036
CDS|ENST00000258960	VCF	missense_variant	1322	1322	0.0	.	.	AC_Male=1;AF_NFE=8.95207e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06161e-06;Hom=0;AF_POPMAX=8.95207e-06;AN_POPMAX=111706;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41345e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.25597e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=293;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.498e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.977),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=D/N,HGVSp=ENSP00000258960.2:p.Asp437Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1327,CDS_position=1309,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs766935430,VARIANT_CLASS=SNV,Protein_position=437,Codons=Gac/Aac,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.1309G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1325	1325	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-104;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06187e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.88636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=88;AF_Female=8.98424e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.14239e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.1),UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.699),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000258960.2:p.Ala438Thr,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=10/12,ExAC_AMR_MAF=A:0,cDNA_position=1330,CDS_position=1312,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs755095071&COSM4067024,VARIANT_CLASS=SNV,Protein_position=438,Codons=Gcc/Acc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.1312G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1337	1337	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50468e-04;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06587e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.78711e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.99507e-06;GQ_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44500e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.972),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000258960.2:p.Ala442Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=10/12,cDNA_position=1342,CDS_position=1324,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=442,Codons=Gcc/Acc,MINIMISED=1,HGVSc=ENST00000258960.2:c.1324G>A
CDS|ENST00000258960	VCF	missense_variant	1365	1365	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-103;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06062e-06;Hom=0;AF_POPMAX=1.01523e-04;AN_POPMAX=9850;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.31818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.01523e-04;DP_MEDIAN=88;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50356e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.935),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=N/S,HGVSp=ENSP00000258960.2:p.Asn451Ser,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/12,cDNA_position=1370,CDS_position=1352,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=451,Codons=aAt/aGt,MINIMISED=1,HGVSc=ENST00000258960.2:c.1352A>G
CDS|ENST00000258960	VCF	missense_variant	1367	1367	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-151;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=108;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43418e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.927),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/T,HGVSp=ENSP00000258960.2:p.Ala452Thr,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/12,cDNA_position=1372,CDS_position=1354,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=452,Codons=Gca/Aca,MINIMISED=1,HGVSc=ENST00000258960.2:c.1354G>A
CDS|ENST00000258960	VCF	missense_variant	1388	1388	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-121;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.56311e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.26486e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.45),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.016),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=K/E,HGVSp=ENSP00000258960.2:p.Lys459Glu,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/12,cDNA_position=1393,CDS_position=1375,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=459,Codons=Aaa/Gaa,MINIMISED=1,HGVSc=ENST00000258960.2:c.1375A>G
CDS|ENST00000258960	VCF	missense_variant	1392	1392	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-44;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.63636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.14571e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.24),UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=T/N,HGVSp=ENSP00000258960.2:p.Thr460Asn,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/12,ExAC_AMR_MAF=A:0,cDNA_position=1397,CDS_position=1379,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs772801108,VARIANT_CLASS=SNV,Protein_position=460,Codons=aCc/aAc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.1379C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	missense_variant	1397	1397	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-140;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=6.53509e-05;AN_POPMAX=15302;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41246e-06;AF_AFR=6.53509e-05;AC_raw=1;AB_MEDIAN=5.10638e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=94;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.98),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/M,HGVSp=ENSP00000258960.2:p.Leu462Met,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,EA_MAF=T:0,Allele=A,IMPACT=MODERATE,EXON=11/12,ExAC_AMR_MAF=T:0,cDNA_position=1402,CDS_position=1384,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs141629884,VARIANT_CLASS=SNV,Protein_position=462,Codons=Ctg/Atg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.1384C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	missense_variant	1418	1418	0.0	.	.	AC_Male=10;AF_NFE=9.84622e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|2|7|4|0|1|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-84;AF_OTH=3.64564e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=18;Hom_NFE=0;AF=7.30917e-05;Hom=0;AF_POPMAX=1.48889e-04;AN_POPMAX=33582;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|1|1|1|1|1|0|1|1|0|1|1|1;AF_Male=7.41246e-05;AF_AFR=0.00000e+00;AC_raw=18;AB_MEDIAN=4.35440e-01;Hom_EAS=0;AC_AMR=5;AF_ASJ=0.00000e+00;DP_MEDIAN=80;AF_Female=7.18404e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|18;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44331e-01;Hom_AMR=0;AC_EAS=0;AC_Female=8;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=7.30899e-05;Hom_Female=0;AF_AMR=1.48889e-04;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.19),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:4.943e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:7.495e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000258960.2:p.Ile469Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/12,ExAC_AMR_MAF=G:0,cDNA_position=1423,CDS_position=1405,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774301899,VARIANT_CLASS=SNV,Protein_position=469,Codons=Ata/Gta,MINIMISED=1,ExAC_AFR_MAF=G:4.942e-05,HGVSc=ENST00000258960.2:c.1405A>G,ExAC_Adj_MAF=G:8.642e-05
CDS|ENST00000258960	VCF	missense_variant	1427	1427	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-262;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=1.01543e-04;AN_POPMAX=9848;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57547e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.01543e-04;DP_MEDIAN=212;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.98494e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&PROSITE_patterns:PS00976&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.977),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/S,HGVSp=ENSP00000258960.2:p.Gly472Ser,STRAND=1,CCDS=CCDS11494.1,Allele=A,IMPACT=MODERATE,EXON=11/12,cDNA_position=1432,CDS_position=1414,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=472,Codons=Ggc/Agc,MINIMISED=1,HGVSc=ENST00000258960.2:c.1414G>A
CDS|ENST00000258960	VCF	missense_variant	1469	1469	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-133;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06114e-06;Hom=0;AF_POPMAX=2.97796e-05;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0;AF_Male=7.41323e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.33333e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=90;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.15969e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.36),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.023),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=M/L,HGVSp=ENSP00000258960.2:p.Met486Leu,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=11/12,cDNA_position=1474,CDS_position=1456,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=486,Codons=Atg/Ttg,MINIMISED=1,HGVSc=ENST00000258960.2:c.1456A>T
CDS|ENST00000258960	VCF	missense_variant	1473	1473	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-120;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06167e-06;Hom=0;AF_POPMAX=2.97796e-05;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41367e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.81481e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=108;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.53),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=G/A,HGVSp=ENSP00000258960.2:p.Gly487Ala,STRAND=1,CCDS=CCDS11494.1,Allele=C,IMPACT=MODERATE,EXON=11/12,cDNA_position=1478,CDS_position=1460,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=487,Codons=gGg/gCg,MINIMISED=1,HGVSc=ENST00000258960.2:c.1460G>C
CDS|ENST00000258960	VCF	missense_variant	1476	1476	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-220;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06197e-06;Hom=0;AF_POPMAX=2.97796e-05;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.64417e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=163;AF_Female=8.98376e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50841e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97796e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.095),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=A/V,HGVSp=ENSP00000258960.2:p.Ala488Val,STRAND=1,CCDS=CCDS11494.1,Allele=T,IMPACT=MODERATE,EXON=11/12,cDNA_position=1481,CDS_position=1463,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=488,Codons=gCa/gTa,MINIMISED=1,HGVSc=ENST00000258960.2:c.1463C>T
CDS|ENST00000258960	VCF	missense_variant	1479	1479	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-187;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06177e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.68807e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=109;AF_Female=8.98279e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.40367e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.12),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.248e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=G:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,EAS_MAF=G:0,EUR_MAF=G:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.008),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,GMAF=G:0.0002,Amino_acids=E/G,HGVSp=ENSP00000258960.2:p.Glu489Gly,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/12,ExAC_AMR_MAF=G:0,cDNA_position=1484,CDS_position=1466,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs578117787,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=489,AA_MAF=G:0.001,Codons=gAg/gGg,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000258960.2:c.1466A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	1481	1481	0.0	.	.	AC_Male=1;AF_NFE=1.79115e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-88;AF_OTH=1.82482e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21862e-05;Hom=0;AF_POPMAX=1.79115e-05;AN_POPMAX=111660;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|1|0;AF_Male=7.41444e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=62;AF_Female=1.79682e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51743e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.5),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.65e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.001e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.102),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=K/E,HGVSp=ENSP00000258960.2:p.Lys490Glu,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/12,ExAC_AMR_MAF=G:0,cDNA_position=1486,CDS_position=1468,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs766069961,VARIANT_CLASS=SNV,Protein_position=490,Codons=Aag/Gag,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.1468A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	missense_variant	1482	1482	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-127;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06220e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=7.41444e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.34091e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=88;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.05),UNIPARC=UPI0000130275,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.152),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,Consequence=missense_variant&splice_region_variant,Amino_acids=K/R,HGVSp=ENSP00000258960.2:p.Lys490Arg,STRAND=1,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=11/12,cDNA_position=1487,CDS_position=1469,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=490,Codons=aAg/aGg,MINIMISED=1,HGVSc=ENST00000258960.2:c.1469A>G
CDS|ENST00000258960	VCF	missense_variant	1490	1490	0.0	.	.	AC_Male=1;AF_NFE=1.79263e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.76188e-107;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14180e-06;Hom=0;AF_POPMAX=1.79263e-05;AN_POPMAX=111568;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AF_Male=7.42732e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.90799e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=9.00836e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96721e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.437),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=missense_variant,Amino_acids=L/V,HGVSp=ENSP00000258960.2:p.Leu493Val,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODERATE,EXON=12/12,ExAC_AMR_MAF=G:0,cDNA_position=1495,CDS_position=1477,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs765115917,VARIANT_CLASS=SNV,Protein_position=493,Codons=Ctg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.1477C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	dbSNP	sequence_variant	1	1	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs749106795;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3	3	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs768521050;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4	4	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1345027263;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	8	8	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs892415557;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	9	9	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs774460908;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	11	11	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs748067291;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	13	13	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1346180677;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	18	18	0.0	+	.	consequence_type=missense_variant;id=rs771527303;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	20	20	0.0	+	.	consequence_type=missense_variant;id=rs772761859;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	21	21	0.0	+	.	consequence_type=missense_variant;id=rs1317068708;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	23	23	0.0	+	.	consequence_type=missense_variant;id=rs983223652;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	24	24	0.0	+	.	consequence_type=missense_variant;id=rs760309598;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	26	26	0.0	+	.	consequence_type=missense_variant;id=rs564172691;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	27	27	0.0	+	.	consequence_type=missense_variant;id=rs1314954450;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	28	28	0.0	+	.	consequence_type=synonymous_variant;id=rs1009445042;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	29	29	0.0	+	.	consequence_type=missense_variant;id=rs267604914;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	31	31	0.0	+	.	consequence_type=synonymous_variant;id=rs776210749;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	32	32	0.0	+	.	consequence_type=missense_variant;id=rs1292079143;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	33	33	0.0	+	.	consequence_type=missense_variant;id=rs1022554088;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	34	34	0.0	+	.	consequence_type=synonymous_variant;id=rs763334167;alleles=A%2CC%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	35	35	0.0	+	.	consequence_type=missense_variant;id=rs907713546;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	36	36	0.0	+	.	consequence_type=missense_variant;id=rs764406772;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	37	37	0.0	+	.	consequence_type=synonymous_variant;id=rs1253429311;alleles=A%2CC%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	38	38	0.0	+	.	consequence_type=missense_variant;id=rs752105945;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	43	43	0.0	+	.	consequence_type=synonymous_variant;id=rs757761311;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	44	44	0.0	+	.	consequence_type=missense_variant;id=rs767553043;alleles=C%2CA%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	45	45	0.0	+	.	consequence_type=missense_variant;id=rs750513385;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	46	46	0.0	+	.	consequence_type=synonymous_variant;id=rs1007666082;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	47	62	0.0	+	.	consequence_type=frameshift_variant;id=rs1306813664;alleles=CCGGCACCTCCGCTGC%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	63	63	0.0	+	.	consequence_type=missense_variant;id=rs937347334;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	67	67	0.0	+	.	consequence_type=synonymous_variant;id=rs1229832497;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	69	69	0.0	+	.	consequence_type=missense_variant;id=rs1315229471;alleles=T%2CC%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	72	72	0.0	+	.	consequence_type=missense_variant;id=rs772952636;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	76	77	0.0	+	.	consequence_type=inframe_insertion;id=rs1219870401;alleles=-%2CGGGAAC
CDS|ENST00000258960	dbSNP	sequence_variant	83	83	0.0	+	.	consequence_type=missense_variant;id=rs746539074;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	84	84	0.0	+	.	consequence_type=missense_variant;id=rs1437942507;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	86	87	0.0	+	.	consequence_type=inframe_insertion;id=rs763191382;alleles=-%2CACGGCC
CDS|ENST00000258960	dbSNP	sequence_variant	89	89	0.0	+	.	consequence_type=missense_variant;id=rs770300796;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	90	90	0.0	+	.	consequence_type=missense_variant;id=rs1451260585;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	93	93	0.0	+	.	consequence_type=missense_variant;id=rs1362841019;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	94	94	0.0	+	.	consequence_type=missense_variant;id=rs776300314;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	95	95	0.0	+	.	consequence_type=missense_variant;id=rs1159616651;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	96	96	0.0	+	.	consequence_type=missense_variant;id=rs1185809906;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	100	100	0.0	+	.	consequence_type=missense_variant;id=rs759161485;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	102	102	0.0	+	.	consequence_type=missense_variant;id=rs764495116;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	104	104	0.0	+	.	consequence_type=missense_variant;id=rs774684452;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	107	107	0.0	+	.	consequence_type=missense_variant;id=rs976121906;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	111	111	0.0	+	.	consequence_type=missense_variant;id=rs895881728;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	112	112	0.0	+	.	consequence_type=missense_variant;id=rs762294220;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	115	115	0.0	+	.	consequence_type=synonymous_variant;id=rs768076232;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	124	124	0.0	+	.	consequence_type=synonymous_variant;id=rs1328029981;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	133	133	0.0	+	.	consequence_type=missense_variant;id=rs750844557;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	135	135	0.0	+	.	consequence_type=missense_variant;id=rs756247053;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	137	139	0.0	+	.	consequence_type=inframe_deletion;id=rs375981533;alleles=AAC%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	141	141	0.0	+	.	consequence_type=missense_variant;id=rs1271597368;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	142	142	0.0	+	.	consequence_type=splice_region_variant;id=rs143955814;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	147	147	0.0	+	.	consequence_type=missense_variant;id=rs752810524;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	149	149	0.0	+	.	consequence_type=missense_variant;id=rs758247752;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	150	150	0.0	+	.	consequence_type=missense_variant;id=rs1199096532;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	153	153	0.0	+	.	consequence_type=missense_variant;id=rs1286861992;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	154	154	0.0	+	.	consequence_type=synonymous_variant;id=rs777402320;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	155	155	0.0	+	.	consequence_type=missense_variant;id=rs1192808116;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	156	156	0.0	+	.	consequence_type=missense_variant;id=rs1212522731;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	161	161	0.0	+	.	consequence_type=missense_variant;id=rs140455291;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	162	162	0.0	+	.	consequence_type=missense_variant;id=rs757177482;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	174	174	0.0	+	.	consequence_type=missense_variant;id=rs780748535;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	177	177	0.0	+	.	consequence_type=missense_variant;id=rs774451911;alleles=A%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	189	189	0.0	+	.	consequence_type=missense_variant;id=rs1468231466;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	194	194	0.0	+	.	consequence_type=missense_variant;id=rs3087878;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	199	199	0.0	+	.	consequence_type=synonymous_variant;id=rs375158125;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	204	204	0.0	+	.	consequence_type=missense_variant;id=rs201559014;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	206	206	0.0	+	.	consequence_type=missense_variant;id=rs779784731;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	214	214	0.0	+	.	consequence_type=synonymous_variant;id=rs141656657;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	216	216	0.0	+	.	consequence_type=missense_variant;id=rs1399730029;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	217	217	0.0	+	.	consequence_type=synonymous_variant;id=rs1315823029;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	223	223	0.0	+	.	consequence_type=synonymous_variant;id=rs369434915;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	233	233	0.0	+	.	consequence_type=missense_variant;id=rs1405046109;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	234	234	0.0	+	.	consequence_type=missense_variant;id=rs1284414737;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	235	235	0.0	+	.	consequence_type=synonymous_variant;id=rs184508172;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	238	238	0.0	+	.	consequence_type=missense_variant;id=rs1231776580;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	242	242	0.0	+	.	consequence_type=missense_variant;id=rs1281614790;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	248	248	0.0	+	.	consequence_type=missense_variant;id=rs761306458;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	254	254	0.0	+	.	consequence_type=start_lost;id=rs767459577;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	258	258	0.0	+	.	consequence_type=missense_variant;id=rs367954716;alleles=A%2CC%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	262	262	0.0	+	.	consequence_type=synonymous_variant;id=rs200633656;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	265	265	0.0	+	.	consequence_type=missense_variant;id=rs1018863986;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	274	274	0.0	+	.	consequence_type=missense_variant;id=rs1051019368;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	280	280	0.0	+	.	consequence_type=missense_variant;id=rs779405921;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	286	286	0.0	+	.	consequence_type=synonymous_variant;id=rs1382805858;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	299	299	0.0	+	.	consequence_type=missense_variant;id=rs1463089836;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	300	300	0.0	+	.	consequence_type=missense_variant;id=rs1308984921;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	301	301	0.0	+	.	consequence_type=synonymous_variant;id=rs372318247;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	307	307	0.0	+	.	consequence_type=synonymous_variant;id=rs754577624;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	313	313	0.0	+	.	consequence_type=synonymous_variant;id=rs1391388443;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	315	315	0.0	+	.	consequence_type=missense_variant;id=rs778561485;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	317	317	0.0	+	.	consequence_type=missense_variant;id=rs747390700;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	321	321	0.0	+	.	consequence_type=missense_variant;id=rs1335366133;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	322	322	0.0	+	.	consequence_type=missense_variant;id=rs771371139;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	323	323	0.0	+	.	consequence_type=missense_variant;id=rs563736659;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	325	325	0.0	+	.	consequence_type=synonymous_variant;id=rs746348189;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	326	326	0.0	+	.	consequence_type=missense_variant;id=rs1294041634;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	327	327	0.0	+	.	consequence_type=missense_variant;id=rs1416691571;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	329	329	0.0	+	.	consequence_type=missense_variant;id=rs868718436;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	331	331	0.0	+	.	consequence_type=synonymous_variant;id=rs1229714849;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	338	338	0.0	+	.	consequence_type=missense_variant;id=rs1348860194;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	339	339	0.0	+	.	consequence_type=missense_variant;id=rs770043528;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	345	345	0.0	+	.	consequence_type=missense_variant;id=rs775419569;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	346	346	0.0	+	.	consequence_type=synonymous_variant;id=rs972147914;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	347	347	0.0	+	.	consequence_type=missense_variant;id=rs1297768336;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	348	348	0.0	+	.	consequence_type=missense_variant;id=rs1443418786;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	349	349	0.0	+	.	consequence_type=synonymous_variant;id=rs1338651806;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	350	350	0.0	+	.	consequence_type=missense_variant;id=rs1196722115;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	352	352	0.0	+	.	consequence_type=synonymous_variant;id=rs1244710451;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	357	357	0.0	+	.	consequence_type=missense_variant;id=rs377156745;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	359	359	0.0	+	.	consequence_type=missense_variant;id=rs1182546534;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	366	366	0.0	+	.	consequence_type=missense_variant;id=rs1391284036;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	370	370	0.0	+	.	consequence_type=synonymous_variant;id=rs1253657974;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	378	378	0.0	+	.	consequence_type=missense_variant;id=rs764230766;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	379	379	0.0	+	.	consequence_type=synonymous_variant;id=rs1170526700;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	385	385	0.0	+	.	consequence_type=synonymous_variant;id=rs774578466;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	386	386	0.0	+	.	consequence_type=missense_variant;id=rs761622308;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	391	391	0.0	+	.	consequence_type=synonymous_variant;id=rs767261647;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	393	393	0.0	+	.	consequence_type=missense_variant;id=rs144433221;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	400	400	0.0	+	.	consequence_type=splice_region_variant;id=rs199678185;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	405	405	0.0	+	.	consequence_type=missense_variant;id=rs1216003679;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	412	412	0.0	+	.	consequence_type=synonymous_variant;id=rs760391896;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	415	415	0.0	+	.	consequence_type=synonymous_variant;id=rs766241230;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	416	416	0.0	+	.	consequence_type=missense_variant;id=rs753759265;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	421	421	0.0	+	.	consequence_type=synonymous_variant;id=rs1269052802;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	424	424	0.0	+	.	consequence_type=synonymous_variant;id=rs147841016;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	425	425	0.0	+	.	consequence_type=missense_variant;id=rs752448187;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	430	430	0.0	+	.	consequence_type=synonymous_variant;id=rs1250252141;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	431	431	0.0	+	.	consequence_type=missense_variant;id=rs758111913;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	432	432	0.0	+	.	consequence_type=missense_variant;id=rs1421268751;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	434	434	0.0	+	.	consequence_type=missense_variant;id=rs201386803;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	436	436	0.0	+	.	consequence_type=synonymous_variant;id=rs535242567;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	437	437	0.0	+	.	consequence_type=missense_variant;id=rs986408291;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	439	439	0.0	+	.	consequence_type=synonymous_variant;id=rs1418173661;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	450	450	0.0	+	.	consequence_type=missense_variant;id=rs955288678;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	451	451	0.0	+	.	consequence_type=synonymous_variant;id=rs1456376961;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	452	452	0.0	+	.	consequence_type=missense_variant;id=rs1161073719;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	455	455	0.0	+	.	consequence_type=missense_variant;id=rs1305018160;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	457	457	0.0	+	.	consequence_type=synonymous_variant;id=rs910463482;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	458	458	0.0	+	.	consequence_type=missense_variant;id=rs1366323829;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	473	473	0.0	+	.	consequence_type=stop_gained;id=rs1435626124;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	476	476	0.0	+	.	consequence_type=missense_variant;id=rs1291739811;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	484	484	0.0	+	.	consequence_type=synonymous_variant;id=rs559376009;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	494	494	0.0	+	.	consequence_type=synonymous_variant;id=rs1199425750;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	500	500	0.0	+	.	consequence_type=synonymous_variant;id=rs1132898;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	502	502	0.0	+	.	consequence_type=synonymous_variant;id=rs1306112590;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	505	505	0.0	+	.	consequence_type=synonymous_variant;id=rs749766632;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	506	506	0.0	+	.	consequence_type=missense_variant;id=rs149737135;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	509	509	0.0	+	.	consequence_type=missense_variant;id=rs778948844;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	510	510	0.0	+	.	consequence_type=missense_variant;id=rs748432196;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	511	511	0.0	+	.	consequence_type=synonymous_variant;id=rs1221407945;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	512	512	0.0	+	.	consequence_type=missense_variant;id=rs1269207571;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	514	514	0.0	+	.	consequence_type=synonymous_variant;id=rs772281237;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	515	515	0.0	+	.	consequence_type=missense_variant;id=rs773364852;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	527	527	0.0	+	.	consequence_type=missense_variant;id=rs1377176181;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	535	535	0.0	+	.	consequence_type=missense_variant;id=rs770678984;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	541	541	0.0	+	.	consequence_type=missense_variant;id=rs927057705;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	553	553	0.0	+	.	consequence_type=synonymous_variant;id=rs151247418;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	568	568	0.0	+	.	consequence_type=synonymous_variant;id=rs776474941;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	571	571	0.0	+	.	consequence_type=synonymous_variant;id=rs1410437263;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	572	572	0.0	+	.	consequence_type=missense_variant;id=rs1283407561;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	583	583	0.0	+	.	consequence_type=synonymous_variant;id=rs759459614;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	592	592	0.0	+	.	consequence_type=synonymous_variant;id=rs372926712;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	594	594	0.0	+	.	consequence_type=missense_variant;id=rs775510228;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	595	595	0.0	+	.	consequence_type=synonymous_variant;id=rs146345914;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	596	596	0.0	+	.	consequence_type=missense_variant;id=rs1339503876;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	597	597	0.0	+	.	consequence_type=missense_variant;id=rs1445433341;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	598	598	0.0	+	.	consequence_type=missense_variant;id=rs866488889;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	599	599	0.0	+	.	consequence_type=missense_variant;id=rs1311826897;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	605	605	0.0	+	.	consequence_type=synonymous_variant;id=rs1259891285;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	617	617	0.0	+	.	consequence_type=missense_variant;id=rs764148755;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	618	618	0.0	+	.	consequence_type=missense_variant;id=rs150418753;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	625	625	0.0	+	.	consequence_type=synonymous_variant;id=rs757227703;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	626	626	0.0	+	.	consequence_type=missense_variant;id=rs781499966;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	631	631	0.0	+	.	consequence_type=missense_variant;id=rs746041079;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	632	632	0.0	+	.	consequence_type=missense_variant;id=rs756018179;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	634	634	0.0	+	.	consequence_type=synonymous_variant;id=rs369385342;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	636	636	0.0	+	.	consequence_type=missense_variant;id=rs779975972;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	652	652	0.0	+	.	consequence_type=synonymous_variant;id=rs768715452;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	662	662	0.0	+	.	consequence_type=missense_variant;id=rs774095582;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	664	664	0.0	+	.	consequence_type=synonymous_variant;id=rs199671891;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	670	670	0.0	+	.	consequence_type=synonymous_variant;id=rs112989351;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	671	671	0.0	+	.	consequence_type=missense_variant;id=rs1407256029;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	672	672	0.0	+	.	consequence_type=missense_variant;id=rs771441667;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	673	673	0.0	+	.	consequence_type=synonymous_variant;id=rs1330823537;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	676	676	0.0	+	.	consequence_type=synonymous_variant;id=rs1259991653;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	691	691	0.0	+	.	consequence_type=missense_variant;id=rs1303544092;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	692	692	0.0	+	.	consequence_type=missense_variant;id=rs919282095;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	694	694	0.0	+	.	consequence_type=synonymous_variant;id=rs772957252;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	700	700	0.0	+	.	consequence_type=missense_variant;id=rs375089291;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	703	703	0.0	+	.	consequence_type=synonymous_variant;id=rs770200317;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	714	714	0.0	+	.	consequence_type=missense_variant;id=rs775829411;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	720	720	0.0	+	.	consequence_type=missense_variant;id=rs763238851;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	721	721	0.0	+	.	consequence_type=synonymous_variant;id=rs1490869430;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	725	725	0.0	+	.	consequence_type=missense_variant;id=rs1342497115;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	726	726	0.0	+	.	consequence_type=missense_variant;id=rs764674925;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	727	727	0.0	+	.	consequence_type=splice_region_variant;id=rs752735481;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	735	735	0.0	+	.	consequence_type=missense_variant;id=rs758261924;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	737	737	0.0	+	.	consequence_type=missense_variant;id=rs777621617;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	751	751	0.0	+	.	consequence_type=synonymous_variant;id=rs1336872685;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	758	758	0.0	+	.	consequence_type=missense_variant;id=rs1331451303;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	773	773	0.0	+	.	consequence_type=synonymous_variant;id=rs1006739593;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	775	775	0.0	+	.	consequence_type=synonymous_variant;id=rs1264834130;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	777	777	0.0	+	.	consequence_type=missense_variant;id=rs746537411;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	781	781	0.0	+	.	consequence_type=synonymous_variant;id=rs770379933;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	787	787	0.0	+	.	consequence_type=synonymous_variant;id=rs780855060;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	793	793	0.0	+	.	consequence_type=synonymous_variant;id=rs1163522330;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	794	794	0.0	+	.	consequence_type=missense_variant;id=rs1429798567;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	811	811	0.0	+	.	consequence_type=synonymous_variant;id=rs146578323;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	817	817	0.0	+	.	consequence_type=synonymous_variant;id=rs970102977;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	832	832	0.0	+	.	consequence_type=synonymous_variant;id=rs201216212;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	833	833	0.0	+	.	consequence_type=missense_variant;id=rs1422769066;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	836	836	0.0	+	.	consequence_type=missense_variant;id=rs367724198;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	839	839	0.0	+	.	consequence_type=missense_variant;id=rs371122860;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	844	844	0.0	+	.	consequence_type=synonymous_variant;id=rs766086965;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	849	849	0.0	+	.	consequence_type=missense_variant;id=rs1196654054;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	851	851	0.0	+	.	consequence_type=missense_variant;id=rs772467109;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	860	860	0.0	+	.	consequence_type=missense_variant;id=rs1302511754;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	862	862	0.0	+	.	consequence_type=synonymous_variant;id=rs773804544;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	864	864	0.0	+	.	consequence_type=missense_variant;id=rs766531390;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	865	865	0.0	+	.	consequence_type=synonymous_variant;id=rs777042262;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	871	871	0.0	+	.	consequence_type=synonymous_variant;id=rs1266795902;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	872	872	0.0	+	.	consequence_type=missense_variant;id=rs759663986;alleles=C%2CA%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	874	874	0.0	+	.	consequence_type=synonymous_variant;id=rs765144876;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	877	877	0.0	+	.	consequence_type=synonymous_variant;id=rs1284923476;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	883	883	0.0	+	.	consequence_type=synonymous_variant;id=rs2239922;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	884	884	0.0	+	.	consequence_type=missense_variant;id=rs376218058;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	888	888	0.0	+	.	consequence_type=missense_variant;id=rs764042790;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	892	892	0.0	+	.	consequence_type=synonymous_variant;id=rs1486522613;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	909	909	0.0	+	.	consequence_type=missense_variant;id=rs1204184516;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	923	923	0.0	+	.	consequence_type=missense_variant;id=rs1441741328;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	929	929	0.0	+	.	consequence_type=synonymous_variant;id=rs2239923;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	931	931	0.0	+	.	consequence_type=synonymous_variant;id=rs985161494;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	934	934	0.0	+	.	consequence_type=synonymous_variant;id=rs1379717035;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	940	940	0.0	+	.	consequence_type=synonymous_variant;id=rs779600514;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	946	946	0.0	+	.	consequence_type=synonymous_variant;id=rs1166748067;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	955	955	0.0	+	.	consequence_type=synonymous_variant;id=rs1350394216;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	962	962	0.0	+	.	consequence_type=missense_variant;id=rs1326078809;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	966	966	0.0	+	.	consequence_type=missense_variant;id=rs1435733070;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	973	973	0.0	+	.	consequence_type=missense_variant;id=rs1244829195;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	979	979	0.0	+	.	consequence_type=synonymous_variant;id=rs772701064;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	980	980	0.0	+	.	consequence_type=missense_variant;id=rs760110087;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	982	982	0.0	+	.	consequence_type=synonymous_variant;id=rs1489341607;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	984	984	0.0	+	.	consequence_type=missense_variant;id=rs1291541781;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	988	988	0.0	+	.	consequence_type=synonymous_variant;id=rs1296557184;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	991	991	0.0	+	.	consequence_type=synonymous_variant;id=rs1378878097;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	995	995	0.0	+	.	consequence_type=missense_variant;id=rs1447003290;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	996	996	0.0	+	.	consequence_type=missense_variant;id=rs1384334634;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	997	997	0.0	+	.	consequence_type=synonymous_variant;id=rs748936607;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	999	999	0.0	+	.	consequence_type=missense_variant;id=rs1193969791;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1001	1001	0.0	+	.	consequence_type=missense_variant;id=rs1373930583;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1007	1007	0.0	+	.	consequence_type=missense_variant;id=rs767459640;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1008	1008	0.0	+	.	consequence_type=missense_variant;id=rs750330678;alleles=C%2CA%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1009	1009	0.0	+	.	consequence_type=splice_region_variant;id=rs913514091;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1010	1010	0.0	+	.	consequence_type=missense_variant;id=rs1271946369;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1016	1016	0.0	+	.	consequence_type=missense_variant;id=rs1213935690;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1017	1017	0.0	+	.	consequence_type=missense_variant;id=rs375623297;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1018	1018	0.0	+	.	consequence_type=synonymous_variant;id=rs1258804913;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1019	1019	0.0	+	.	consequence_type=missense_variant;id=rs760138330;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1020	1020	0.0	+	.	consequence_type=missense_variant;id=rs1336327252;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1027	1027	0.0	+	.	consequence_type=synonymous_variant;id=rs1397891517;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1028	1028	0.0	+	.	consequence_type=stop_gained;id=rs1415777939;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1034	1034	0.0	+	.	consequence_type=missense_variant;id=rs554809034;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1042	1042	0.0	+	.	consequence_type=synonymous_variant;id=rs1438572701;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1047	1047	0.0	+	.	consequence_type=missense_variant;id=rs3194194;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1052	1052	0.0	+	.	consequence_type=missense_variant;id=rs1358012081;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1054	1054	0.0	+	.	consequence_type=synonymous_variant;id=rs1445179731;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1055	1055	0.0	+	.	consequence_type=missense_variant;id=rs753488937;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1060	1060	0.0	+	.	consequence_type=synonymous_variant;id=rs1342923786;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1061	1061	0.0	+	.	consequence_type=missense_variant;id=rs754671896;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1067	1067	0.0	+	.	consequence_type=missense_variant;id=rs778639871;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1075	1075	0.0	+	.	consequence_type=synonymous_variant;id=rs751985902;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1077	1077	0.0	+	.	consequence_type=missense_variant;id=rs757647993;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1078	1078	0.0	+	.	consequence_type=synonymous_variant;id=rs781580851;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1084	1084	0.0	+	.	consequence_type=missense_variant;id=rs1442131409;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1094	1094	0.0	+	.	consequence_type=missense_variant;id=rs1396950068;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1101	1101	0.0	+	.	consequence_type=missense_variant;id=rs1208099201;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1102	1102	0.0	+	.	consequence_type=synonymous_variant;id=rs746356993;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1103	1103	0.0	+	.	consequence_type=missense_variant;id=rs1352058986;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1105	1105	0.0	+	.	consequence_type=synonymous_variant;id=rs769815313;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1106	1106	0.0	+	.	consequence_type=missense_variant;id=rs148483868;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1107	1107	0.0	+	.	consequence_type=missense_variant;id=rs1192890144;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1108	1108	0.0	+	.	consequence_type=synonymous_variant;id=rs924982378;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1123	1123	0.0	+	.	consequence_type=synonymous_variant;id=rs1364693881;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1127	1127	0.0	+	.	consequence_type=missense_variant;id=rs943116623;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1142	1142	0.0	+	.	consequence_type=missense_variant;id=rs1478893273;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1144	1144	0.0	+	.	consequence_type=synonymous_variant;id=rs749581366;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1147	1147	0.0	+	.	consequence_type=synonymous_variant;id=rs1424024037;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1154	1154	0.0	+	.	consequence_type=missense_variant;id=rs1412459058;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1159	1159	0.0	+	.	consequence_type=synonymous_variant;id=rs1038857011;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1160	1160	0.0	+	.	consequence_type=missense_variant;id=rs1360643122;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1166	1166	0.0	+	.	consequence_type=missense_variant;id=rs1401094663;alleles=T%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1168	1168	0.0	+	.	consequence_type=synonymous_variant;id=rs768875089;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1171	1171	0.0	+	.	consequence_type=synonymous_variant;id=rs901665795;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1172	1172	0.0	+	.	consequence_type=missense_variant;id=rs1324984572;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1174	1174	0.0	+	.	consequence_type=synonymous_variant;id=rs774502405;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1177	1177	0.0	+	.	consequence_type=missense_variant;id=rs1275875591;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1179	1179	0.0	+	.	consequence_type=missense_variant;id=rs1259100523;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1180	1180	0.0	+	.	consequence_type=splice_region_variant;id=rs142226258;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1181	1181	0.0	+	.	consequence_type=missense_variant;id=rs749387380;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1182	1182	0.0	+	.	consequence_type=missense_variant;id=rs1288820933;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1186	1186	0.0	+	.	consequence_type=synonymous_variant;id=rs369014766;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1187	1187	0.0	+	.	consequence_type=missense_variant;id=rs779143534;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1190	1190	0.0	+	.	consequence_type=missense_variant;id=rs748344051;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1191	1191	0.0	+	.	consequence_type=missense_variant;id=rs983756350;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1198	1198	0.0	+	.	consequence_type=synonymous_variant;id=rs771817702;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1218	1218	0.0	+	.	consequence_type=missense_variant;id=rs773052955;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1219	1219	0.0	+	.	consequence_type=synonymous_variant;id=rs746713731;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1232	1232	0.0	+	.	consequence_type=missense_variant;id=rs770912575;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1240	1240	0.0	+	.	consequence_type=synonymous_variant;id=rs1164368260;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1248	1248	0.0	+	.	consequence_type=missense_variant;id=rs776660504;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1249	1249	0.0	+	.	consequence_type=synonymous_variant;id=rs759148893;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1257	1257	0.0	+	.	consequence_type=missense_variant;id=rs1333869222;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1258	1258	0.0	+	.	consequence_type=missense_variant;id=rs1186266047;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1261	1261	0.0	+	.	consequence_type=synonymous_variant;id=rs773592883;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1276	1276	0.0	+	.	consequence_type=synonymous_variant;id=rs1180139152;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1282	1282	0.0	+	.	consequence_type=synonymous_variant;id=rs764809965;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1284	1284	0.0	+	.	consequence_type=missense_variant;id=rs775334053;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1285	1285	0.0	+	.	consequence_type=synonymous_variant;id=rs143838999;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1286	1286	0.0	+	.	consequence_type=missense_variant;id=rs767839828;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1297	1297	0.0	+	.	consequence_type=missense_variant;id=rs1462397852;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1318	1318	0.0	+	.	consequence_type=missense_variant;id=rs750807200;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1321	1321	0.0	+	.	consequence_type=synonymous_variant;id=rs766390878;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1322	1322	0.0	+	.	consequence_type=missense_variant;id=rs766935430;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1324	1324	0.0	+	.	consequence_type=synonymous_variant;id=rs754018187;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1325	1325	0.0	+	.	consequence_type=missense_variant;id=rs755095071;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1328	1328	0.0	+	.	consequence_type=missense_variant;id=rs1241960333;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1336	1336	0.0	+	.	consequence_type=synonymous_variant;id=rs1057442373;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1337	1337	0.0	+	.	consequence_type=missense_variant;id=rs867687573;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1339	1339	0.0	+	.	consequence_type=synonymous_variant;id=rs778948819;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1355	1355	0.0	+	.	consequence_type=missense_variant;id=rs1802201;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1363	1363	0.0	+	.	consequence_type=missense_variant;id=rs908761902;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1365	1365	0.0	+	.	consequence_type=missense_variant;id=rs1350193710;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1367	1367	0.0	+	.	consequence_type=missense_variant;id=rs1460724762;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1368	1368	0.0	+	.	consequence_type=missense_variant;id=rs1279886973;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1375	1375	0.0	+	.	consequence_type=synonymous_variant;id=rs771722999;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1379	1379	0.0	+	.	consequence_type=missense_variant;id=rs1276441766;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1388	1388	0.0	+	.	consequence_type=missense_variant;id=rs1401993695;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1392	1392	0.0	+	.	consequence_type=missense_variant;id=rs772801108;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1393	1393	0.0	+	.	consequence_type=synonymous_variant;id=rs376284001;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1396	1396	0.0	+	.	consequence_type=synonymous_variant;id=rs556448466;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1397	1397	0.0	+	.	consequence_type=missense_variant;id=rs141629884;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1399	1399	0.0	+	.	consequence_type=synonymous_variant;id=rs372878120;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1408	1408	0.0	+	.	consequence_type=synonymous_variant;id=rs763355938;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1417	1417	0.0	+	.	consequence_type=synonymous_variant;id=rs369290804;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1418	1418	0.0	+	.	consequence_type=missense_variant;id=rs774301899;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1420	1420	0.0	+	.	consequence_type=frameshift_variant;id=rs1459236506;alleles=A%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1426	1426	0.0	+	.	consequence_type=synonymous_variant;id=rs1199543349;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1427	1427	0.0	+	.	consequence_type=missense_variant;id=rs1232327561;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1449	1449	0.0	+	.	consequence_type=missense_variant;id=rs1426104773;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1453	1453	0.0	+	.	consequence_type=synonymous_variant;id=rs373214072;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1456	1456	0.0	+	.	consequence_type=missense_variant;id=rs867051835;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1458	1458	0.0	+	.	consequence_type=missense_variant;id=rs898816298;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1462	1462	0.0	+	.	consequence_type=synonymous_variant;id=rs767877724;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1465	1465	0.0	+	.	consequence_type=synonymous_variant;id=rs200139594;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1469	1469	0.0	+	.	consequence_type=missense_variant;id=rs1474867123;alleles=A%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1473	1473	0.0	+	.	consequence_type=missense_variant;id=rs1162489791;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1476	1476	0.0	+	.	consequence_type=missense_variant;id=rs1425544391;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1479	1479	0.0	+	.	consequence_type=missense_variant;id=rs578117787;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1480	1480	0.0	+	.	consequence_type=synonymous_variant;id=rs1327777743;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1481	1481	0.0	+	.	consequence_type=missense_variant;id=rs766069961;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1482	1482	0.0	+	.	consequence_type=missense_variant;id=rs1449583852;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1490	1490	0.0	+	.	consequence_type=missense_variant;id=rs765115917;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1495	1495	0.0	+	.	consequence_type=synonymous_variant;id=rs752598763;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1496	1496	0.0	+	.	consequence_type=synonymous_variant;id=rs1330209973;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1498	1498	0.0	+	.	consequence_type=synonymous_variant;id=rs1465973808;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1503	1503	0.0	+	.	consequence_type=stop_lost;id=rs1421300928;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1506	1506	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1288068012;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1510	1510	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs747853709;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1512	1512	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1192178645;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1514	1515	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs763336808;alleles=-%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1516	1516	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1191436418;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1518	1518	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1393899624;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1519	1519	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs370761943;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1522	1522	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs756865994;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1525	1525	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1053733;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1528	1528	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1462863066;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1534	1534	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1401838250;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1541	1541	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749639976;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1545	1545	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs769028747;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1546	1546	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs371753337;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1561	1562	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1275487350;alleles=-%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1570	1570	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs369051195;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1573	1573	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1250182993;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1574	1574	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs374157641;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1580	1580	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs565164528;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1581	1581	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1037729069;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1592	1592	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141202848;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1593	1593	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541333000;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1595	1595	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs559236400;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1600	1600	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs981524641;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1605	1605	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1053739;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1606	1606	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1321337667;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1614	1614	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1171204481;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1619	1619	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1391338066;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1626	1626	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1165345478;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1628	1628	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs934409916;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1629	1629	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1054232876;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1631	1631	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178276522;alleles=T%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1635	1635	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1470631130;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1641	1641	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs960277341;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1642	1642	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs914389525;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1644	1644	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs771408813;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1647	1647	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs547873231;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1648	1648	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs563091154;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1654	1654	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs530405653;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1656	1656	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs551792359;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1667	1667	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs979139564;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1668	1668	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs891044536;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1670	1670	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1008191100;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1673	1673	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs114271764;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1674	1674	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1334496147;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1682	1682	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs964751422;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1683	1683	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897217919;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1687	1687	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs143311253;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1696	1696	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs923189525;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1697	1697	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs148324496;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1698	1698	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1401550841;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1700	1700	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs548069555;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1701	1701	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs566098238;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1705	1705	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1189649614;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1715	1715	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs959532407;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1716	1716	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1251272836;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1737	1737	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1462186783;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1738	1738	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1012864617;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1741	1741	0.0	+	.	consequence_type=splice_region_variant;id=rs1269977841;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1744	1744	0.0	+	.	consequence_type=splice_donor_variant;id=rs1202296343;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1745	1745	0.0	+	.	consequence_type=splice_region_variant;id=rs933216623;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1748	1748	0.0	+	.	consequence_type=splice_region_variant;id=rs1025193535;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1749	1749	0.0	+	.	consequence_type=splice_region_variant;id=rs971403946;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1761	1761	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs981101330;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1784	1784	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs369699233;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1791	1791	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1218212438;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1798	1798	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs942121531;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1808	1808	0.0	+	.	consequence_type=splice_region_variant;id=rs1187332688;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1811	1811	0.0	+	.	consequence_type=splice_donor_variant;id=rs1421671608;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1823	1825	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1398111547;alleles=AGT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1825	1826	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1037801267;alleles=TA%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1828	1828	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1414106419;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1830	1830	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1430514004;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1831	1831	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs989895551;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1833	1837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1001942416;alleles=TATAT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1837	1838	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1010428709;alleles=-%2CTA
CDS|ENST00000258960	dbSNP	sequence_variant	1841	1841	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1209063133;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1847	1847	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs932467552;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1853	1853	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224841958;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1856	1857	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1429876784;alleles=-%2CTAAATA
CDS|ENST00000258960	dbSNP	sequence_variant	1863	1866	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1264823314;alleles=TCTT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1880	1880	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1317026015;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1894	1894	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1020440494;alleles=G%2CC%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1900	1900	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs17684744;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1917	1917	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs16939858;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1918	1919	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1407087325;alleles=AG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1934	1934	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1338891400;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1942	1942	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs796506744;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1943	1943	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs769885556;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1949	1949	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1423280480;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1955	1955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1036938272;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1956	1956	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1171753731;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1960	1960	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1032510694;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1962	1962	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897144744;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1963	1963	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1359202111;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1964	1964	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs995508376;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1965	1965	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1048457718;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1966	1966	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244625323;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1972	1972	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs576637742;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1982	1982	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1196289397;alleles=T%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1988	1988	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs537427196;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1996	1996	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs895230067;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1998	1998	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs558645892;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2003	2003	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1012378907;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2009	2009	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1225957412;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2020	2021	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1261580556;alleles=AG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2025	2025	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs970947658;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2029	2029	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs577172913;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2035	2035	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1231594463;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2055	2055	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs757917677;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2066	2066	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1319821569;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2076	2076	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs775653407;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2083	2083	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1216711171;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2084	2084	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1031296585;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2090	2090	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955683670;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2098	2098	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1444766255;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2106	2106	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1400102884;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2108	2108	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1299100514;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2120	2120	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs973220799;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2123	2123	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs989821734;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2125	2125	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1348665604;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2129	2129	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs540927831;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2139	2166	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244092003;alleles=CTGGGGCTGACCCTGGGCAGGGACTTTC%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2167	2167	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs953948699;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2174	2174	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs559716890;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2176	2176	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438688265;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2180	2180	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1251023194;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2187	2187	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178702703;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2189	2189	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs574557884;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2191	2191	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs943909863;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2192	2192	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs972624417;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2205	2205	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs918540028;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2210	2210	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs376815066;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2211	2211	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1161070547;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2212	2212	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1238339324;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2219	2219	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1335370299;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2228	2228	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs724329;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2231	2234	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1343049988;alleles=ATTG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2242	2242	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1452671782;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2248	2248	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1365847420;alleles=T%2CA%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2259	2259	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141446378;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2262	2262	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1366968827;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2266	2266	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1000329032;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2271	2271	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs530491484;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2276	2276	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1364043446;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2279	2279	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs895200885;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2281	2281	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1160791533;alleles=C%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2282	2282	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs900289262;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2284	2284	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1407230545;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2295	2295	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200135795;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2298	2298	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1490819689;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2302	2302	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178689600;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2320	2320	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs995920796;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2324	2324	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1367298964;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2327	2327	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs948121222;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2328	2328	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1349991909;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2329	2329	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1430002785;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2333	2333	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1241377536;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2341	2341	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs766348222;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2344	2344	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283035619;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2349	2349	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906689685;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2351	2351	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs180906761;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2356	2356	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1381193691;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2357	2357	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs954372227;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2359	2359	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1290282779;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2382	2382	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs28421762;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2383	2383	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1376926156;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2387	2387	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs894064577;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2399	2399	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1176852360;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2409	2409	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1011223354;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2411	2411	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1292507701;alleles=G%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2416	2416	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1192761554;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2428	2428	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs963254927;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2440	2440	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446511726;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2442	2442	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs528096327;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2443	2443	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1207185525;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2447	2447	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1482380396;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2450	2450	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs927144783;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2460	2460	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs761146565;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2462	2462	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs374822197;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2467	2467	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1326049059;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2476	2476	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1276862106;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2479	2479	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs770774164;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2483	2483	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs992941793;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2498	2498	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1326564744;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2504	2504	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1319714625;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2517	2517	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs985595681;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2522	2522	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1393970382;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2529	2529	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1404878473;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2537	2537	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955974070;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2539	2539	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1019400127;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2540	2540	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs780821197;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2544	2544	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs187009810;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2545	2545	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541212507;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2549	2549	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1041667828;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2552	2552	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1167318932;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2553	2553	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1475696264;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2554	2554	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1405598391;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2556	2556	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs918466416;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2557	2557	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1195385529;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2563	2563	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs931250499;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2569	2569	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1418077431;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2576	2576	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1204475602;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2583	2583	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1256548861;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2593	2593	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1195796732;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2600	2600	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1340643287;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2610	2610	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1271484221;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2611	2611	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs753837145;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2627	2627	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs984029791;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2632	2632	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1242015093;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2635	2635	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs916548110;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2640	2640	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs904818644;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2641	2641	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1315323350;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2646	2646	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1366838555;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2648	2648	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1465089486;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2649	2649	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs16939861;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2656	2656	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1327902327;alleles=A%2CC%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2658	2658	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541902389;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2661	2661	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1349791305;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2665	2665	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1040300793;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2685	2685	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs192258080;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2686	2686	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1184502065;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2687	2687	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446668586;alleles=T%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2705	2705	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1281634906;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2706	2706	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1371638005;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2711	2711	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438706527;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2718	2718	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs998731903;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2720	2720	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1275764200;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2724	2725	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1030099529;alleles=-%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2730	2730	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs754485882;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2737	2737	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs369197832;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2742	2742	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906625325;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2754	2754	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs935447272;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2762	2762	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1316025087;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2764	2765	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1168224551;alleles=-%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2767	2767	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1052622495;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2769	2769	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs548833697;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2779	2779	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs894035026;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2782	2782	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1014589512;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2793	2793	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438321414;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2794	2794	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1442698911;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2796	2796	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1011149983;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2798	2798	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs370020780;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2799	2799	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1206537935;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2801	2801	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1404245218;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2804	2804	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1230903280;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2806	2806	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs138084835;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2814	2814	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1034654056;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2818	2818	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1406095157;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2819	2819	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs958585513;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2833	2833	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs537513780;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2835	2837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs771687715;alleles=CCG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2845	2845	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269034032;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2852	2852	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224099346;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2863	2863	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1350810764;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2867	2867	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283125289;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2869	2869	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs35368650;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2870	2870	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1272855697;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2871	2871	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs374358296;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2874	2874	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs925938357;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2894	2894	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs535065893;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2896	2896	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1346048996;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2898	2902	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1410955251;alleles=AAGCA%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	2919	2919	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs993940078;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2920	2920	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1406881834;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2923	2923	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1343445367;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2927	2927	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs936279227;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2928	2928	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1039969234;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2931	2931	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1410667852;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2938	2938	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs552972231;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2939	2939	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446464723;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2941	2941	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1337855592;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2945	2945	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs952568428;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2950	2950	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1484614726;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2951	2951	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs752361277;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2952	2952	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244138051;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2954	2954	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs934177673;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2955	2955	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1448342009;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2959	2959	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283604944;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2965	2965	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs916534207;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2966	2966	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1216205215;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2967	2967	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs890242585;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2969	2969	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs758034998;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2970	2970	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1204035918;alleles=A%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2971	2971	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs553041259;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	2979	2979	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1216704574;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	2980	2980	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs982135924;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2996	2996	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1459697651;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3003	3003	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269636882;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3022	3022	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs898846971;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3023	3023	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541738745;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3024	3024	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs935414689;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3028	3028	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1407225788;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3035	3035	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs12449780;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3040	3041	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1356099906;alleles=-%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3043	3043	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs11548428;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3046	3046	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1427254414;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3049	3049	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1034274080;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3050	3060	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1186574299;alleles=GGCTTGTTGCA%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3065	3065	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs946908519;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3077	3077	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1461617225;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3079	3079	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs556712929;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3086	3086	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1417962663;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3089	3089	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1202398712;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3098	3098	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs889384859;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3099	3099	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1215270939;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3102	3103	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1364084510;alleles=AG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3112	3112	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1406322662;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3124	3124	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs143759450;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3126	3126	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs977463771;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3127	3127	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1339071335;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3135	3135	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs183449664;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3138	3138	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs900904651;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3141	3141	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs757632957;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3144	3144	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1333781433;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3146	3146	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1411163563;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3147	3147	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1382794105;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3152	3152	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1025384349;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3155	3155	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs781629571;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3156	3156	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1444829035;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3165	3165	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1244793198;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3168	3168	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1005390105;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3170	3170	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs975779870;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3171	3171	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1023933916;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3177	3177	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs934227498;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3178	3178	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1051303465;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3183	3183	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs908689377;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3186	3186	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1245603780;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3193	3193	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs564244625;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3194	3194	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1360420160;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3195	3195	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1315035585;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3199	3199	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1390032565;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3203	3204	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs35225641;alleles=-%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3227	3227	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs746408568;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3232	3232	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224119541;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3233	3233	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1299260497;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3248	3248	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs775429324;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3249	3249	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1363250321;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3253	3254	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1264705091;alleles=-%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3257	3257	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1316745110;alleles=C%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3258	3258	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386715308;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3259	3259	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1321174504;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3260	3260	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs769836303;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3261	3261	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1262034984;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3262	3262	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1178920999;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3279	3279	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1448418611;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3287	3287	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs775600347;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3288	3288	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs940143966;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3289	3306	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1490514482;alleles=TGACTGACGTTTGCTCCT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3312	3312	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308112860;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3313	3313	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs982492718;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3324	3324	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1431840999;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3329	3329	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs927938344;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3331	3331	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs528068964;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3332	3332	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs956715924;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3340	3340	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs988222284;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3355	3355	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749516447;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3356	3356	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1172397901;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3358	3358	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1385919379;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3378	3378	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs946835113;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3383	3383	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1050620364;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3384	3384	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs910773287;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3386	3386	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs944993602;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3410	3410	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs894433375;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3418	3418	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs540250520;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3421	3421	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1161001321;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3422	3422	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1041047055;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3427	3427	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs774477716;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3430	3430	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs993827034;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3432	3432	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200007511;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3435	3435	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1480815947;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3442	3442	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269527506;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3445	3445	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1203649309;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3452	3452	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1405424311;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3460	3460	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1485660044;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3465	3465	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1285144548;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3466	3466	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs879076610;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3467	3467	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs768824847;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3475	3475	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1046763137;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3476	3476	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1210979641;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3491	3491	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs888199407;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3498	3498	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs560072132;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3500	3500	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs530382672;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3508	3508	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283231811;alleles=A%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3520	3520	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs2269746;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3521	3521	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1332360553;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3522	3522	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1352385209;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3525	3525	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1292818858;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3527	3527	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1033099011;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3541	3542	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1385237938;alleles=-%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3548	3548	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1322059129;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3562	3562	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs957649196;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3564	3564	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1405017960;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3566	3566	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs975471918;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3567	3567	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1481357305;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3568	3568	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1379508682;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3570	3570	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1309733064;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3571	3571	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1028738032;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3588	3588	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1427930374;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3602	3602	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs570223309;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3607	3607	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1023481224;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3608	3608	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs905053344;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3615	3615	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1003444775;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3616	3616	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1490376937;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3624	3625	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1223826001;alleles=CT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3632	3632	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955670344;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3633	3633	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs531175480;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3642	3642	0.0	+	.	consequence_type=splice_acceptor_variant;id=rs908772709;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3643	3643	0.0	+	.	consequence_type=splice_acceptor_variant;id=rs760326328;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3647	3647	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs766296948;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3658	3658	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs974205497;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3659	3659	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs147214037;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3660	3660	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1381816278;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3666	3666	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1415905438;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3668	3668	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1394259462;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3677	3678	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141401145;alleles=-%2CGGG
CDS|ENST00000258960	dbSNP	sequence_variant	3682	3682	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1157100100;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3696	3698	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1461567461;alleles=CTC%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3703	3703	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs968180288;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3708	3708	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1443007106;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3710	3710	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs140336433;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3711	3711	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1359930443;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3713	3713	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs930386786;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3718	3718	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs986678164;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3732	3732	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1249073442;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3738	3738	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs910710077;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3739	3739	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1989802;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3741	3741	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs553298659;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3742	3742	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs142694577;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3743	3743	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386203552;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3744	3744	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs761868545;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3747	3747	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1337321748;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3749	3749	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs574325904;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3753	3753	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1328158733;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3756	3756	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1391867226;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3762	3762	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1371318412;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3768	3768	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs764818146;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3769	3769	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs919516938;alleles=G%2CA%2CC%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3787	3787	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs929604101;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3795	3795	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs187295973;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3796	3796	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs888166470;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3797	3797	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs3214106;alleles=T%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3799	3799	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs397839901;alleles=T%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	3805	3805	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1224040282;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3808	3808	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1289033696;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3817	3817	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1253414817;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3818	3818	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs997320577;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3822	3822	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs144416810;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3837	3837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1292084177;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3840	3840	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955369588;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3844	3844	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1348327259;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3848	3848	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs751249150;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3849	3849	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1045241182;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3850	3850	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs755604520;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3861	3861	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs905022668;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3864	3864	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1352271352;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3865	3865	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs77946949;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3866	3866	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1403213945;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3867	3867	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1439947020;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3874	3874	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs547051568;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3875	3875	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1379886654;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3886	3886	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs892391956;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3887	3887	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs961616835;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3894	3895	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1383339545;alleles=-%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3896	3896	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1158337296;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3899	3899	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs774283266;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3900	3900	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs190636525;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3902	3902	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1457290710;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3904	3904	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1479853735;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3906	3906	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1246754349;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3909	3909	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs565687243;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3910	3910	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs182422410;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3915	3915	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1283050785;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3924	3924	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs188355789;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3925	3925	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1444269533;alleles=C%2CA%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	3933	3933	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1281320353;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3934	3934	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs539966111;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3940	3940	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs200266826;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3941	3941	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs148432087;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3942	3942	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs542532260;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3944	3944	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1324919529;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3949	3949	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs919485924;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3951	3951	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1312197328;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3957	3957	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1320607191;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3963	3963	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs142546587;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3964	3964	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs150884493;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3968	3968	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs552771831;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3983	3983	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1425334483;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3987	3987	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1192441986;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3989	3989	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1989803;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3991	3991	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs996662517;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3996	3996	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1044812746;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3997	3997	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1989804;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4000	4000	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs939160862;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4002	4002	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1312685053;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4003	4003	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1185666305;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4014	4014	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1221017211;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4026	4026	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1359901535;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4028	4029	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs34744705;alleles=-%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4032	4032	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269886501;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4035	4035	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1254108565;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4038	4038	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1367882615;alleles=C%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4038	4038	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1423351568;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4040	4040	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1335128053;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4042	4042	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1056331855;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4043	4043	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1028830330;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4044	4044	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs139674606;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4054	4054	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1009476590;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4056	4056	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs192155766;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4057	4057	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1418135469;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4058	4058	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs903842957;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4061	4061	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1169691551;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4064	4064	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs961646708;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4068	4068	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1454196689;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4073	4073	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1182764305;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4074	4075	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1377763196;alleles=-%2CCCTCCCAG
CDS|ENST00000258960	dbSNP	sequence_variant	4076	4076	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs780182043;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4077	4079	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1382272062;alleles=TTC%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4082	4083	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1297164419;alleles=-%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4085	4085	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs745510279;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4086	4086	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1202335769;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4096	4096	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs531998526;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4102	4102	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs550454414;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4107	4107	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1229489407;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4120	4120	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs959825452;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4122	4122	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs997609682;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4128	4128	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs569160208;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4129	4129	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs539239556;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4135	4135	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs547487392;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4136	4136	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1305161174;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4137	4137	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1026426534;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4139	4139	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1353484693;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4141	4141	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs557899355;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4147	4147	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308094768;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4148	4148	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs569814923;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4154	4154	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs144545088;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4157	4157	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1431040974;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4164	4164	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1383004525;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4166	4166	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs533836199;alleles=A%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4168	4168	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1424233255;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4169	4169	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1254450780;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4172	4172	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1415662028;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4178	4178	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs12936003;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4179	4179	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs541600919;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4183	4183	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs962373075;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4184	4184	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs544254488;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4189	4189	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs563957742;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4191	4191	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs980849596;alleles=G%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4199	4199	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749256414;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4201	4201	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1322740022;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4202	4202	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs575861858;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4204	4204	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs926371390;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4205	4205	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1350420604;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4209	4209	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1470853672;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4220	4220	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1173749197;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4231	4231	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1358196928;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4236	4236	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs939097785;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4237	4238	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1454048669;alleles=TG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4240	4240	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1008298671;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4245	4245	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs778951530;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4257	4257	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs193078436;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4260	4260	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1337790259;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4270	4270	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897173445;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4276	4276	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs995497441;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4279	4279	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1027651561;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4286	4292	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs959615103;alleles=ATGGAAA%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4294	4294	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1278151802;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4302	4302	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1346739321;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4305	4305	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1488921375;alleles=C%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4306	4306	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1221273215;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4307	4307	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs945223332;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4316	4319	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1299713857;alleles=CTGT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4322	4322	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1214091270;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4331	4331	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1025095889;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4332	4332	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs903769489;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4337	4337	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs981141232;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4342	4342	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386792118;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4345	4345	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs924334554;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4346	4346	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1007533963;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4354	4354	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1286717016;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4361	4361	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1452821185;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4362	4362	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs770817008;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4363	4363	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs901871985;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4366	4366	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs878981029;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4367	4367	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs989799803;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4369	4369	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1427357837;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4371	4371	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs914510020;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4373	4373	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1215757676;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4387	4387	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs868032669;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4391	4391	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1269479940;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4392	4392	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs78867706;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4393	4393	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs546676595;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4395	4395	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs749218149;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4396	4396	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1211190168;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4397	4397	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs868806036;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4398	4398	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs943825011;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4399	4399	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1026396864;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4400	4400	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1037137398;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4412	4415	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs897205397;alleles=AACC%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4428	4428	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1433862222;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4433	4433	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1365743509;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4443	4443	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1322283760;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4448	4448	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1450115395;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4449	4449	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs950877614;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4456	4456	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1173045404;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4465	4465	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1048382196;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4466	4468	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1379420648;alleles=AGA%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4470	4470	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1358022791;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4471	4471	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1449080582;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4477	4477	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs561891221;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4482	4482	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs368287374;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4484	4484	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1006353220;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4492	4492	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs577035381;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4493	4493	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1460229676;alleles=A%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4497	4497	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1418523760;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4503	4503	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1201507011;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4507	4507	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1483970890;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4509	4509	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1303283049;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4511	4511	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1366718155;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4519	4519	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs184426663;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4520	4520	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs550593694;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4529	4529	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs146633312;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4542	4542	0.0	+	.	consequence_type=splice_acceptor_variant;id=rs1339596894;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4543	4543	0.0	+	.	consequence_type=splice_region_variant;id=rs926270475;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4548	4548	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1339338471;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4551	4551	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs12723;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4564	4564	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs762322394;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4573	4573	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs999623239;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4576	4576	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs960386125;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4580	4580	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs991907782;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4583	4583	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1351838802;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4592	4592	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1404515789;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4594	4594	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs913659066;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4603	4603	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1306279725;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4609	4609	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs116783088;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4611	4611	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1391053186;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4612	4612	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955809507;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4615	4615	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs75772115;alleles=C%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4626	4626	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs768617425;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4627	4627	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1021274457;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4634	4634	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs943266937;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4639	4639	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs566620609;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4640	4640	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs534025851;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4651	4651	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs187764117;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4652	4652	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs376074145;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4654	4654	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1355425511;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4658	4660	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1438757711;alleles=TGT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4667	4667	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs972526380;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4668	4668	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1047770564;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4685	4685	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1287608514;alleles=T%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4695	4695	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs11548430;alleles=C%2CA%2CG%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4702	4702	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386562475;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4717	4717	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1403810719;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4718	4718	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1390535430;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4720	4720	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1006323540;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4725	4725	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1164212346;alleles=G%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4726	4726	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1473940853;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4730	4730	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs537955893;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4736	4736	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs556169662;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4737	4737	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906062210;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4739	4739	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1349622073;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4744	4744	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1472659160;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4747	4747	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1253304992;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4749	4749	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1002177925;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4774	4774	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs878909110;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4778	4779	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs906753161;alleles=-%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4780	4780	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs546438804;alleles=G%2CA%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4783	4783	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1446413412;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4790	4790	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1290273986;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4792	4792	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1434321670;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4796	4796	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs991824327;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4799	4799	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1330745525;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4802	4802	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs372498096;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4803	4803	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1011314340;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4813	4813	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1386877848;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4822	4822	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1315742111;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4829	4829	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs767858850;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4833	4833	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1458224860;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4842	4842	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1358585731;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4844	4844	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs141266275;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4845	4845	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1170305096;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4847	4847	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1477387533;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4848	4848	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1289016599;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4853	4853	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200521307;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4861	4864	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308053456;alleles=AAAG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	4872	4872	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1200289824;alleles=C%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4873	4873	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs112206165;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4878	4878	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1236208595;alleles=A%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	48	48	0.0	+	.	consequence_type=missense_variant;id=rs756082410;alleles=C%2CA%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	49	49	0.0	+	.	consequence_type=synonymous_variant;id=rs780444510;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	50	50	0.0	+	.	consequence_type=missense_variant;id=rs1424340537;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	51	51	0.0	+	.	consequence_type=missense_variant;id=rs973343235;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	53	53	0.0	+	.	consequence_type=missense_variant;id=rs754859910;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	54	54	0.0	+	.	consequence_type=missense_variant;id=rs1356403688;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	57	57	0.0	+	.	consequence_type=missense_variant;id=rs202061902;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	59	59	0.0	+	.	consequence_type=synonymous_variant;id=rs748150811;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	60	60	0.0	+	.	consequence_type=missense_variant;id=rs772038652;alleles=T%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	61	61	0.0	+	.	consequence_type=synonymous_variant;id=rs927228181;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	135	137	0.0	+	.	consequence_type=inframe_deletion;id=rs766213031;alleles=ACA%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	138	138	0.0	+	.	consequence_type=missense_variant;id=rs946116469;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	139	139	0.0	+	.	consequence_type=synonymous_variant;id=rs766535198;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	934	938	0.0	+	.	consequence_type=frameshift_variant;id=rs1056950860;alleles=TGAAG%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1515	1515	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs377286541;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1595	1596	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1308084346;alleles=GA%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1824	1825	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs199746970;alleles=-%2CTA
CDS|ENST00000258960	dbSNP	sequence_variant	1825	1825	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs955712879;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	1825	1837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs905921677;alleles=TATATATATATAT%2C-
CDS|ENST00000258960	dbSNP	sequence_variant	1826	1826	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1174239154;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	1836	1837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1477157222;alleles=-%2CTT
CDS|ENST00000258960	dbSNP	sequence_variant	1836	1836	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1057096455;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	1837	1837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs914358436;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1838	1838	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1169610627;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	1866	1866	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1470944382;alleles=T%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2021	2021	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1025575332;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2157	2157	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1164637646;alleles=A%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2158	2158	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1485040927;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2159	2159	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs117105863;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2162	2163	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs571677514;alleles=-%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2234	2234	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1041971745;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	2836	2836	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs559020504;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	2837	2837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs917340541;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3041	3041	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1052550601;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3052	3052	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1476082108;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3056	3056	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs915393689;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3254	3254	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1162366452;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3290	3290	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1267486371;alleles=G%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3292	3292	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1261918292;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3296	3296	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1477740070;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3297	3297	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs762891713;alleles=G%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	3698	3698	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1390845084;alleles=C%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	3739	3740	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1276112396;alleles=-%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	3896	3897	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1445524322;alleles=-%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4073	4074	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1300740579;alleles=-%2CCCCAG
CDS|ENST00000258960	dbSNP	sequence_variant	4270	4271	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1156685668;alleles=-%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4292	4292	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs913721217;alleles=A%2CG
CDS|ENST00000258960	dbSNP	sequence_variant	4317	4317	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs2239925;alleles=T%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4332	4333	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs770118889;alleles=-%2CC
CDS|ENST00000258960	dbSNP	sequence_variant	4415	4415	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1293059007;alleles=C%2CA
CDS|ENST00000258960	dbSNP	sequence_variant	4467	4467	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1160866224;alleles=G%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4779	4779	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs192440480;alleles=G%2CA%2CC%2CT
CDS|ENST00000258960	dbSNP	sequence_variant	4779	4779	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1290068700;alleles=G%2C-
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1506	1506	0.0	.	.	AC_Male=1;AF_NFE=8.97215e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-62;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08210e-06;Hom=0;AF_POPMAX=8.97215e-06;AN_POPMAX=111456;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.44524e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=55;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.12258e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=12/12,cDNA_position=1511,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000258960.2:c.*2C>G
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1510	1510	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=2.51189e-44;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08614e-06;Hom=0;AF_POPMAX=4.48672e-05;AN_POPMAX=22288;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.45123e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.48837e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.14055e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=T:0,cDNA_position=1515,ExAC_NFE_MAF=T:0.0001512,SYMBOL=NMT1,Existing_variation=rs747853709,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.*6C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1512	1512	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=6.30957e-54;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08707e-06;Hom=0;AF_POPMAX=4.48672e-05;AN_POPMAX=22288;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.45334e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.18605e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92644e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=12/12,cDNA_position=1517,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000258960.2:c.*8C>G
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1514	1514	0.0	.	.	AC_Male=4;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|2|1|1|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-26;AF_OTH=0.00000e+00;alleles=A%2CAG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.87102e-05;Hom=0;AF_POPMAX=2.96525e-04;AN_POPMAX=16862;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|1|2|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=2.99039e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=3.70370e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=2.72593e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|6;Hom_raw=0;AF_SAS=6.61638e-05;AS_RF=6.87752e-01;Hom_AMR=0;AC_EAS=5;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.96525e-04;AC_SAS=2;POPMAX=EAS;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84239e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:1.648e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,HGVS_OFFSET=1,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.0001156,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=G:0,cDNA_position=1519-1520,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763336808,VARIANT_CLASS=insertion,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000258960.2:c.*11dupG,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1515	1515	0.0	.	.	AC_Male=3;AF_NFE=2.69469e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15678e-88;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63716e-05;Hom=0;AF_POPMAX=3.29576e-05;AN_POPMAX=30342;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0;AF_Male=2.23857e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=9.06520e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=3.29576e-05;AS_RF=9.30036e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62425e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:2.472e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:4.496e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=A:0,cDNA_position=1520,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs377286541,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:2.471e-05,HGVSc=ENST00000258960.2:c.*11G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1516	1516	0.0	.	.	AC_Male=1;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-91;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09195e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.46035e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.16667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=60;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.46101e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=12/12,cDNA_position=1521,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000258960.2:c.*12T>A
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1518	1518	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.84034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10071e-06;Hom=0;AF_POPMAX=3.04099e-05;AN_POPMAX=32884;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.47507e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.77311e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.43019e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=3.04099e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=12/12,cDNA_position=1523,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000258960.2:c.*14C>T
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1519	1519	0.0	.	.	AC_Male=2;AF_NFE=2.70100e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|0|0|0|0|0|3|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=2.50594e-46;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=4.49115e-05;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.05460e-05;Hom=0;AF_POPMAX=6.57981e-05;AN_POPMAX=15198;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|2|0|0|0|0|2|0|1|0|0|0|1|0|0|0|0|0;AF_Male=1.49788e-05;AF_AFR=6.57981e-05;AC_raw=6;AB_MEDIAN=4.35216e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=2.73139e-05;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.16709e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:4.12e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.998e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0002,Allele=A,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=A:9.614e-05,cDNA_position=1524,ExAC_NFE_MAF=A:0.0001512,SYMBOL=NMT1,Existing_variation=rs370761943,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:4.118e-05,HGVSc=ENST00000258960.2:c.*15G>A,ExAC_Adj_MAF=A:8.643e-05
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1522	1522	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-68;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10624e-06;Hom=0;AF_POPMAX=6.57376e-05;AN_POPMAX=15212;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48413e-06;AF_AFR=6.57376e-05;AC_raw=1;AB_MEDIAN=5.38462e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.02328e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.239e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=C:9.615e-05,cDNA_position=1527,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs756865994,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.*18T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1525	1525	0.0	.	.	AC_Male=61593;AF_NFE=4.22062e-01;Hom_FIN=2448;GQ_MEDIAN=99;AB_HIST_ALT=0|2|56|292|736|1976|4000|7432|12641|12024|11096|4916|2284|797|303|124|43|27|28|0;AC_FIN=10454;DREF_MEDIAN=3.98107e-70;AF_OTH=4.62645e-01;alleles=G%2CA;AF_FIN=4.70689e-01;AC_OTH=2477;Hom_Male=14819;AC=112061;Hom_NFE=9865;AF=4.62481e-01;Hom=27067;AF_POPMAX=7.72167e-01;AN_POPMAX=16714;AC_NFE=46724;AS_FilterStatus=PASS;Hom_OTH=591;DP_HIST_ALT=26|1062|5268|9353|8716|6312|4899|4852|5720|6174|6017|5529|4737|3912|2917|2209|1744|1260|974|952;AF_Male=4.63210e-01;AF_AFR=3.48249e-01;AC_raw=114295;AB_MEDIAN=4.57627e-01;Hom_EAS=4996;AC_AMR=15494;AF_ASJ=4.67235e-01;DP_MEDIAN=42;AF_Female=4.61595e-01;GQ_HIST_ALT=23|40|51|158|301|286|785|1226|826|1543|1574|913|1410|1167|657|1035|863|585|831|72262;Hom_raw=27759;AF_SAS=4.72870e-01;AS_RF=9.54732e-01;Hom_AMR=3731;AC_EAS=12906;AC_Female=50468;Hom_AFR=919;Hom_ASJ=1055;AF_EAS=7.72167e-01;AC_SAS=14188;POPMAX=EAS;AC_POPMAX=12906;AC_AFR=5269;Hom_SAS=3462;AC_ASJ=4549;AF_raw=4.64104e-01;Hom_Female=12248;AF_AMR=4.77444e-01;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:0.4574,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0.4308,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0.3321,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.4239,AFR_MAF=A:0.4771,SWISSPROT=P30419,EAS_MAF=A:0.4755,EUR_MAF=A:0.7946,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.7698,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,GMAF=G:0.4940,STRAND=1,ExAC_SAS_MAF=A:0.4713,CCDS=CCDS11494.1,EA_MAF=A:0.3423,Allele=A,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=A:0.3473,cDNA_position=1530,ExAC_NFE_MAF=A:0.4712,SYMBOL=NMT1,Existing_variation=rs1053733,SAS_MAF=A:0.4712,VARIANT_CLASS=SNV,AA_MAF=A:0.501,MINIMISED=1,ExAC_AFR_MAF=A:0.457,HGVSc=ENST00000258960.2:c.*21G>A,ExAC_Adj_MAF=A:0.4795
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1534	1534	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.14817e-06;Hom=0;AF_POPMAX=3.14327e-05;AN_POPMAX=31814;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.81481e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.19709e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20180e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=3.14327e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,UNIPARC=UPI0000130275,Consequence=3_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=12/12,cDNA_position=1539,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000258960.2:c.*30C>T
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1541	1541	0.0	.	.	AC_Male=1;AF_NFE=2.71474e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-30;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.24726e-05;Hom=0;AF_POPMAX=2.71474e-05;AN_POPMAX=110508;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.57083e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.84430e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.36557e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.246e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=T:0,cDNA_position=1546,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749639976,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000258960.2:c.*37A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1545	1545	0.0	.	.	AC_Male=2;AF_NFE=2.71493e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|2|0|1|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-63;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.66312e-05;Hom=0;AF_POPMAX=6.60328e-05;AN_POPMAX=15144;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|1|0;AF_Male=1.51435e-05;AF_AFR=6.60328e-05;AC_raw=5;AB_MEDIAN=3.26087e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=1.84430e-05;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.31532e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03029e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:3.3e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.501e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=T:9.639e-05,cDNA_position=1550,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs769028747,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000258960.2:c.*41C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	3_prime_UTR_variant	1546	1546	0.0	.	.	AC_Male=6;AF_NFE=9.01599e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|1|1|1|0|3|2|4|4|2|2|3|1|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-31;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=22;Hom_NFE=0;AF=9.08033e-05;Hom=0;AF_POPMAX=1.23508e-03;AN_POPMAX=9716;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|6|2|5|2|1|2|1|0|1|1|1|0|1|1|0|0|0|0;AF_Male=4.51155e-05;AF_AFR=5.28053e-04;AC_raw=25;AB_MEDIAN=4.31034e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.23508e-03;DP_MEDIAN=24;AF_Female=1.46399e-04;GQ_HIST_ALT=1|0|1|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|2|19;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.85325e-01;Hom_AMR=0;AC_EAS=1;AC_Female=16;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.00601e-05;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=12;AC_AFR=8;Hom_SAS=0;AC_ASJ=12;AF_raw=1.01514e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:4.95e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=A:0,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:4.501e-05,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0,EUR_MAF=A:0.001,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000258960,Consequence=3_prime_UTR_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=A:0.0002,Allele=A,IMPACT=MODIFIER,EXON=12/12,ExAC_AMR_MAF=A:0.0001927,cDNA_position=1551,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs371753337,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:4.942e-05,HGVSc=ENST00000258960.2:c.*42G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	inframe_deletion	134	137	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-19;AF_OTH=0.00000e+00;alleles=TACA%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63922e-05;Hom=0;AF_POPMAX=2.63817e-04;AN_POPMAX=15162;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24225e-05;AF_AFR=2.63817e-04;AC_raw=4;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07243e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.21158e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=4;AC_AFR=4;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=-:3.614e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=-:0,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=-:0,AFR_MAF=-:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=2,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=-:0,ENSP=ENSP00000258960,Consequence=inframe_deletion,Amino_acids=YN/Y,HGVSp=ENSP00000258960.2:p.Asn42del,STRAND=1,ExAC_SAS_MAF=-:0,CCDS=CCDS11494.1,EA_MAF=-:0.0007,Allele=-,IMPACT=MODERATE,EXON=1/12,ExAC_AMR_MAF=-:0.0004244,cDNA_position=140-142,CDS_position=122-124,ExAC_NFE_MAF=-:0,SYMBOL=NMT1,Existing_variation=rs766213031,VARIANT_CLASS=deletion,Protein_position=41-42,Codons=tACAac/tac,MINIMISED=1,ExAC_AFR_MAF=-:3.295e-05,HGVSc=ENST00000258960.2:c.124_126delAAC,ExAC_Adj_MAF=-:0
CDS|ENST00000258960	VCF	splice_region_variant	142	142	0.0	.	.	AC_Male=4;AF_NFE=2.73010e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25597e-29;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.64955e-05;Hom=0;AF_POPMAX=6.65513e-05;AN_POPMAX=15026;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=3.00680e-05;AF_AFR=6.65513e-05;AC_raw=4;AB_MEDIAN=5.27778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.27137e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62425e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:9.22e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=C:0.0001,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.668e-05,AFR_MAF=A:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=splice_region_variant&synonymous_variant,Amino_acids=R,HGVSp=ENST00000258960.2:c.129G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,EA_MAF=C:0,Allele=A,IMPACT=LOW,EXON=1/12,ExAC_AMR_MAF=A:0,cDNA_position=147,CDS_position=129,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs143955814,VARIANT_CLASS=SNV,Protein_position=43,Codons=cgG/cgA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.129G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	splice_region_variant	400	400	0.0	.	.	AC_Male=1;AF_NFE=8.98699e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.49763e-52;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13974e-06;Hom=0;AF_POPMAX=2.97992e-05;AN_POPMAX=33558;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43030e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.59152e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.29846e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.318e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=splice_region_variant&synonymous_variant,GMAF=A:0.0002,Amino_acids=G,HGVSp=ENST00000258960.2:c.387C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=T,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=405,CDS_position=387,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=129,AA_MAF=A:0,Codons=ggC/ggT,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.387C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	splice_region_variant	400	400	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=60;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.13501e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06987e-06;Hom=0;AF_POPMAX=6.53766e-05;AN_POPMAX=15296;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53766e-05;AC_raw=2;AB_MEDIAN=3.53758e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.07429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0000130275,ExAC_EAS_MAF=A:8.318e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,SWISSPROT=P30419,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000258960,Consequence=splice_region_variant&synonymous_variant,GMAF=A:0.0002,Amino_acids=G,HGVSp=ENST00000258960.2:c.387C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,CCDS=CCDS11494.1,Allele=A,IMPACT=LOW,EXON=4/12,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=405,CDS_position=387,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=129,AA_MAF=A:0,Codons=ggC/ggA,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000258960.2:c.387C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000258960	VCF	splice_region_variant	727	727	0.0	.	.	AC_Male=0;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07040e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.75083e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=301;AF_Female=9.00009e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.23711e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.3e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.507e-05,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF01233&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=splice_region_variant&synonymous_variant,Amino_acids=T,HGVSp=ENST00000258960.2:c.714A>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=LOW,EXON=7/12,ExAC_AMR_MAF=C:0,cDNA_position=732,CDS_position=714,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs752735481,VARIANT_CLASS=SNV,Protein_position=238,Codons=acA/acC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000258960.2:c.714A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000258960	VCF	splice_region_variant	1180	1180	0.0	.	.	AC_Male=26;AF_NFE=4.54298e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|7|24|25|20|7|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25657e-177;AF_OTH=1.85185e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=88;Hom_NFE=0;AF=3.61869e-04;Hom=1;AF_POPMAX=3.92567e-03;AN_POPMAX=15284;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|3|2|2|3|4|4|2|8|2|1|2|1|1|1|0|2|0;AF_Male=1.95298e-04;AF_AFR=3.92567e-03;AC_raw=89;AB_MEDIAN=4.71698e-01;Hom_EAS=0;AC_AMR=19;AF_ASJ=2.09380e-04;DP_MEDIAN=124;AF_Female=5.63370e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|88;Hom_raw=1;AF_SAS=3.29707e-05;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=62;Hom_AFR=1;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=60;AC_AFR=60;Hom_SAS=0;AC_ASJ=2;AF_raw=3.61392e-04;Hom_Female=1;AF_AMR=5.71738e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,PHENO=0&1,ExAC_EAS_MAF=T:0.000468,TREMBL=Q9Y465&Q96HI4&K7EN82,ExAC_MAF=T:0.0005,Feature=ENST00000258960,BIOTYPE=protein_coding,AMR_MAF=T:0.0061,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:6.085e-05,AFR_MAF=T:0,SWISSPROT=P30419,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=Gene3D:3.40.630.30&Pfam_domain:PF02799&PIRSF_domain:PIRSF015892&hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=splice_region_variant&synonymous_variant,GMAF=T:0.0016,Amino_acids=N,HGVSp=ENST00000258960.2:c.1167C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0.001152,CCDS=CCDS11494.1,EA_MAF=T:0.0054,SOMATIC=0&1,Allele=T,IMPACT=LOW,EXON=10/12,ExAC_AMR_MAF=T:0.004244,cDNA_position=1185,CDS_position=1167,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs142226258&COSM1383765,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=389,AA_MAF=T:0,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:4.612e-04,HGVSc=ENST00000258960.2:c.1167C>T,ExAC_Adj_MAF=T:0.0005195
CDS|ENST00000258960	VCF	5_prime_UTR_variant	1	1	0.0	.	.	AC_Male=1;AF_NFE=1.81683e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97631e-35;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.22423e-06;Hom=0;AF_POPMAX=1.81683e-05;AN_POPMAX=110082;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49704e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.69388e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.10763e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.64758e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:8.796e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.588e-05,AFR_MAF=T:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=6,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749106795,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000258960.2:c.-13C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	5_prime_UTR_variant	3	3	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-25;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.22037e-06;Hom=0;AF_POPMAX=6.52827e-05;AN_POPMAX=30636;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.49894e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.52827e-05;AS_RF=7.90407e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=T:1.756e-05,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0001323,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000258960,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,CCDS=CCDS11494.1,Allele=T,IMPACT=MODIFIER,EXON=1/12,ExAC_AMR_MAF=T:0,cDNA_position=8,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs768521050,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000258960.2:c.-11C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000258960	VCF	5_prime_UTR_variant	4	4	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-28;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10971e-06;Hom=0;AF_POPMAX=3.26456e-05;AN_POPMAX=30632;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49221e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.26316e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.26456e-05;AS_RF=8.77261e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=1/12,cDNA_position=9,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000258960.2:c.-10G>C
CDS|ENST00000258960	VCF	5_prime_UTR_variant	9	9	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-38;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09396e-06;Hom=0;AF_POPMAX=3.25797e-05;AN_POPMAX=30694;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46425e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25797e-05;AS_RF=8.95290e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=G:8.698e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000258960,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,CCDS=CCDS11494.1,Allele=G,IMPACT=MODIFIER,EXON=1/12,ExAC_AMR_MAF=G:0,cDNA_position=14,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774460908,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000258960.2:c.-5T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000258960	VCF	5_prime_UTR_variant	11	11	0.0	.	.	AC_Male=0;AF_NFE=9.03653e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-42;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.18371e-06;Hom=0;AF_POPMAX=3.00282e-05;AN_POPMAX=33302;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.85556e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.81238e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.38885e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=3.00282e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0000130275,ExAC_EAS_MAF=C:8.678e-06,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,SWISSPROT=P30419,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000258960,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0,CCDS=CCDS11494.1,Allele=C,IMPACT=MODIFIER,EXON=1/12,ExAC_AMR_MAF=C:0,cDNA_position=16,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs748067291,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000258960.2:c.-3A>C,ExAC_Adj_MAF=C:8.983e-05
CDS|ENST00000258960	VCF	5_prime_UTR_variant	13	13	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=13;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.77267e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.86832e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000258960,UNIPARC=UPI0000130275,Consequence=5_prime_UTR_variant,TREMBL=Q9Y465&Q96HI4&K7EN82,Feature=ENST00000258960,STRAND=1,BIOTYPE=protein_coding,CCDS=CCDS11494.1,Allele=A,IMPACT=MODIFIER,EXON=1/12,cDNA_position=18,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,SWISSPROT=P30419,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000258960.2:c.-1G>A
CDS|ENST00000543908	VCF	inframe_insertion	73	73	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-72;AF_OTH=1.82548e-04;alleles=A%2CAGGGAAC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07030e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42611e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.09091e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.02292e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=14,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=inframe_insertion&NMD_transcript_variant,Amino_acids=-/GN,HGVSp=ENSP00000439263.1:p.Asn25_Gly26dup,STRAND=1,Allele=GGGAAC,IMPACT=MODERATE,EXON=1/6,cDNA_position=73-74,CDS_position=63-64,SYMBOL=NMT1,VARIANT_CLASS=insertion,Protein_position=21-22,Codons=-/GGGAAC,MINIMISED=1,HGVSc=ENST00000543908.1:c.72_77dupGAACGG
CDS|ENST00000543908	VCF	inframe_insertion	83	83	0.0	.	.	AC_Male=5;AF_NFE=5.38871e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|2|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=5.01187e-60;AF_OTH=0.00000e+00;alleles=A%2CAACGGCC;AF_FIN=4.48994e-05;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84877e-05;Hom=0;AF_POPMAX=5.38871e-05;AN_POPMAX=111344;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|2|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=3.71261e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=3.80952e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80109e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.11301e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84241e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=ACGGCC:2.556e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=ACGGCC:4.635e-05,AFR_MAF=ACGGCC:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=ACGGCC:0,ENSP=ENSP00000439263,Consequence=inframe_insertion&NMD_transcript_variant,Amino_acids=N/NGH,HGVSp=ENSP00000439263.1:p.Gly26_His27dup,STRAND=1,ExAC_SAS_MAF=ACGGCC:0,Allele=ACGGCC,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=ACGGCC:0,cDNA_position=83-84,CDS_position=73-74,ExAC_NFE_MAF=ACGGCC:0,SYMBOL=NMT1,Existing_variation=rs763191382,VARIANT_CLASS=insertion,Protein_position=25,Codons=aac/aACGGCCac,MINIMISED=1,ExAC_AFR_MAF=ACGGCC:2.471e-05,HGVSc=ENST00000543908.1:c.75_80dupCGGCCA,ExAC_Adj_MAF=ACGGCC:0
CDS|ENST00000543908	VCF	synonymous_variant	28	28	0.0	.	.	AC_Male=3;AF_NFE=3.60536e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|3|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00010e-44;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44872e-05;Hom=0;AF_POPMAX=5.96516e-05;AN_POPMAX=33528;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|2|1|0|0|0|1|0|0|0|0|0|0;AF_Male=2.23125e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.54132e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=2.71316e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43635e-05;Hom_Female=0;AF_AMR=5.96516e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:3.427e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:6.219e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000543908.1:c.18G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=28,CDS_position=18,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs776210749,VARIANT_CLASS=SNV,Protein_position=6,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000543908.1:c.18G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	synonymous_variant	34	34	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16473e-06;Hom=0;AF_POPMAX=6.50407e-05;AN_POPMAX=30750;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43837e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=6.00160e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50407e-05;AS_RF=9.41280e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=A,HGVSp=ENST00000543908.1:c.24A>G(p.%253D),STRAND=1,Allele=G,IMPACT=LOW,EXON=1/6,cDNA_position=34,CDS_position=24,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=gcA/gcG,HGVSc=ENST00000543908.1:c.24A>G
CDS|ENST00000543908	VCF	synonymous_variant	34	34	0.0	.	.	AC_Male=0;AF_NFE=9.01534e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-23;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08237e-06;Hom=0;AF_POPMAX=9.01534e-06;AN_POPMAX=110922;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.51046e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=A,HGVSp=ENST00000543908.1:c.24A>C(p.%253D),STRAND=1,Allele=C,IMPACT=LOW,EXON=1/6,cDNA_position=34,CDS_position=24,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=gcA/gcC,HGVSc=ENST00000543908.1:c.24A>C
CDS|ENST00000543908	VCF	synonymous_variant	40	40	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-133;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08523e-06;Hom=0;AF_POPMAX=3.25373e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.44225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.78313e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=83;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25373e-05;AS_RF=8.78960e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.561e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=K,HGVSp=ENST00000543908.1:c.30G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=40,CDS_position=30,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs757761311,VARIANT_CLASS=SNV,Protein_position=10,Codons=aaG/aaA,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000543908.1:c.30G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	synonymous_variant	46	46	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-56;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16067e-06;Hom=0;AF_POPMAX=6.50745e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48723e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.23810e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50745e-05;AS_RF=8.94107e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.542e-06&C:8.542e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0&C:1.55e-05,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&C:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=P,HGVSp=ENST00000543908.1:c.36G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&C:0,Allele=T,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=T:0&C:0,cDNA_position=46,CDS_position=36,ExAC_NFE_MAF=T:0&C:0,SYMBOL=NMT1,Existing_variation=rs780444510,VARIANT_CLASS=SNV,Protein_position=12,Codons=ccG/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06&C:8.237e-06,HGVSc=ENST00000543908.1:c.36G>T,ExAC_Adj_MAF=T:0&C:0
CDS|ENST00000543908	VCF	synonymous_variant	56	56	0.0	.	.	AC_Male=1;AF_NFE=2.69721e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-37;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22188e-05;Hom=0;AF_POPMAX=2.69721e-05;AN_POPMAX=111226;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.42843e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.80333e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97663e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.515e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.545e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=L,HGVSp=ENST00000543908.1:c.46C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=56,CDS_position=46,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs748150811,VARIANT_CLASS=SNV,Protein_position=16,Codons=Ctg/Ttg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.46C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	synonymous_variant	64	64	0.0	.	.	AC_Male=0;AF_NFE=8.98828e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-59;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07106e-06;Hom=0;AF_POPMAX=8.98828e-06;AN_POPMAX=111256;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.77273e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00982e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05614e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=Q,HGVSp=ENST00000543908.1:c.54G>A(p.%253D),STRAND=1,Allele=A,IMPACT=LOW,EXON=1/6,cDNA_position=64,CDS_position=54,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=18,Codons=caG/caA,MINIMISED=1,HGVSc=ENST00000543908.1:c.54G>A
CDS|ENST00000543908	VCF	synonymous_variant	109	109	0.0	.	.	AC_Male=0;AF_NFE=9.00236e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.84034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07857e-06;Hom=0;AF_POPMAX=9.00236e-06;AN_POPMAX=111082;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.63736e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=13;AF_Female=9.02543e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.58906e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.666e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.57e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=C,HGVSp=ENST00000543908.1:c.99C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=109,CDS_position=99,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs762294220,VARIANT_CLASS=SNV,Protein_position=33,Codons=tgC/tgT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.99C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	synonymous_variant	112	112	0.0	.	.	AC_Male=0;AF_NFE=1.80050e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-23;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15614e-06;Hom=0;AF_POPMAX=1.80050e-05;AN_POPMAX=111080;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.76923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=1.80473e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.41561e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:1.741e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.152e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000543908.1:c.102G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=112,CDS_position=102,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768076232,VARIANT_CLASS=SNV,Protein_position=34,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000543908.1:c.102G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	synonymous_variant	121	121	0.0	.	.	AC_Male=0;AF_NFE=9.01567e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.22517e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08407e-06;Hom=0;AF_POPMAX=9.01567e-06;AN_POPMAX=110918;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.97806e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.57456e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000543908.1:c.111G>A(p.%253D),STRAND=1,Allele=A,IMPACT=LOW,EXON=1/6,cDNA_position=121,CDS_position=111,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=37,Codons=gaG/gaA,MINIMISED=1,HGVSc=ENST00000543908.1:c.111G>A
CDS|ENST00000543908	VCF	synonymous_variant	130	130	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-88;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=1.02270e-04;AN_POPMAX=9778;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.40984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.02270e-04;DP_MEDIAN=61;AF_Female=9.06914e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.25490e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:9.018e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=S,HGVSp=ENST00000543908.1:c.120C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,Allele=T,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=130,CDS_position=120,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=40,Codons=agC/agT,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.120C>T,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	synonymous_variant	136	136	0.0	.	.	AC_Male=9;AF_NFE=7.26388e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|1|0|3|1|2|2|4|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-29;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.75899e-05;Hom=0;AF_POPMAX=9.84252e-05;AN_POPMAX=30480;AC_NFE=8;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|3|2|2|6|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=6.75017e-05;AF_AFR=0.00000e+00;AC_raw=15;AB_MEDIAN=4.19355e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=4.55506e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|13;Hom_raw=0;AF_SAS=9.84252e-05;AS_RF=9.10989e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=9.08540e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:0.0001008,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001161,AFR_MAF=T:0.0001995,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=N,HGVSp=ENST00000543908.1:c.126C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=136,CDS_position=126,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766535198,VARIANT_CLASS=SNV,Protein_position=42,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:9.060e-05,HGVSc=ENST00000543908.1:c.126C>T,ExAC_Adj_MAF=T:9.878e-05
CDS|ENST00000543908	VCF	synonymous_variant	151	151	0.0	.	.	AC_Male=148;AF_NFE=1.34979e-03;Hom_FIN=0;GQ_MEDIAN=80;AB_HIST_ALT=0|0|4|13|34|85|90|44|24|6|1|2|0|0|1|0|0|0|0|0;AC_FIN=74;DREF_MEDIAN=1.00000e-08;AF_OTH=1.30939e-03;alleles=T%2CC;AF_FIN=3.42910e-03;AC_OTH=7;Hom_Male=0;AC=275;Hom_NFE=0;AF=1.14690e-03;Hom=0;AF_POPMAX=3.42910e-03;AN_POPMAX=21580;AC_NFE=145;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|5|4|20|31|38|39|37|27|29|22|24|7|6|3|2|2|0|1;AF_Male=1.12191e-03;AF_AFR=1.81476e-03;AC_raw=304;AB_MEDIAN=3.07692e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=1.23127e-03;DP_MEDIAN=42;AF_Female=1.17747e-03;GQ_HIST_ALT=4|4|6|8|5|9|8|12|6|14|13|6|13|13|19|10|18|17|12|107;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=5.26862e-02;Hom_AMR=0;AC_EAS=6;AC_Female=127;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.51206e-04;AC_SAS=0;POPMAX=FIN;AC_POPMAX=74;AC_AFR=27;Hom_SAS=0;AC_ASJ=12;AF_raw=1.24619e-03;Hom_Female=0;AF_AMR=1.20409e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:0.001857,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0.001923,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0.001052,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=S,HGVSp=ENST00000543908.1:c.141T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0.005814,Allele=C,IMPACT=LOW,EXON=2/6,ExAC_AMR_MAF=C:0.001447,cDNA_position=151,CDS_position=141,ExAC_NFE_MAF=C:0.01002,SYMBOL=NMT1,Existing_variation=rs777402320,VARIANT_CLASS=SNV,Protein_position=47,Codons=agT/agC,MINIMISED=1,ExAC_AFR_MAF=C:1.911e-03,HGVSc=ENST00000543908.1:c.141T>C,ExAC_Adj_MAF=C:0.000438
CDS|ENST00000543908	VCF	synonymous_variant	211	211	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|1|2|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.10793e-31;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.78394e-05;Hom=0;AF_POPMAX=3.99467e-04;AN_POPMAX=15020;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|1|2|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.68939e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.91379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=4.11794e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.74988e-01;Hom_AMR=0;AC_EAS=6;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.99467e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.46164e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:6.366e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=G:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,EAS_MAF=G:0,EUR_MAF=G:0.003,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.001103,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,GMAF=G:0.0006,Amino_acids=K,HGVSp=ENST00000543908.1:c.201A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=LOW,EXON=2/6,ExAC_AMR_MAF=G:0,cDNA_position=211,CDS_position=201,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs141656657,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=67,AA_MAF=G:0,Codons=aaA/aaG,MINIMISED=1,ExAC_AFR_MAF=G:3.314e-05,HGVSc=ENST00000543908.1:c.201A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	synonymous_variant	214	214	0.0	.	.	AC_Male=0;AF_NFE=1.12471e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.76844e-06;Hom=0;AF_POPMAX=1.12471e-05;AN_POPMAX=88912;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.05753e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.93464e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10344e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=G,HGVSp=ENST00000543908.1:c.204C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=2/6,cDNA_position=214,CDS_position=204,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=68,Codons=ggC/ggT,MINIMISED=1,HGVSc=ENST00000543908.1:c.204C>T
CDS|ENST00000543908	VCF	synonymous_variant	220	220	0.0	.	.	AC_Male=6;AF_NFE=8.41548e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|2|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15518e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=3.50814e-05;Hom=0;AF_POPMAX=8.41548e-05;AN_POPMAX=83180;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|1|0|2|1|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=5.48296e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.21637e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.10980e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12023e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.28394e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:5.723e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001152,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000543908.1:c.210G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=2/6,ExAC_AMR_MAF=A:0,cDNA_position=220,CDS_position=210,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs369434915,VARIANT_CLASS=SNV,Protein_position=70,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:2.496e-05,HGVSc=ENST00000543908.1:c.210G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	synonymous_variant	232	232	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-83;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.48408e-06;Hom=0;AF_POPMAX=9.03506e-05;AN_POPMAX=11068;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=9.03506e-05;AC_raw=1;AB_MEDIAN=6.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.21150e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.96517e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:2.3e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=T:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,GMAF=T:0.0002,Amino_acids=A,HGVSp=ENST00000543908.1:c.222C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=2/6,ExAC_AMR_MAF=T:0.0002112,cDNA_position=232,CDS_position=222,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs184508172,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=74,AA_MAF=T:0,Codons=gcC/gcT,MINIMISED=1,ExAC_AFR_MAF=T:8.398e-06,HGVSc=ENST00000543908.1:c.222C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	synonymous_variant	259	259	0.0	.	.	AC_Male=0;AF_NFE=9.11594e-06;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15014e-06;Hom=0;AF_POPMAX=9.11594e-06;AN_POPMAX=109698;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.77778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=9.19912e-06;GQ_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.62962e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.372e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.518e-05,AFR_MAF=C:0,EAS_MAF=C:0,EUR_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,GMAF=C:0.0002,Amino_acids=S,HGVSp=ENST00000543908.1:c.249T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=LOW,EXON=3/6,ExAC_AMR_MAF=C:0,cDNA_position=259,CDS_position=249,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs200633656,SAS_MAF=C:0.001,VARIANT_CLASS=SNV,Protein_position=83,AA_MAF=C:0,Codons=tcT/tcC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.249T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	synonymous_variant	283	283	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|2|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22868e-05;Hom=0;AF_POPMAX=9.08045e-05;AN_POPMAX=33038;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46949e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=6.81818e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.81347e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.72461e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=9.08045e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000543908.1:c.273A>G(p.%253D),STRAND=1,Allele=G,IMPACT=LOW,EXON=3/6,cDNA_position=283,CDS_position=273,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=91,Codons=gaA/gaG,MINIMISED=1,HGVSc=ENST00000543908.1:c.273A>G
CDS|ENST00000543908	VCF	synonymous_variant	298	298	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-142;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07917e-06;Hom=0;AF_POPMAX=6.55996e-05;AN_POPMAX=15244;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=6.55996e-05;AC_raw=1;AB_MEDIAN=4.83146e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.02657e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.95139e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.272e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=C:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=I,HGVSp=ENST00000543908.1:c.288T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,EA_MAF=C:0.0002,Allele=C,IMPACT=LOW,EXON=3/6,ExAC_AMR_MAF=C:9.641e-05,cDNA_position=298,CDS_position=288,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs372318247,VARIANT_CLASS=SNV,Protein_position=96,Codons=atT/atC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.288T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	synonymous_variant	304	304	0.0	.	.	AC_Male=1;AF_NFE=8.97747e-06;Hom_FIN=0;GQ_MEDIAN=73;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97611e-06;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14538e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.54779e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.00868e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.44770e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.266e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=L,HGVSp=ENST00000543908.1:c.294G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=3/6,ExAC_AMR_MAF=T:0,cDNA_position=304,CDS_position=294,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754577624,VARIANT_CLASS=SNV,Protein_position=98,Codons=ctG/ctT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.294G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	synonymous_variant	310	310	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07193e-06;Hom=0;AF_POPMAX=3.25457e-05;AN_POPMAX=30726;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43141e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25457e-05;AS_RF=8.52320e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=S,HGVSp=ENST00000543908.1:c.300A>G(p.%253D),STRAND=1,Allele=G,IMPACT=LOW,EXON=3/6,cDNA_position=310,CDS_position=300,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=100,Codons=tcA/tcG,MINIMISED=1,HGVSc=ENST00000543908.1:c.300A>G
CDS|ENST00000543908	VCF	synonymous_variant	322	322	0.0	.	.	AC_Male=1;AF_NFE=8.99006e-06;Hom_FIN=0;GQ_MEDIAN=34;AB_HIST_ALT=0|0|0|0|4|3|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=4.08532e-04;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=1.35404e-04;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44760e-05;Hom=0;AF_POPMAX=1.35404e-04;AN_POPMAX=22156;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.44114e-06;AF_AFR=1.31406e-04;AC_raw=8;AB_MEDIAN=2.47642e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=4.51467e-05;GQ_HIST_ALT=0|1|1|0|0|1|1|1|0|0|1|0|1|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.54316e-03;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:6.621e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:6.02e-05,AFR_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=G,HGVSp=ENST00000543908.1:c.312A>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=LOW,EXON=3/6,ExAC_AMR_MAF=C:0.0002899,cDNA_position=322,CDS_position=312,ExAC_NFE_MAF=C:0.0001537,SYMBOL=NMT1,Existing_variation=rs746348189,VARIANT_CLASS=SNV,Protein_position=104,Codons=ggA/ggC,MINIMISED=1,ExAC_AFR_MAF=C:9.060e-05,HGVSc=ENST00000543908.1:c.312A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	synonymous_variant	328	328	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07701e-06;Hom=0;AF_POPMAX=3.25945e-05;AN_POPMAX=30680;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25945e-05;AS_RF=8.53172e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=A,HGVSp=ENST00000543908.1:c.318C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/6,cDNA_position=328,CDS_position=318,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=106,Codons=gcC/gcT,MINIMISED=1,HGVSc=ENST00000543908.1:c.318C>T
CDS|ENST00000543908	VCF	synonymous_variant	346	346	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-42;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07501e-06;Hom=0;AF_POPMAX=2.99419e-05;AN_POPMAX=33398;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43450e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.92593e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.81783e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99419e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=A,HGVSp=ENST00000543908.1:c.336T>C(p.%253D),STRAND=1,Allele=C,IMPACT=LOW,EXON=3/6,cDNA_position=346,CDS_position=336,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=112,Codons=gcT/gcC,MINIMISED=1,HGVSc=ENST00000543908.1:c.336T>C
CDS|ENST00000543908	VCF	synonymous_variant	349	349	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07465e-06;Hom=0;AF_POPMAX=2.99455e-05;AN_POPMAX=33394;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.67568e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=37;AF_Female=9.01518e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92008e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99455e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=S,HGVSp=ENST00000543908.1:c.339C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/6,cDNA_position=349,CDS_position=339,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=113,Codons=agC/agT,MINIMISED=1,HGVSc=ENST00000543908.1:c.339C>T
CDS|ENST00000543908	VCF	synonymous_variant	367	367	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=25;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15231e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=8;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66799e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=F,HGVSp=ENST00000543908.1:c.357C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/6,cDNA_position=367,CDS_position=357,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=119,Codons=ttC/ttT,MINIMISED=1,HGVSc=ENST00000543908.1:c.357C>T
CDS|ENST00000543908	VCF	synonymous_variant	376	376	0.0	.	.	AC_Male=0;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-30;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.78261e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=9.08364e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.39564e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=T,HGVSp=ENST00000543908.1:c.366G>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/6,cDNA_position=376,CDS_position=366,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=122,Codons=acG/acT,HGVSc=ENST00000543908.1:c.366G>T
CDS|ENST00000543908	VCF	synonymous_variant	376	376	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|1|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.69441e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=3.02810e-05;AN_POPMAX=33024;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|3|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48671e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=1.60256e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.95538e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=3.02810e-05;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=T,HGVSp=ENST00000543908.1:c.366G>A(p.%253D),STRAND=1,Allele=A,IMPACT=LOW,EXON=3/6,cDNA_position=376,CDS_position=366,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=122,Codons=acG/acA,HGVSc=ENST00000543908.1:c.366G>A
CDS|ENST00000543908	VCF	synonymous_variant	382	382	0.0	.	.	AC_Male=13;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|2|0|5|2|0|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=15;Hom_NFE=0;AF=6.19001e-05;Hom=0;AF_POPMAX=4.28788e-04;AN_POPMAX=30318;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|4|2|1|1|1|0|1|0|0|2|1|0|0|1|0|0;AF_Male=9.78076e-05;AF_AFR=6.60153e-05;AC_raw=15;AB_MEDIAN=4.72797e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.82795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|15;Hom_raw=0;AF_SAS=4.28788e-04;AS_RF=9.33794e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.89692e-05;AC_SAS=13;POPMAX=SAS;AC_POPMAX=13;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09088e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.385e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0005311,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=P,HGVSp=ENST00000543908.1:c.372C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=3/6,ExAC_AMR_MAF=T:9.632e-05,cDNA_position=382,CDS_position=372,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs774578466,VARIANT_CLASS=SNV,Protein_position=124,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-05,HGVSc=ENST00000543908.1:c.372C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	synonymous_variant	388	388	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-31;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13839e-06;Hom=0;AF_POPMAX=3.31279e-05;AN_POPMAX=30186;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.54523e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.58333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.31279e-05;AS_RF=8.33412e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.422e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=P,HGVSp=ENST00000543908.1:c.378C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=LOW,EXON=3/6,ExAC_AMR_MAF=G:0,cDNA_position=388,CDS_position=378,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767261647,VARIANT_CLASS=SNV,Protein_position=126,Codons=ccC/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.378C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	15	15	0.0	.	.	AC_Male=0;AF_NFE=9.04748e-06;Hom_FIN=0;GQ_MEDIAN=20;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.90099e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.19363e-06;Hom=0;AF_POPMAX=3.00571e-05;AN_POPMAX=33270;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.81594e-05;GQ_HIST_ALT=0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.32038e-03;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=3.00571e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.651e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.997),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/V,HGVSp=ENSP00000439263.1:p.Ala2Val,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=15,CDS_position=5,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs771527303,VARIANT_CLASS=SNV,Protein_position=2,Codons=gCg/gTg,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000543908.1:c.5C>T,ExAC_Adj_MAF=T:8.965e-05
CDS|ENST00000543908	VCF	missense_variant	17	17	0.0	.	.	AC_Male=1;AF_NFE=9.02755e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-30;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.17307e-06;Hom=0;AF_POPMAX=6.58762e-05;AN_POPMAX=15180;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44923e-06;AF_AFR=6.58762e-05;AC_raw=2;AB_MEDIAN=4.35484e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=9.05272e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20566e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.622e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.564e-05,AFR_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.673),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=D/H,HGVSp=ENSP00000439263.1:p.Asp3His,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=C:0,cDNA_position=17,CDS_position=7,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs772761859,VARIANT_CLASS=SNV,Protein_position=3,Codons=Gac/Cac,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000543908.1:c.7G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	missense_variant	20	20	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16887e-06;Hom=0;AF_POPMAX=6.51339e-05;AN_POPMAX=30706;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=1.80973e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.51339e-05;AS_RF=9.34226e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.162),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=E/K,HGVSp=ENSP00000439263.1:p.Glu4Lys,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=1/6,cDNA_position=20,CDS_position=10,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=4,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000543908.1:c.10G>A
CDS|ENST00000543908	VCF	missense_variant	21	21	0.0	.	.	AC_Male=0;AF_NFE=9.01990e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08360e-06;Hom=0;AF_POPMAX=9.01990e-06;AN_POPMAX=110866;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=9.04732e-06;GQ_HIST_ALT=0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17447e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.595e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.559e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.154),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=E/G,HGVSp=ENSP00000439263.1:p.Glu4Gly,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=21,CDS_position=11,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs760309598,VARIANT_CLASS=SNV,Protein_position=4,Codons=gAg/gGg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000543908.1:c.11A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	23	23	0.0	.	.	AC_Male=31;AF_NFE=9.01518e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|4|2|10|15|9|8|6|1|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.15479e-38;AF_OTH=3.66838e-04;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=56;Hom_NFE=0;AF=2.28573e-04;Hom=0;AF_POPMAX=3.07603e-03;AN_POPMAX=17230;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|3|15|10|7|8|3|3|1|4|1|1|0|0|0|0|0|0;AF_Male=2.30614e-04;AF_AFR=0.00000e+00;AC_raw=56;AB_MEDIAN=4.76557e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=2.26093e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|56;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.34281e-01;Hom_AMR=0;AC_EAS=53;AC_Female=25;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.07603e-03;AC_SAS=0;POPMAX=EAS;AC_POPMAX=53;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.27391e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.14),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:0.0002232,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,EAS_MAF=C:0,EUR_MAF=C:0.001,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.015),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0.002947,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,GMAF=C:0.0002,Amino_acids=S/R,HGVSp=ENSP00000439263.1:p.Ser5Arg,STRAND=1,ExAC_SAS_MAF=C:0.001171,Allele=C,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=C:0,cDNA_position=23,CDS_position=13,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs564172691,SAS_MAF=C:0,VARIANT_CLASS=SNV,Protein_position=5,AA_MAF=C:0,Codons=Agt/Cgt,MINIMISED=1,ExAC_AFR_MAF=C:2.142e-04,HGVSc=ENST00000543908.1:c.13A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	missense_variant	24	24	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08090e-06;Hom=0;AF_POPMAX=3.25330e-05;AN_POPMAX=30738;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43760e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25330e-05;AS_RF=8.76833e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.74),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.025),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/N,HGVSp=ENSP00000439263.1:p.Ser5Asn,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=1/6,cDNA_position=24,CDS_position=14,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=5,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000543908.1:c.14G>A
CDS|ENST00000543908	VCF	missense_variant	29	29	0.0	.	.	AC_Male=0;AF_NFE=9.01372e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-34;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08110e-06;Hom=0;AF_POPMAX=9.01372e-06;AN_POPMAX=110942;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.80000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.04454e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06165e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.787),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=T/P,HGVSp=ENSP00000439263.1:p.Thr7Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/6,cDNA_position=29,CDS_position=19,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=7,Codons=Aca/Cca,MINIMISED=1,HGVSc=ENST00000543908.1:c.19A>C
CDS|ENST00000543908	VCF	missense_variant	32	32	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52365e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/T,HGVSp=ENSP00000439263.1:p.Ala8Thr,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=1/6,cDNA_position=32,CDS_position=22,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=Gca/Aca,HGVSc=ENST00000543908.1:c.22G>A
CDS|ENST00000543908	VCF	missense_variant	32	32	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-45;AF_OTH=1.83756e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08320e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.05108e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.37319e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.999),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/P,HGVSp=ENSP00000439263.1:p.Ala8Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/6,cDNA_position=32,CDS_position=22,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=8,Codons=Gca/Cca,HGVSc=ENST00000543908.1:c.22G>C
CDS|ENST00000543908	VCF	missense_variant	33	33	0.0	.	.	AC_Male=4;AF_NFE=9.02104e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-43;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63397e-05;Hom=0;AF_POPMAX=9.75864e-05;AN_POPMAX=30742;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=2.97699e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.70769e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=9.75864e-05;AS_RF=9.42769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:1.713e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.554e-05,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.997),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/V,HGVSp=ENSP00000439263.1:p.Ala8Val,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=33,CDS_position=23,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764406772,VARIANT_CLASS=SNV,Protein_position=8,Codons=gCa/gTa,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000543908.1:c.23C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	35	35	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-39;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08257e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=9.04846e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.15769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.21),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.556e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=V/L,HGVSp=ENSP00000439263.1:p.Val9Leu,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=C:0,cDNA_position=35,CDS_position=25,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs752105945,VARIANT_CLASS=SNV,Protein_position=9,Codons=Gtg/Ctg,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000543908.1:c.25G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	missense_variant	41	41	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.87339e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.62),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.554e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/S,HGVSp=ENSP00000439263.1:p.Pro11Ser,STRAND=1,ExAC_SAS_MAF=A:0,Allele=T,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=41,CDS_position=31,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=11,Codons=Ccg/Tcg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000543908.1:c.31C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	41	41	0.0	.	.	AC_Male=0;AF_NFE=9.02006e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38634e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08397e-06;Hom=0;AF_POPMAX=9.02006e-06;AN_POPMAX=110864;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.70833e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=18;AF_Female=9.05403e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.26525e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.32),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.554e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.025),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/T,HGVSp=ENSP00000439263.1:p.Pro11Thr,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=41,CDS_position=31,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=11,Codons=Ccg/Acg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000543908.1:c.31C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	42	42	0.0	.	.	AC_Male=2;AF_NFE=9.01664e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-48;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16573e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48792e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63469e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.40560e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.24),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.552e-05,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/L,HGVSp=ENSP00000439263.1:p.Pro11Leu,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=42,CDS_position=32,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs750513385,VARIANT_CLASS=SNV,Protein_position=11,Codons=cCg/cTg,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000543908.1:c.32C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	45	45	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=62;AB_HIST_ALT=0|0|2|0|0|2|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25280e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22474e-05;Hom=0;AF_POPMAX=6.50703e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|1|0|2|0|1|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44025e-06;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=1.80920e-05;GQ_HIST_ALT=1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.50703e-05;AS_RF=1.16160e-02;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=2.98401e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.34),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/L,HGVSp=ENSP00000439263.1:p.Pro12Leu,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=45,CDS_position=35,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=12,Codons=cCg/cTg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000543908.1:c.35C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	45	45	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=58;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.80083e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08247e-06;Hom=0;AF_POPMAX=3.25351e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.95563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=9.04601e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25351e-05;AS_RF=1.45870e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.24),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:1.71e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.548),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/Q,HGVSp=ENSP00000439263.1:p.Pro12Gln,STRAND=1,ExAC_SAS_MAF=T:0,Allele=A,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=45,CDS_position=35,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=12,Codons=cCg/cAg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000543908.1:c.35C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	47	47	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-63;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08007e-06;Hom=0;AF_POPMAX=5.80181e-05;AN_POPMAX=17236;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60976e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96821e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.09),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/P,HGVSp=ENSP00000439263.1:p.Ala13Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/6,cDNA_position=47,CDS_position=37,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=13,Codons=Gca/Cca,MINIMISED=1,HGVSc=ENST00000543908.1:c.37G>C
CDS|ENST00000543908	VCF	missense_variant	50	50	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97164e-32;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15627e-06;Hom=0;AF_POPMAX=1.16063e-04;AN_POPMAX=17232;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.57018e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80682e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52227e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.16063e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.25),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.534e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.696),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001174,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/S,HGVSp=ENSP00000439263.1:p.Pro14Ser,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=T:0,cDNA_position=50,CDS_position=40,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754859910,VARIANT_CLASS=SNV,Protein_position=14,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000543908.1:c.40C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	51	51	0.0	.	.	AC_Male=1;AF_NFE=2.69964e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.37387e-64;AF_OTH=1.83217e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63090e-05;Hom=0;AF_POPMAX=2.69964e-05;AN_POPMAX=111126;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.03446e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=2.70929e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36654e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.28),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.011),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/L,HGVSp=ENSP00000439263.1:p.Pro14Leu,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=1/6,cDNA_position=51,CDS_position=41,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=14,Codons=cCt/cTt,MINIMISED=1,HGVSc=ENST00000543908.1:c.41C>T
CDS|ENST00000543908	VCF	missense_variant	54	54	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-53;AF_OTH=1.83083e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22264e-05;Hom=0;AF_POPMAX=6.58068e-05;AN_POPMAX=15196;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43262e-06;AF_AFR=6.58068e-05;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=1.80460e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35197e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:1.705e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=T:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,EAS_MAF=T:0.0014,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.04),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,GMAF=T:0.0002,Amino_acids=P/L,HGVSp=ENSP00000439263.1:p.Pro15Leu,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=T:0.0001013,cDNA_position=54,CDS_position=44,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs202061902,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=15,AA_MAF=T:0,Codons=cCg/cTg,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000543908.1:c.44C>T,ExAC_Adj_MAF=T:8.969e-05
CDS|ENST00000543908	VCF	missense_variant	57	57	0.0	.	.	AC_Male=1;AF_NFE=8.98893e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-25;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07236e-06;Hom=0;AF_POPMAX=8.98893e-06;AN_POPMAX=111248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42765e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.62500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.89),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.703e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.089e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=L/R,HGVSp=ENSP00000439263.1:p.Leu16Arg,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=57,CDS_position=47,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772038652,VARIANT_CLASS=SNV,Protein_position=16,Codons=cTg/cGg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000543908.1:c.47T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	66	66	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-33;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14120e-06;Hom=0;AF_POPMAX=5.96019e-05;AN_POPMAX=33556;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42589e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.78231e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=5.96019e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.95),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=M/R,HGVSp=ENSP00000439263.1:p.Met19Arg,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=1/6,cDNA_position=66,CDS_position=56,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=19,Codons=aTg/aGg,HGVSc=ENST00000543908.1:c.56T>G
CDS|ENST00000543908	VCF	missense_variant	66	66	0.0	.	.	AC_Male=0;AF_NFE=8.98650e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-65;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07060e-06;Hom=0;AF_POPMAX=8.98650e-06;AN_POPMAX=111278;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43341e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.12),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.051),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=M/T,HGVSp=ENSP00000439263.1:p.Met19Thr,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/6,cDNA_position=66,CDS_position=56,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=19,Codons=aTg/aCg,HGVSc=ENST00000543908.1:c.56T>C
CDS|ENST00000543908	VCF	missense_variant	69	69	0.0	.	.	AC_Male=7;AF_NFE=9.88373e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|3|1|3|3|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-45;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.47784e-05;Hom=0;AF_POPMAX=9.88373e-05;AN_POPMAX=111294;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|4|0|1|0|2|0|1|0|1|0|0|0|0;AF_Male=5.19889e-05;AF_AFR=0.00000e+00;AC_raw=11;AB_MEDIAN=4.18860e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.60328e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=11;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.08),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:7.653e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0.0001388,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.037),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=M/R,HGVSp=ENSP00000439263.1:p.Met20Arg,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=69,CDS_position=59,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772952636,VARIANT_CLASS=SNV,Protein_position=20,Codons=aTg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:7.413e-05,HGVSc=ENST00000543908.1:c.59T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	80	80	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=52;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.20127e-01;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07090e-06;Hom=0;AF_POPMAX=2.98098e-05;AN_POPMAX=33546;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.16667e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.00836e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.23972e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=2.98098e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.12),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.52e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.526),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/R,HGVSp=ENSP00000439263.1:p.Gly24Arg,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=80,CDS_position=70,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746539074,VARIANT_CLASS=SNV,Protein_position=24,Codons=Ggg/Agg,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000543908.1:c.70G>A,ExAC_Adj_MAF=A:9.027e-05
CDS|ENST00000543908	VCF	missense_variant	81	81	0.0	.	.	AC_Male=1;AF_NFE=8.98182e-06;Hom_FIN=0;GQ_MEDIAN=54;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.54545e-02;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98182e-06;AN_POPMAX=111336;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42688e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.26923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.37827e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(1),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.173),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/A,HGVSp=ENSP00000439263.1:p.Gly24Ala,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/6,cDNA_position=81,CDS_position=71,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=24,Codons=gGg/gCg,MINIMISED=1,HGVSc=ENST00000543908.1:c.71G>C
CDS|ENST00000543908	VCF	missense_variant	86	86	0.0	.	.	AC_Male=0;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.53267e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07070e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.38095e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.00722e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.31156e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.39),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.529e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.546e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.012),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/S,HGVSp=ENSP00000439263.1:p.Gly26Ser,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=86,CDS_position=76,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs770300796,VARIANT_CLASS=SNV,Protein_position=26,Codons=Ggc/Agc,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000543908.1:c.76G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	91	91	0.0	.	.	AC_Male=1;AF_NFE=8.98101e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98101e-06;AN_POPMAX=111346;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42721e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.37664e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.539e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.547e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.835),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=H/Q,HGVSp=ENSP00000439263.1:p.His27Gln,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=91,CDS_position=81,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs776300314,VARIANT_CLASS=SNV,Protein_position=27,Codons=caT/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000543908.1:c.81T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	93	93	0.0	.	.	AC_Male=0;AF_NFE=8.98505e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.31688e-02;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07130e-06;Hom=0;AF_POPMAX=8.98505e-06;AN_POPMAX=111296;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.51984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.00690e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.21757e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI00019150A9,PHENO=1,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.167),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=E/V,HGVSp=ENSP00000439263.1:p.Glu28Val,STRAND=1,SOMATIC=1,Allele=T,IMPACT=MODERATE,EXON=1/6,cDNA_position=93,CDS_position=83,SYMBOL=NMT1,Existing_variation=COSM1128678,VARIANT_CLASS=SNV,Protein_position=28,Codons=gAg/gTg,MINIMISED=1,HGVSc=ENST00000543908.1:c.83A>T
CDS|ENST00000543908	VCF	missense_variant	97	97	0.0	.	.	AC_Male=0;AF_NFE=8.98957e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-73;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07286e-06;Hom=0;AF_POPMAX=8.98957e-06;AN_POPMAX=111240;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.37037e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=9.01128e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05502e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.571e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.553e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.835),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=H/Q,HGVSp=ENSP00000439263.1:p.His29Gln,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=97,CDS_position=87,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759161485,VARIANT_CLASS=SNV,Protein_position=29,Codons=caC/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000543908.1:c.87C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	99	99	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-32;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07425e-06;Hom=0;AF_POPMAX=5.80518e-05;AN_POPMAX=17226;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43362e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.34667e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80518e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.588e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001181,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=C/Y,HGVSp=ENSP00000439263.1:p.Cys30Tyr,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=99,CDS_position=89,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764495116,VARIANT_CLASS=SNV,Protein_position=30,Codons=tGc/tAc,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000543908.1:c.89G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	101	101	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-26;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22221e-05;Hom=0;AF_POPMAX=8.96111e-05;AN_POPMAX=33478;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43329e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.21053e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.80297e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.53191e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=8.96111e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.08),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.721e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.352),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/G,HGVSp=ENSP00000439263.1:p.Ser31Gly,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=101,CDS_position=91,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774684452,VARIANT_CLASS=SNV,Protein_position=31,Codons=Agc/Ggc,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000543908.1:c.91A>G,ExAC_Adj_MAF=G:0.0001836
CDS|ENST00000543908	VCF	missense_variant	130	130	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-29;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=3.26861e-05;AN_POPMAX=30594;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.47005e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.26861e-05;AS_RF=8.82577e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.06),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:9.018e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.483),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/R,HGVSp=ENSP00000439263.1:p.Ser40Arg,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=130,CDS_position=120,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=40,Codons=agC/agG,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.120C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	132	132	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92478e-20;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09799e-06;Hom=0;AF_POPMAX=5.83158e-05;AN_POPMAX=17148;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.91667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07293e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.95804e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.83158e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.06),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:9.058e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.614),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.0001227,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Y/C,HGVSp=ENSP00000439263.1:p.Tyr41Cys,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=132,CDS_position=122,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756247053,VARIANT_CLASS=SNV,Protein_position=41,Codons=tAc/tGc,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000543908.1:c.122A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	135	135	0.0	.	.	AC_Male=1;AF_NFE=9.07738e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-55;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.11265e-06;Hom=0;AF_POPMAX=9.07738e-06;AN_POPMAX=110164;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49805e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.29412e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.17479e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06068e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.53),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=N/S,HGVSp=ENSP00000439263.1:p.Asn42Ser,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=1/6,cDNA_position=135,CDS_position=125,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=42,Codons=aAc/aGc,MINIMISED=1,HGVSc=ENST00000543908.1:c.125A>G
CDS|ENST00000543908	VCF	missense_variant	138	138	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=7;AB_HIST_ALT=0|0|2|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.66338e-01;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=4.53227e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12712e-06;Hom=0;AF_POPMAX=4.53227e-05;AN_POPMAX=22064;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.52298e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.73728e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21819e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.03),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.619),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=R/P,HGVSp=ENSP00000439263.1:p.Arg43Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/6,cDNA_position=138,CDS_position=128,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=43,Codons=cGg/cCg,MINIMISED=1,HGVSc=ENST00000543908.1:c.128G>C
CDS|ENST00000543908	VCF	missense_variant	146	146	0.0	.	.	AC_Male=1;AF_NFE=9.20793e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-78;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13846e-06;Hom=0;AF_POPMAX=9.20793e-06;AN_POPMAX=108602;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.53477e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=50;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.26429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09934e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.09),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.304e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.508e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.077),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=L/V,HGVSp=ENSP00000439263.1:p.Leu46Val,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=G:0,cDNA_position=146,CDS_position=136,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs758247752,VARIANT_CLASS=SNV,Protein_position=46,Codons=Ttg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000543908.1:c.136T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	147	147	0.0	.	.	AC_Male=1;AF_NFE=9.20082e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-91;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13363e-06;Hom=0;AF_POPMAX=9.20082e-06;AN_POPMAX=108686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.52627e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.83900e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.898),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=L/W,HGVSp=ENSP00000439263.1:p.Leu46Trp,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=2/6,cDNA_position=147,CDS_position=137,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=46,Codons=tTg/tGg,MINIMISED=1,HGVSc=ENST00000543908.1:c.137T>G
CDS|ENST00000543908	VCF	missense_variant	150	150	0.0	.	.	AC_Male=1;AF_NFE=9.18628e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-41;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12361e-06;Hom=0;AF_POPMAX=9.18628e-06;AN_POPMAX=108858;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.50875e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.88840e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09927e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.91),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/N,HGVSp=ENSP00000439263.1:p.Ser47Asn,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=2/6,cDNA_position=150,CDS_position=140,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=47,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000543908.1:c.140G>A
CDS|ENST00000543908	VCF	missense_variant	152	152	0.0	.	.	AC_Male=0;AF_NFE=9.18577e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-80;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12368e-06;Hom=0;AF_POPMAX=9.18577e-06;AN_POPMAX=108864;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=9.14645e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40367e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.15),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.488),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/A,HGVSp=ENSP00000439263.1:p.Pro48Ala,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=2/6,cDNA_position=152,CDS_position=142,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=48,Codons=Cca/Gca,MINIMISED=1,HGVSc=ENST00000543908.1:c.142C>G
CDS|ENST00000543908	VCF	missense_variant	158	158	0.0	.	.	AC_Male=6;AF_NFE=4.58573e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|3|2|4|8|1|1|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-54;AF_OTH=1.83352e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=21;Hom_NFE=0;AF=8.63501e-05;Hom=0;AF_POPMAX=9.81804e-04;AN_POPMAX=15278;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|2|5|2|2|2|0|3|0|0|1|0|1|0|0|1;AF_Male=4.49384e-05;AF_AFR=9.81804e-04;AC_raw=21;AB_MEDIAN=5.21739e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=1.36761e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|21;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=15;AC_AFR=15;Hom_SAS=0;AC_ASJ=0;AF_raw=8.60860e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.9),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.336e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=G:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=G:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.034e-05,AFR_MAF=G:0,EAS_MAF=G:0,EUR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,GMAF=G:0.0002,Amino_acids=N/D,HGVSp=ENSP00000439263.1:p.Asn50Asp,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0.0011,Allele=G,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=G:0.000789,cDNA_position=158,CDS_position=148,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs140455291,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=50,AA_MAF=G:0,Codons=Aat/Gat,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-05,HGVSc=ENST00000543908.1:c.148A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	159	159	0.0	.	.	AC_Male=2;AF_NFE=5.50327e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.29463e-76;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.46765e-05;Hom=0;AF_POPMAX=5.50327e-05;AN_POPMAX=109026;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AF_Male=1.49817e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.64551e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=3.64797e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53507e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.45964e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.13),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:2.508e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:4.569e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.007),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=N/S,HGVSp=ENSP00000439263.1:p.Asn50Ser,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=G:0,cDNA_position=159,CDS_position=149,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs757177482,VARIANT_CLASS=SNV,Protein_position=50,Codons=aAt/aGt,MINIMISED=1,ExAC_AFR_MAF=G:2.471e-05,HGVSc=ENST00000543908.1:c.149A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	171	171	0.0	.	.	AC_Male=3;AF_NFE=4.59441e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|2|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-54;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.05744e-05;Hom=0;AF_POPMAX=4.59441e-05;AN_POPMAX=108828;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|2|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24908e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.80645e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.82428e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99531e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.04965e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:4.372e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.027e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/V,HGVSp=ENSP00000439263.1:p.Ala54Val,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=T:0,cDNA_position=171,CDS_position=161,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs780748535,VARIANT_CLASS=SNV,Protein_position=54,Codons=gCc/gTc,MINIMISED=1,ExAC_AFR_MAF=T:4.118e-05,HGVSc=ENST00000543908.1:c.161C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	174	174	0.0	.	.	AC_Male=6;AF_NFE=6.46365e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|1|0|3|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-50;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.88843e-05;Hom=0;AF_POPMAX=6.46365e-05;AN_POPMAX=108298;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|2|1|1|0|0|0|0|0|1|0|0|0|0;AF_Male=4.50857e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.32432e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=9.15198e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.86984e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.05),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.23),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/R,HGVSp=ENSP00000439263.1:p.Lys55Arg,STRAND=1,ExAC_SAS_MAF=T:0&G:0,Allele=G,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=T:0&G:0,cDNA_position=174,CDS_position=164,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=55,Codons=aAa/aGa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000543908.1:c.164A>G,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000543908	VCF	missense_variant	174	174	0.0	.	.	AC_Male=1;AF_NFE=9.23378e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-64;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12633e-06;Hom=0;AF_POPMAX=9.23378e-06;AN_POPMAX=108298;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.51428e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.22727e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09977e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.066),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/I,HGVSp=ENSP00000439263.1:p.Lys55Ile,STRAND=1,ExAC_SAS_MAF=T:0&G:0,Allele=T,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=T:0&G:0,cDNA_position=174,CDS_position=164,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=55,Codons=aAa/aTa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000543908.1:c.164A>T,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000543908	VCF	missense_variant	186	186	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-24;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15155e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.12500e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=9.21302e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=2.89217e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10004e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.274),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/R,HGVSp=ENSP00000439263.1:p.Lys59Arg,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=2/6,cDNA_position=186,CDS_position=176,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=59,Codons=aAg/aGg,MINIMISED=1,HGVSc=ENST00000543908.1:c.176A>G
CDS|ENST00000543908	VCF	missense_variant	203	203	0.0	.	.	AC_Male=0;AF_NFE=9.88807e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-130;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.33099e-06;Hom=0;AF_POPMAX=9.88807e-06;AN_POPMAX=101132;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.14563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=9.61908e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33183e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10129e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.1),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.315e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.529e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.168),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/E,HGVSp=ENSP00000439263.1:p.Lys65Glu,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=G:0,cDNA_position=203,CDS_position=193,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779784731,VARIANT_CLASS=SNV,Protein_position=65,Codons=Aaa/Gaa,MINIMISED=1,ExAC_AFR_MAF=G:8.261e-06,HGVSc=ENST00000543908.1:c.193A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	213	213	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30719e-25;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.87099e-05;Hom=0;AF_POPMAX=1.31596e-04;AN_POPMAX=30396;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.55437e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.49730e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.03795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66438e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64119e-05;Hom_Female=0;AF_AMR=1.31596e-04;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.241),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/V,HGVSp=ENSP00000439263.1:p.Gly68Val,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=2/6,cDNA_position=213,CDS_position=203,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=68,Codons=gGc/gTc,MINIMISED=1,HGVSc=ENST00000543908.1:c.203G>T
CDS|ENST00000543908	VCF	missense_variant	230	230	0.0	.	.	AC_Male=1;AF_NFE=2.58685e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-31;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.06140e-05;Hom=0;AF_POPMAX=2.58685e-05;AN_POPMAX=77314;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=9.69330e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.87363e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.17280e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.91480e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.21760e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.053),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/S,HGVSp=ENSP00000439263.1:p.Ala74Ser,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=2/6,cDNA_position=230,CDS_position=220,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=74,Codons=Gcc/Tcc,MINIMISED=1,HGVSc=ENST00000543908.1:c.220G>T
CDS|ENST00000543908	VCF	missense_variant	231	231	0.0	.	.	AC_Male=0;AF_NFE=1.30774e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.34920e-06;Hom=0;AF_POPMAX=1.30774e-05;AN_POPMAX=76468;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.84615e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=65;AF_Female=1.18189e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.26907e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10985e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.14),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/V,HGVSp=ENSP00000439263.1:p.Ala74Val,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=2/6,cDNA_position=231,CDS_position=221,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=74,Codons=gCc/gTc,MINIMISED=1,HGVSc=ENST00000543908.1:c.221C>T
CDS|ENST00000543908	VCF	missense_variant	235	235	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-72;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.55759e-06;Hom=0;AF_POPMAX=3.91972e-05;AN_POPMAX=25512;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.22730e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.91972e-05;AS_RF=8.51470e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11306e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.18),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.769),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Q/H,HGVSp=ENSP00000439263.1:p.Gln75His,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=2/6,cDNA_position=235,CDS_position=225,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=75,Codons=caG/caC,MINIMISED=1,HGVSc=ENST00000543908.1:c.225G>C
CDS|ENST00000543908	VCF	missense_variant	239	239	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=70;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97133e-05;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.12740e-05;Hom=0;AF_POPMAX=8.46453e-05;AN_POPMAX=11814;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.03086e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.94118e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=1.24387e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.04301e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=8.46453e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.23113e-06;Hom_Female=0;AF_AMR=3.93236e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.13),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.318),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Q/K,HGVSp=ENSP00000439263.1:p.Gln77Lys,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=2/6,cDNA_position=239,CDS_position=229,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=77,Codons=Cag/Aag,MINIMISED=1,HGVSc=ENST00000543908.1:c.229C>A
CDS|ENST00000543908	VCF	missense_variant	245	245	0.0	.	.	AC_Male=1;AF_NFE=2.98686e-05;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|2|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.19832e-05;Hom=0;AF_POPMAX=2.98686e-05;AN_POPMAX=66960;AC_NFE=2;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.09965e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.15047e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.31645e-05;GQ_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.22455e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64978e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:2.776e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:5.974e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.047),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=V/M,HGVSp=ENSP00000439263.1:p.Val79Met,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=2/6,ExAC_AMR_MAF=A:0,cDNA_position=245,CDS_position=235,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761306458,VARIANT_CLASS=SNV,Protein_position=79,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.569e-06,HGVSc=ENST00000543908.1:c.235G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	251	251	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-33;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.41163e-06;Hom=0;AF_POPMAX=6.76636e-05;AN_POPMAX=29558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.53130e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.32389e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.76636e-05;AS_RF=8.96351e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12123e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.75),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.681e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.000128,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&splice_region_variant&NMD_transcript_variant,Amino_acids=M/V,HGVSp=ENSP00000439263.1:p.Met81Val,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=G:0,cDNA_position=251,CDS_position=241,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767459577,VARIANT_CLASS=SNV,Protein_position=81,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000543908.1:c.241A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	255	255	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51591e-22;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.09459e-05;AN_POPMAX=16408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.23913e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20091e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.09459e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.06),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.391e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=T:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.017),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=N/T,HGVSp=ENSP00000439263.1:p.Asn82Thr,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=C,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=255,CDS_position=245,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=82,Codons=aAc/aCc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.245A>C,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	255	255	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-62;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.67646e-05;AN_POPMAX=14978;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.67646e-05;AC_raw=1;AB_MEDIAN=3.09859e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.02337e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.02),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.391e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=T:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.541),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=N/I,HGVSp=ENSP00000439263.1:p.Asn82Ile,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=255,CDS_position=245,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=82,Codons=aAc/aTc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.245A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	277	277	0.0	.	.	AC_Male=1;AF_NFE=9.04977e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-52;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10988e-06;Hom=0;AF_POPMAX=9.04977e-06;AN_POPMAX=110500;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49524e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.10256e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.90362e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.312e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.51e-05,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.013),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=I/M,HGVSp=ENSP00000439263.1:p.Ile89Met,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=G:0,cDNA_position=277,CDS_position=267,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779405921,VARIANT_CLASS=SNV,Protein_position=89,Codons=atC/atG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.267C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	296	296	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-21;AF_OTH=1.83554e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08013e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.70588e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=9.03130e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.67445e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.978),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=I/V,HGVSp=ENSP00000439263.1:p.Ile96Val,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=3/6,cDNA_position=296,CDS_position=286,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=96,Codons=Att/Gtt,MINIMISED=1,HGVSc=ENST00000543908.1:c.286A>G
CDS|ENST00000543908	VCF	missense_variant	312	312	0.0	.	.	AC_Male=0;AF_NFE=8.97263e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-62;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07163e-06;Hom=0;AF_POPMAX=8.97263e-06;AN_POPMAX=111450;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=48;AF_Female=9.00739e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.258e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=V/E,HGVSp=ENSP00000439263.1:p.Val101Glu,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=A:0,cDNA_position=312,CDS_position=302,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs778561485,VARIANT_CLASS=SNV,Protein_position=101,Codons=gTg/gAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.302T>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	314	314	0.0	.	.	AC_Male=0;AF_NFE=8.97167e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-66;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07073e-06;Hom=0;AF_POPMAX=8.97167e-06;AN_POPMAX=111462;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.45455e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00414e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97942e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.3),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.258e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(1),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/C,HGVSp=ENSP00000439263.1:p.Gly102Cys,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=T:0,cDNA_position=314,CDS_position=304,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs747390700,VARIANT_CLASS=SNV,Protein_position=102,Codons=Ggt/Tgt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.304G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	319	319	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-48;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07186e-06;Hom=0;AF_POPMAX=3.25563e-05;AN_POPMAX=30716;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43097e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25563e-05;AS_RF=9.07079e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.03),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.256e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.997),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Q/H,HGVSp=ENSP00000439263.1:p.Gln103His,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=C:0,cDNA_position=319,CDS_position=309,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs771371139,VARIANT_CLASS=SNV,Protein_position=103,Codons=caG/caC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.309G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	missense_variant	320	320	0.0	.	.	AC_Male=1;AF_NFE=8.97392e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07279e-06;Hom=0;AF_POPMAX=8.97392e-06;AN_POPMAX=111434;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43152e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.97872e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.42544e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.07),UNIPARC=UPI00019150A9,PHENO=0&1,ExAC_EAS_MAF=A:8.254e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(1),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,GMAF=A:0.0002,Amino_acids=G/R,HGVSp=ENSP00000439263.1:p.Gly104Arg,STRAND=1,ExAC_SAS_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=A:0,cDNA_position=320,CDS_position=310,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs563736659&COSM1493963,SAS_MAF=A:0.001,VARIANT_CLASS=SNV,Protein_position=104,AA_MAF=A:0,Codons=Gga/Aga,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.310G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	336	336	0.0	.	.	AC_Male=1;AF_NFE=8.98053e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-63;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07515e-06;Hom=0;AF_POPMAX=8.98053e-06;AN_POPMAX=111352;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43528e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.03846e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=52;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18859e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.249e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.501e-05,AFR_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.974),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=M/T,HGVSp=ENSP00000439263.1:p.Met109Thr,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=C:0,cDNA_position=336,CDS_position=326,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs770043528,VARIANT_CLASS=SNV,Protein_position=109,Codons=aTg/aCg,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.326T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	missense_variant	347	347	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=7.94328e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=4.48632e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07581e-06;Hom=0;AF_POPMAX=4.48632e-05;AN_POPMAX=22290;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43572e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.25000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.10681e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.11),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.215),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/G,HGVSp=ENSP00000439263.1:p.Ser113Gly,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=3/6,cDNA_position=347,CDS_position=337,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=113,Codons=Agc/Ggc,MINIMISED=1,HGVSc=ENST00000543908.1:c.337A>G
CDS|ENST00000543908	VCF	missense_variant	354	354	0.0	.	.	AC_Male=1;AF_NFE=1.79727e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-36;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15328e-06;Hom=0;AF_POPMAX=1.79727e-05;AN_POPMAX=111280;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=9.02120e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.61453e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI00019150A9,PHENO=0&1,ExAC_EAS_MAF=T:8.259e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=T:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=R/L,HGVSp=ENSP00000439263.1:p.Arg115Leu,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=T:0,cDNA_position=354,CDS_position=344,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs377156745&COSM436718,VARIANT_CLASS=SNV,Protein_position=115,Codons=cGa/cTa,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.344G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	356	356	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07525e-06;Hom=0;AF_POPMAX=3.25839e-05;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43550e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25839e-05;AS_RF=7.10677e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.33),UNIPARC=UPI00019150A9,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.997),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/R,HGVSp=ENSP00000439263.1:p.Ser116Arg,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=3/6,cDNA_position=356,CDS_position=346,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=116,Codons=Agc/Cgc,MINIMISED=1,HGVSc=ENST00000543908.1:c.346A>C
CDS|ENST00000543908	VCF	missense_variant	375	375	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.91433e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.37719e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.02383e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI00019150A9,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.999),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=T/M,HGVSp=ENSP00000439263.1:p.Thr122Met,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=T:0,cDNA_position=375,CDS_position=365,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=122,Codons=aCg/aTg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.365C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	375	375	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-14;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.51858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0),UNIPARC=UPI00019150A9,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.999),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=T/R,HGVSp=ENSP00000439263.1:p.Thr122Arg,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=G,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=T:0,cDNA_position=375,CDS_position=365,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=122,Codons=aCg/aGg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.365C>G,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	missense_variant	383	383	0.0	.	.	AC_Male=0;AF_NFE=9.10167e-06;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|2|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13213e-06;Hom=0;AF_POPMAX=9.10167e-06;AN_POPMAX=109870;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=9.15131e-06;GQ_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.57813e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.387e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.991),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=V/I,HGVSp=ENSP00000439263.1:p.Val125Ile,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=A:0,cDNA_position=383,CDS_position=373,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761622308,VARIANT_CLASS=SNV,Protein_position=125,Codons=Gtc/Atc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.373G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	missense_variant	390	390	0.0	.	.	AC_Male=5;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|5|2|2|3|0|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-65;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.79897e-05;Hom=0;AF_POPMAX=9.23483e-04;AN_POPMAX=15160;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|3|1|1|1|0|0|0|0|1|1|1|2|0|1|0|1|1|1;AF_Male=3.77729e-05;AF_AFR=9.23483e-04;AC_raw=15;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=8.25294e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36291e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=14;AC_AFR=14;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.06),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:0.0001096,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=G:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.994),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/R,HGVSp=ENSP00000439263.1:p.Lys127Arg,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0.0014,Allele=G,IMPACT=MODERATE,EXON=3/6,ExAC_AMR_MAF=G:0.001254,cDNA_position=390,CDS_position=380,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs144433221,VARIANT_CLASS=SNV,Protein_position=127,Codons=aAg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:1.071e-04,HGVSc=ENST00000543908.1:c.380A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	missense_variant	413	413	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|2|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16108e-109;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.24865e-05;Hom=0;AF_POPMAX=2.38223e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|3|0|0|0|0|0|1|1;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.25397e-01;Hom_EAS=0;AC_AMR=8;AF_ASJ=0.00000e+00;DP_MEDIAN=93;AF_Female=5.38812e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=6;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=8;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=2.38223e-04;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.09),UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:3.295e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,Feature_type=Transcript,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/S,HGVSp=ENSP00000439263.1:p.Pro135Ser,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=4/6,ExAC_AMR_MAF=T:0,cDNA_position=413,CDS_position=403,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs770678984,VARIANT_CLASS=SNV,Protein_position=135,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000543908.1:c.403C>T,ExAC_Adj_MAF=T:0.0003455
CDS|ENST00000543908	dbSNP	sequence_variant	1	1	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1345027263;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	5	5	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs892415557;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	6	6	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs774460908;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	8	8	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs748067291;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	10	10	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1346180677;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	15	15	0.0	+	.	consequence_type=missense_variant;id=rs771527303;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	17	17	0.0	+	.	consequence_type=missense_variant;id=rs772761859;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	18	18	0.0	+	.	consequence_type=missense_variant;id=rs1317068708;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	20	20	0.0	+	.	consequence_type=missense_variant;id=rs983223652;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	21	21	0.0	+	.	consequence_type=missense_variant;id=rs760309598;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	23	23	0.0	+	.	consequence_type=missense_variant;id=rs564172691;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	24	24	0.0	+	.	consequence_type=missense_variant;id=rs1314954450;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	25	25	0.0	+	.	consequence_type=synonymous_variant;id=rs1009445042;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	26	26	0.0	+	.	consequence_type=missense_variant;id=rs267604914;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	28	28	0.0	+	.	consequence_type=synonymous_variant;id=rs776210749;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	29	29	0.0	+	.	consequence_type=missense_variant;id=rs1292079143;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	30	30	0.0	+	.	consequence_type=missense_variant;id=rs1022554088;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	31	31	0.0	+	.	consequence_type=synonymous_variant;id=rs763334167;alleles=A%2CC%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	32	32	0.0	+	.	consequence_type=missense_variant;id=rs907713546;alleles=G%2CA%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	33	33	0.0	+	.	consequence_type=missense_variant;id=rs764406772;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	34	34	0.0	+	.	consequence_type=synonymous_variant;id=rs1253429311;alleles=A%2CC%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	35	35	0.0	+	.	consequence_type=missense_variant;id=rs752105945;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	40	40	0.0	+	.	consequence_type=synonymous_variant;id=rs757761311;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	41	41	0.0	+	.	consequence_type=missense_variant;id=rs767553043;alleles=C%2CA%2CG%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	42	42	0.0	+	.	consequence_type=missense_variant;id=rs750513385;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	43	43	0.0	+	.	consequence_type=synonymous_variant;id=rs1007666082;alleles=G%2CA%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	44	59	0.0	+	.	consequence_type=frameshift_variant;id=rs1306813664;alleles=CCGGCACCTCCGCTGC%2C-
CDS|ENST00000543908	dbSNP	sequence_variant	60	60	0.0	+	.	consequence_type=missense_variant;id=rs937347334;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	64	64	0.0	+	.	consequence_type=synonymous_variant;id=rs1229832497;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	66	66	0.0	+	.	consequence_type=missense_variant;id=rs1315229471;alleles=T%2CC%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	69	69	0.0	+	.	consequence_type=missense_variant;id=rs772952636;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	73	74	0.0	+	.	consequence_type=inframe_insertion;id=rs1219870401;alleles=-%2CGGGAAC
CDS|ENST00000543908	dbSNP	sequence_variant	80	80	0.0	+	.	consequence_type=missense_variant;id=rs746539074;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	81	81	0.0	+	.	consequence_type=missense_variant;id=rs1437942507;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	83	84	0.0	+	.	consequence_type=inframe_insertion;id=rs763191382;alleles=-%2CACGGCC
CDS|ENST00000543908	dbSNP	sequence_variant	86	86	0.0	+	.	consequence_type=missense_variant;id=rs770300796;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	87	87	0.0	+	.	consequence_type=missense_variant;id=rs1451260585;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	90	90	0.0	+	.	consequence_type=missense_variant;id=rs1362841019;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	91	91	0.0	+	.	consequence_type=missense_variant;id=rs776300314;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	92	92	0.0	+	.	consequence_type=missense_variant;id=rs1159616651;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	93	93	0.0	+	.	consequence_type=missense_variant;id=rs1185809906;alleles=A%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	97	97	0.0	+	.	consequence_type=missense_variant;id=rs759161485;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	99	99	0.0	+	.	consequence_type=missense_variant;id=rs764495116;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	101	101	0.0	+	.	consequence_type=missense_variant;id=rs774684452;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	104	104	0.0	+	.	consequence_type=missense_variant;id=rs976121906;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	108	108	0.0	+	.	consequence_type=missense_variant;id=rs895881728;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	109	109	0.0	+	.	consequence_type=missense_variant;id=rs762294220;alleles=C%2CG%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	112	112	0.0	+	.	consequence_type=synonymous_variant;id=rs768076232;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	121	121	0.0	+	.	consequence_type=synonymous_variant;id=rs1328029981;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	130	130	0.0	+	.	consequence_type=missense_variant;id=rs750844557;alleles=C%2CG%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	132	132	0.0	+	.	consequence_type=missense_variant;id=rs756247053;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	134	136	0.0	+	.	consequence_type=inframe_deletion;id=rs375981533;alleles=AAC%2C-
CDS|ENST00000543908	dbSNP	sequence_variant	138	138	0.0	+	.	consequence_type=missense_variant;id=rs1271597368;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	139	139	0.0	+	.	consequence_type=splice_region_variant;id=rs143955814;alleles=G%2CA%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	144	144	0.0	+	.	consequence_type=missense_variant;id=rs752810524;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	146	146	0.0	+	.	consequence_type=missense_variant;id=rs758247752;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	147	147	0.0	+	.	consequence_type=missense_variant;id=rs1199096532;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	150	150	0.0	+	.	consequence_type=missense_variant;id=rs1286861992;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	151	151	0.0	+	.	consequence_type=synonymous_variant;id=rs777402320;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	152	152	0.0	+	.	consequence_type=missense_variant;id=rs1192808116;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	153	153	0.0	+	.	consequence_type=missense_variant;id=rs1212522731;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	158	158	0.0	+	.	consequence_type=missense_variant;id=rs140455291;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	159	159	0.0	+	.	consequence_type=missense_variant;id=rs757177482;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	171	171	0.0	+	.	consequence_type=missense_variant;id=rs780748535;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	174	174	0.0	+	.	consequence_type=missense_variant;id=rs774451911;alleles=A%2CG%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	186	186	0.0	+	.	consequence_type=missense_variant;id=rs1468231466;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	191	191	0.0	+	.	consequence_type=missense_variant;id=rs3087878;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	196	196	0.0	+	.	consequence_type=synonymous_variant;id=rs375158125;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	201	201	0.0	+	.	consequence_type=missense_variant;id=rs201559014;alleles=A%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	203	203	0.0	+	.	consequence_type=missense_variant;id=rs779784731;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	211	211	0.0	+	.	consequence_type=synonymous_variant;id=rs141656657;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	213	213	0.0	+	.	consequence_type=missense_variant;id=rs1399730029;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	214	214	0.0	+	.	consequence_type=synonymous_variant;id=rs1315823029;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	220	220	0.0	+	.	consequence_type=synonymous_variant;id=rs369434915;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	230	230	0.0	+	.	consequence_type=missense_variant;id=rs1405046109;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	231	231	0.0	+	.	consequence_type=missense_variant;id=rs1284414737;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	232	232	0.0	+	.	consequence_type=synonymous_variant;id=rs184508172;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	235	235	0.0	+	.	consequence_type=missense_variant;id=rs1231776580;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	239	239	0.0	+	.	consequence_type=missense_variant;id=rs1281614790;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	245	245	0.0	+	.	consequence_type=missense_variant;id=rs761306458;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	251	251	0.0	+	.	consequence_type=start_lost;id=rs767459577;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	255	255	0.0	+	.	consequence_type=missense_variant;id=rs367954716;alleles=A%2CC%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	259	259	0.0	+	.	consequence_type=synonymous_variant;id=rs200633656;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	262	262	0.0	+	.	consequence_type=missense_variant;id=rs1018863986;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	271	271	0.0	+	.	consequence_type=missense_variant;id=rs1051019368;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	277	277	0.0	+	.	consequence_type=missense_variant;id=rs779405921;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	283	283	0.0	+	.	consequence_type=synonymous_variant;id=rs1382805858;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	296	296	0.0	+	.	consequence_type=missense_variant;id=rs1463089836;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	297	297	0.0	+	.	consequence_type=missense_variant;id=rs1308984921;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	298	298	0.0	+	.	consequence_type=synonymous_variant;id=rs372318247;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	304	304	0.0	+	.	consequence_type=synonymous_variant;id=rs754577624;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	310	310	0.0	+	.	consequence_type=synonymous_variant;id=rs1391388443;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	312	312	0.0	+	.	consequence_type=missense_variant;id=rs778561485;alleles=T%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	314	314	0.0	+	.	consequence_type=missense_variant;id=rs747390700;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	318	318	0.0	+	.	consequence_type=missense_variant;id=rs1335366133;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	319	319	0.0	+	.	consequence_type=missense_variant;id=rs771371139;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	320	320	0.0	+	.	consequence_type=missense_variant;id=rs563736659;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	322	322	0.0	+	.	consequence_type=synonymous_variant;id=rs746348189;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	323	323	0.0	+	.	consequence_type=missense_variant;id=rs1294041634;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	324	324	0.0	+	.	consequence_type=missense_variant;id=rs1416691571;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	326	326	0.0	+	.	consequence_type=missense_variant;id=rs868718436;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	328	328	0.0	+	.	consequence_type=synonymous_variant;id=rs1229714849;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	335	335	0.0	+	.	consequence_type=missense_variant;id=rs1348860194;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	336	336	0.0	+	.	consequence_type=missense_variant;id=rs770043528;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	342	342	0.0	+	.	consequence_type=missense_variant;id=rs775419569;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	343	343	0.0	+	.	consequence_type=synonymous_variant;id=rs972147914;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	344	344	0.0	+	.	consequence_type=missense_variant;id=rs1297768336;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	345	345	0.0	+	.	consequence_type=missense_variant;id=rs1443418786;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	346	346	0.0	+	.	consequence_type=synonymous_variant;id=rs1338651806;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	347	347	0.0	+	.	consequence_type=missense_variant;id=rs1196722115;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	349	349	0.0	+	.	consequence_type=synonymous_variant;id=rs1244710451;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	354	354	0.0	+	.	consequence_type=missense_variant;id=rs377156745;alleles=G%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	356	356	0.0	+	.	consequence_type=missense_variant;id=rs1182546534;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	363	363	0.0	+	.	consequence_type=missense_variant;id=rs1391284036;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	367	367	0.0	+	.	consequence_type=synonymous_variant;id=rs1253657974;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	375	375	0.0	+	.	consequence_type=missense_variant;id=rs764230766;alleles=C%2CG%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	376	376	0.0	+	.	consequence_type=synonymous_variant;id=rs1170526700;alleles=G%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	382	382	0.0	+	.	consequence_type=synonymous_variant;id=rs774578466;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	383	383	0.0	+	.	consequence_type=missense_variant;id=rs761622308;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	388	388	0.0	+	.	consequence_type=synonymous_variant;id=rs767261647;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	390	390	0.0	+	.	consequence_type=missense_variant;id=rs144433221;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	405	405	0.0	+	.	consequence_type=missense_variant;id=rs1377176181;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	413	413	0.0	+	.	consequence_type=missense_variant;id=rs770678984;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	419	419	0.0	+	.	consequence_type=missense_variant;id=rs927057705;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	431	431	0.0	+	.	consequence_type=synonymous_variant;id=rs151247418;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	446	446	0.0	+	.	consequence_type=synonymous_variant;id=rs776474941;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	449	449	0.0	+	.	consequence_type=synonymous_variant;id=rs1410437263;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	450	450	0.0	+	.	consequence_type=missense_variant;id=rs1283407561;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	461	461	0.0	+	.	consequence_type=synonymous_variant;id=rs759459614;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	470	470	0.0	+	.	consequence_type=synonymous_variant;id=rs372926712;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	472	472	0.0	+	.	consequence_type=missense_variant;id=rs775510228;alleles=C%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	473	473	0.0	+	.	consequence_type=synonymous_variant;id=rs146345914;alleles=G%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	474	474	0.0	+	.	consequence_type=missense_variant;id=rs1339503876;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	475	475	0.0	+	.	consequence_type=missense_variant;id=rs1445433341;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	476	476	0.0	+	.	consequence_type=missense_variant;id=rs866488889;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	477	477	0.0	+	.	consequence_type=missense_variant;id=rs1311826897;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	483	483	0.0	+	.	consequence_type=synonymous_variant;id=rs1259891285;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	495	495	0.0	+	.	consequence_type=missense_variant;id=rs764148755;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	496	496	0.0	+	.	consequence_type=missense_variant;id=rs150418753;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	503	503	0.0	+	.	consequence_type=synonymous_variant;id=rs757227703;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	504	504	0.0	+	.	consequence_type=missense_variant;id=rs781499966;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	509	509	0.0	+	.	consequence_type=missense_variant;id=rs746041079;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	510	510	0.0	+	.	consequence_type=missense_variant;id=rs756018179;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	512	512	0.0	+	.	consequence_type=synonymous_variant;id=rs369385342;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	514	514	0.0	+	.	consequence_type=missense_variant;id=rs779975972;alleles=C%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	530	530	0.0	+	.	consequence_type=synonymous_variant;id=rs768715452;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	540	540	0.0	+	.	consequence_type=missense_variant;id=rs774095582;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	542	542	0.0	+	.	consequence_type=synonymous_variant;id=rs199671891;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	548	548	0.0	+	.	consequence_type=synonymous_variant;id=rs112989351;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	549	549	0.0	+	.	consequence_type=missense_variant;id=rs1407256029;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	550	550	0.0	+	.	consequence_type=missense_variant;id=rs771441667;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	551	551	0.0	+	.	consequence_type=synonymous_variant;id=rs1330823537;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	554	554	0.0	+	.	consequence_type=synonymous_variant;id=rs1259991653;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	569	569	0.0	+	.	consequence_type=missense_variant;id=rs1303544092;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	570	570	0.0	+	.	consequence_type=missense_variant;id=rs919282095;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	572	572	0.0	+	.	consequence_type=synonymous_variant;id=rs772957252;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	578	578	0.0	+	.	consequence_type=missense_variant;id=rs375089291;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	581	581	0.0	+	.	consequence_type=synonymous_variant;id=rs770200317;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	592	592	0.0	+	.	consequence_type=missense_variant;id=rs775829411;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	598	598	0.0	+	.	consequence_type=missense_variant;id=rs763238851;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	599	599	0.0	+	.	consequence_type=synonymous_variant;id=rs1490869430;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	603	603	0.0	+	.	consequence_type=missense_variant;id=rs1342497115;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	604	604	0.0	+	.	consequence_type=missense_variant;id=rs764674925;alleles=C%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	605	605	0.0	+	.	consequence_type=splice_region_variant;id=rs752735481;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	613	613	0.0	+	.	consequence_type=missense_variant;id=rs758261924;alleles=A%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	615	615	0.0	+	.	consequence_type=missense_variant;id=rs777621617;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	629	629	0.0	+	.	consequence_type=synonymous_variant;id=rs1336872685;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	636	636	0.0	+	.	consequence_type=missense_variant;id=rs1331451303;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	651	651	0.0	+	.	consequence_type=synonymous_variant;id=rs1006739593;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	653	653	0.0	+	.	consequence_type=synonymous_variant;id=rs1264834130;alleles=G%2CA%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	655	655	0.0	+	.	consequence_type=missense_variant;id=rs746537411;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	659	659	0.0	+	.	consequence_type=synonymous_variant;id=rs770379933;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	665	665	0.0	+	.	consequence_type=synonymous_variant;id=rs780855060;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	671	671	0.0	+	.	consequence_type=synonymous_variant;id=rs1163522330;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	672	672	0.0	+	.	consequence_type=missense_variant;id=rs1429798567;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	689	689	0.0	+	.	consequence_type=synonymous_variant;id=rs146578323;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	695	695	0.0	+	.	consequence_type=synonymous_variant;id=rs970102977;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	710	710	0.0	+	.	consequence_type=synonymous_variant;id=rs201216212;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	711	711	0.0	+	.	consequence_type=missense_variant;id=rs1422769066;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	714	714	0.0	+	.	consequence_type=missense_variant;id=rs367724198;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	717	717	0.0	+	.	consequence_type=missense_variant;id=rs371122860;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	722	722	0.0	+	.	consequence_type=synonymous_variant;id=rs766086965;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	727	727	0.0	+	.	consequence_type=missense_variant;id=rs1196654054;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	729	729	0.0	+	.	consequence_type=missense_variant;id=rs772467109;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	738	738	0.0	+	.	consequence_type=missense_variant;id=rs1302511754;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	740	740	0.0	+	.	consequence_type=synonymous_variant;id=rs773804544;alleles=C%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	742	742	0.0	+	.	consequence_type=missense_variant;id=rs766531390;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	743	743	0.0	+	.	consequence_type=synonymous_variant;id=rs777042262;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	749	749	0.0	+	.	consequence_type=synonymous_variant;id=rs1266795902;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	750	750	0.0	+	.	consequence_type=missense_variant;id=rs759663986;alleles=C%2CA%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	752	752	0.0	+	.	consequence_type=synonymous_variant;id=rs765144876;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	755	755	0.0	+	.	consequence_type=synonymous_variant;id=rs1284923476;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	761	761	0.0	+	.	consequence_type=synonymous_variant;id=rs2239922;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	762	762	0.0	+	.	consequence_type=missense_variant;id=rs376218058;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	766	766	0.0	+	.	consequence_type=missense_variant;id=rs764042790;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	770	770	0.0	+	.	consequence_type=synonymous_variant;id=rs1486522613;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	782	782	0.0	+	.	consequence_type=splice_region_variant;id=rs1309883142;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	784	784	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs751459222;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	786	786	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs947563305;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	792	792	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs368198371;alleles=G%2CA%2CC%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	793	793	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs745596553;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	796	796	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs755720834;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	797	797	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs924255559;alleles=G%2CC%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	798	798	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs779694369;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	802	802	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs768855720;alleles=A%2C-
CDS|ENST00000543908	dbSNP	sequence_variant	803	803	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs748481474;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	809	809	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs772522385;alleles=C%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	810	810	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs372333025;alleles=G%2CA%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	814	814	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs771192956;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	815	815	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1398025727;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	820	820	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1220665736;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	821	821	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs776844227;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	823	823	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs759591941;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	837	837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1401133793;alleles=T%2C-
CDS|ENST00000543908	dbSNP	sequence_variant	837	837	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1409865549;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	843	843	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1170792757;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	854	854	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1477668015;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	861	861	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs536631976;alleles=G%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	873	873	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1157810473;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	875	875	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1261371990;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	879	879	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1216133569;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	883	883	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1447977408;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	884	884	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs943081202;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	888	888	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1394629576;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	894	894	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1054135007;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	898	898	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs892836444;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	916	916	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1284414785;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	924	924	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs558164797;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	925	925	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs996626589;alleles=T%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	931	931	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs997416578;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	940	940	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs570129756;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	941	943	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1047621162;alleles=GGC%2C-
CDS|ENST00000543908	dbSNP	sequence_variant	944	944	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1346546315;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	957	957	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs374957727;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	968	968	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1337790731;alleles=T%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	982	982	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs554173481;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	983	983	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs572559395;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	987	987	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1016477860;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	989	989	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1406820653;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	992	992	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs970132664;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	997	997	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1481486626;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	1003	1003	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1237212186;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	1011	1011	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1008089472;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	1020	1020	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1001619133;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	1029	1031	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1475877609;alleles=TGG%2C-
CDS|ENST00000543908	dbSNP	sequence_variant	1034	1034	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1015519281;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	1040	1040	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs961353095;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	1043	1043	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1267563319;alleles=A%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	1044	1044	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs960017469;alleles=C%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	1054	1054	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs542891999;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	1066	1066	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1026990450;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	45	45	0.0	+	.	consequence_type=missense_variant;id=rs756082410;alleles=C%2CA%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	46	46	0.0	+	.	consequence_type=synonymous_variant;id=rs780444510;alleles=G%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	47	47	0.0	+	.	consequence_type=missense_variant;id=rs1424340537;alleles=G%2CC
CDS|ENST00000543908	dbSNP	sequence_variant	48	48	0.0	+	.	consequence_type=missense_variant;id=rs973343235;alleles=C%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	50	50	0.0	+	.	consequence_type=missense_variant;id=rs754859910;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	51	51	0.0	+	.	consequence_type=missense_variant;id=rs1356403688;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	54	54	0.0	+	.	consequence_type=missense_variant;id=rs202061902;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	56	56	0.0	+	.	consequence_type=synonymous_variant;id=rs748150811;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	57	57	0.0	+	.	consequence_type=missense_variant;id=rs772038652;alleles=T%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	58	58	0.0	+	.	consequence_type=synonymous_variant;id=rs927228181;alleles=G%2CA
CDS|ENST00000543908	dbSNP	sequence_variant	132	134	0.0	+	.	consequence_type=inframe_deletion;id=rs766213031;alleles=ACA%2C-
CDS|ENST00000543908	dbSNP	sequence_variant	135	135	0.0	+	.	consequence_type=missense_variant;id=rs946116469;alleles=A%2CG
CDS|ENST00000543908	dbSNP	sequence_variant	136	136	0.0	+	.	consequence_type=synonymous_variant;id=rs766535198;alleles=C%2CT
CDS|ENST00000543908	dbSNP	sequence_variant	943	943	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1049559374;alleles=C%2CT
CDS|ENST00000543908	VCF	3_prime_UTR_variant	446	446	0.0	.	.	AC_Male=4;AF_NFE=5.37095e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-123;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43643e-05;Hom=0;AF_POPMAX=5.37095e-05;AN_POPMAX=111712;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|1;AF_Male=2.96512e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.30292e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=135;AF_Female=1.79598e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:4.942e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.991e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=4/6,ExAC_AMR_MAF=T:0,cDNA_position=446,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs776474941,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:4.942e-05,HGVSc=ENST00000543908.1:c.*22C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	449	449	0.0	.	.	AC_Male=0;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-101;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.05660e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=106;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12871e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=4/6,cDNA_position=449,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*25C>T
CDS|ENST00000543908	VCF	3_prime_UTR_variant	461	461	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-132;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.34426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=122;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.50786e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=4/6,ExAC_AMR_MAF=C:0,cDNA_position=461,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs759459614,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.*37T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	470	470	0.0	.	.	AC_Male=4;AF_NFE=1.16371e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|3|5|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-93;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=13;Hom_NFE=0;AF=5.27897e-05;Hom=0;AF_POPMAX=1.16371e-04;AN_POPMAX=111712;AC_NFE=13;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|2|1|1|0|0|1|0|0|1;AF_Male=2.96507e-05;AF_AFR=0.00000e+00;AC_raw=13;AB_MEDIAN=4.05405e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=97;AF_Female=8.08219e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|13;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.28067e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=13;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.27872e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:6.589e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001199,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=4/6,ExAC_AMR_MAF=A:0,cDNA_position=470,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs372926712,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:6.589e-05,HGVSc=ENST00000543908.1:c.*46C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	472	472	0.0	.	.	AC_Male=0;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-62;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=55;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99132e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=A,IMPACT=MODIFIER,EXON=4/6,ExAC_AMR_MAF=T:0,cDNA_position=472,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*48C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	472	472	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-188;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=145;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.99177e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=4/6,ExAC_AMR_MAF=T:0,cDNA_position=472,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*48C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	473	473	0.0	.	.	AC_Male=380;AF_NFE=2.32750e-03;Hom_FIN=3;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|2|40|88|203|202|119|49|4|0|0|0|0|0|0|0;AC_FIN=293;DREF_MEDIAN=5.01187e-117;AF_OTH=3.83072e-03;alleles=G%2CA;AF_FIN=1.31390e-02;AC_OTH=21;Hom_Male=2;AC=716;Hom_NFE=0;AF=2.90754e-03;Hom=4;AF_POPMAX=1.31390e-02;AN_POPMAX=22300;AC_NFE=260;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|5|6|15|17|25|30|39|50|52|47|44|38|56;AF_Male=2.81686e-03;AF_AFR=2.61370e-04;AC_raw=716;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=45;AF_ASJ=9.23858e-03;DP_MEDIAN=93;AF_Female=3.01740e-03;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|712;Hom_raw=4;AF_SAS=3.24865e-05;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=1;AC_Female=336;Hom_AFR=0;Hom_ASJ=1;AF_EAS=5.79777e-05;AC_SAS=1;POPMAX=FIN;AC_POPMAX=293;AC_AFR=4;Hom_SAS=0;AC_ASJ=91;AF_raw=2.90735e-03;Hom_Female=2;AF_AMR=1.34000e-03;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:0.002586,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0022,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0004,STRAND=1,ExAC_SAS_MAF=A:0.003311,EA_MAF=A:0.0005,Allele=A,IMPACT=MODIFIER,EXON=4/6,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=473,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000543908.1:c.*49G>A,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000543908	VCF	3_prime_UTR_variant	473	473	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-124;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.71429e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41835e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:0.002586,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0022,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0004,STRAND=1,ExAC_SAS_MAF=A:0.003311,EA_MAF=A:0.0005,Allele=T,IMPACT=MODIFIER,EXON=4/6,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=473,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000543908.1:c.*49G>T,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000543908	VCF	3_prime_UTR_variant	474	474	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-146;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.64198e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=162;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.16858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=4/6,cDNA_position=474,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*50G>A
CDS|ENST00000543908	VCF	3_prime_UTR_variant	475	475	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-92;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=74;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=4/6,cDNA_position=475,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*51A>C
CDS|ENST00000543908	VCF	3_prime_UTR_variant	495	495	0.0	.	.	AC_Male=0;AF_NFE=8.96282e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-295;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06345e-06;Hom=0;AF_POPMAX=8.96282e-06;AN_POPMAX=111572;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51327e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=226;AF_Female=8.98763e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.243e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=T:0,cDNA_position=495,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764148755,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*71C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	496	496	0.0	.	.	AC_Male=35;AF_NFE=1.07544e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|9|11|10|12|4|2|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-103;AF_OTH=1.82415e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=49;Hom_NFE=0;AF=1.99100e-04;Hom=0;AF_POPMAX=2.23441e-03;AN_POPMAX=9846;AC_NFE=12;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|4|3|1|2|1|6|7|4|4|0|2|1;AF_Male=2.59586e-04;AF_AFR=0.00000e+00;AC_raw=49;AB_MEDIAN=4.65116e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=2.23441e-03;DP_MEDIAN=74;AF_Female=1.25811e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|49;Hom_raw=0;AF_SAS=3.89838e-04;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=14;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=12;POPMAX=ASJ;AC_POPMAX=22;AC_AFR=0;Hom_SAS=0;AC_ASJ=22;AF_raw=1.98967e-04;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,PHENO=0&1,ExAC_EAS_MAF=A:0.0002225,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0002,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0002699,AFR_MAF=A:0.0005453,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=A:0,cDNA_position=496,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs150418753&COSM4067023,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:2.224e-04,HGVSc=ENST00000543908.1:c.*72G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	503	503	0.0	.	.	AC_Male=4;AF_NFE=5.37577e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00079e-202;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43754e-05;Hom=0;AF_POPMAX=5.37577e-05;AN_POPMAX=111612;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|1;AF_Male=2.96630e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=5.20944e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=152;AF_Female=1.79691e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35748e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,PHENO=0&1,ExAC_EAS_MAF=T:2.472e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=T:0,cDNA_position=503,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757227703&COSM4130155,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000543908.1:c.*79C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	504	504	0.0	.	.	AC_Male=5;AF_NFE=1.25390e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|2|3|9|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-94;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=17;Hom_NFE=0;AF=6.90524e-05;Hom=0;AF_POPMAX=1.25390e-04;AN_POPMAX=111652;AC_NFE=14;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|0|1|1|1|2|0|2|2|0|1|0|1|0|0;AF_Male=3.70749e-05;AF_AFR=0.00000e+00;AC_raw=17;AB_MEDIAN=5.09033e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=64;AF_Female=1.07790e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|17;Hom_raw=0;AF_SAS=9.74596e-05;AS_RF=9.36765e-01;Hom_AMR=0;AC_EAS=0;AC_Female=12;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=NFE;AC_POPMAX=14;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.90294e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:5.768e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:7.495e-05,AFR_MAF=A:0.0001211,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=A:0,cDNA_position=504,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs781499966,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:5.765e-05,HGVSc=ENST00000543908.1:c.*80G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	509	509	0.0	.	.	AC_Male=1;AF_NFE=3.58230e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-225;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62467e-05;Hom=0;AF_POPMAX=3.58230e-05;AN_POPMAX=111660;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.41499e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55048e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=196;AF_Female=2.69440e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:3.296e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:5.996e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=T:0,cDNA_position=509,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs746041079,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000543908.1:c.*85G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	510	510	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-212;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06141e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.11392e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=158;AF_Female=8.98134e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08869e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.239e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=G:0,cDNA_position=510,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756018179,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.*86C>G,ExAC_Adj_MAF=G:8.639e-05
CDS|ENST00000543908	VCF	3_prime_UTR_variant	514	514	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|1|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-130;AF_OTH=1.82282e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03062e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|1|1|0|0|0|0;AF_Male=1.48278e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=76;AF_Female=2.69426e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.39678e-01;Hom_AMR=0;AC_EAS=4;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,Allele=T,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=A:0&T:0,cDNA_position=514,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000543908.1:c.*90C>T,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	514	514	0.0	.	.	AC_Male=1;AF_NFE=8.95415e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-239;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21837e-05;Hom=0;AF_POPMAX=5.95557e-05;AN_POPMAX=33582;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.31915e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=153;AF_Female=1.79617e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.48089e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,Allele=A,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=A:0&T:0,cDNA_position=514,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000543908.1:c.*90C>A,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	530	530	0.0	.	.	AC_Male=1;AF_NFE=1.79045e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-65;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12163e-06;Hom=0;AF_POPMAX=1.79045e-05;AN_POPMAX=111704;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.08500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=57;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.42948e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=A:0,cDNA_position=530,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768715452,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.*106G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	540	540	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-238;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.42254e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=142;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.49406e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.499e-05,AFR_MAF=C:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=C:0,cDNA_position=540,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs774095582,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.*116G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	542	542	0.0	.	.	AC_Male=9;AF_NFE=2.32741e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|11|10|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-104;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=26;Hom_NFE=0;AF=1.05578e-04;Hom=0;AF_POPMAX=2.32741e-04;AN_POPMAX=111712;AC_NFE=26;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|3|0|2|5|0|2;AF_Male=6.67141e-05;AF_AFR=0.00000e+00;AC_raw=26;AB_MEDIAN=4.45780e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=98;AF_Female=1.52658e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|26;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=17;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=26;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.05574e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:9.885e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=T:0.0003,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001798,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=T:0,cDNA_position=542,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs199671891,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:9.884e-05,HGVSc=ENST00000543908.1:c.*118C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	549	549	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-102;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.59375e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=7.94592e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=5/6,cDNA_position=549,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*125C>T
CDS|ENST00000543908	VCF	3_prime_UTR_variant	550	550	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-67;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21820e-05;Hom=0;AF_POPMAX=1.01523e-04;AN_POPMAX=9850;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.62963e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=1.01523e-04;DP_MEDIAN=51;AF_Female=1.79601e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.498e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=A:0,cDNA_position=550,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs771441667,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.*126G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	551	551	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-154;AF_OTH=1.82282e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.60938e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=5/6,cDNA_position=551,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*127G>C
CDS|ENST00000543908	VCF	3_prime_UTR_variant	572	572	0.0	.	.	AC_Male=2;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21823e-05;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=1.48249e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.91803e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.01565e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:1.647e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=T:0,cDNA_position=572,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772957252,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000543908.1:c.*148C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	578	578	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-165;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95159e-06;AN_POPMAX=111712;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.56897e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=116;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17542e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=G:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=G:0,cDNA_position=578,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs375089291,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.*154C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	581	581	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-140;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.49153e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=118;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=G:0,cDNA_position=581,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs770200317,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.*157A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	592	592	0.0	.	.	AC_Male=1;AF_NFE=1.79054e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-248;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12196e-06;Hom=0;AF_POPMAX=1.79054e-05;AN_POPMAX=111698;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41312e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.99184e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=192;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.647e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=G:0,cDNA_position=592,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs775829411,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000543908.1:c.*168A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	598	598	0.0	.	.	AC_Male=0;AF_NFE=8.95399e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-226;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06124e-06;Hom=0;AF_POPMAX=8.95399e-06;AN_POPMAX=111682;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.30168e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=179;AF_Female=8.98150e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.22854e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=5/6,ExAC_AMR_MAF=G:0,cDNA_position=598,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763238851,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.*174A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	599	599	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-84;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06138e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.92754e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=69;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.86417e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=5/6,cDNA_position=599,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*175T>C
CDS|ENST00000543908	VCF	3_prime_UTR_variant	613	613	0.0	.	.	AC_Male=0;AF_NFE=8.97102e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-130;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06573e-06;Hom=0;AF_POPMAX=8.97102e-06;AN_POPMAX=111470;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.86905e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=168;AF_Female=8.98957e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.27e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=613,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs758261924,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*189A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	615	615	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|3|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-55;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62617e-05;Hom=0;AF_POPMAX=1.19133e-04;AN_POPMAX=33576;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48449e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.74078e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=1.79775e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.92315e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=1.19133e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.653e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=G:0,cDNA_position=615,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs777621617,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000543908.1:c.*191A>G,ExAC_Adj_MAF=G:0.0001728
CDS|ENST00000543908	VCF	3_prime_UTR_variant	653	653	0.0	.	.	AC_Male=1;AF_NFE=8.95367e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-83;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06121e-06;Hom=0;AF_POPMAX=8.95367e-06;AN_POPMAX=111686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41400e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.37037e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.49406e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=6/6,cDNA_position=653,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*229G>A
CDS|ENST00000543908	VCF	3_prime_UTR_variant	655	655	0.0	.	.	AC_Male=1;AF_NFE=8.95319e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-214;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12216e-06;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41334e-06;AF_AFR=6.53424e-05;AC_raw=2;AB_MEDIAN=4.72222e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=180;AF_Female=8.98085e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.48607e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:1.648e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=655,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746537411,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000543908.1:c.*231G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	659	659	0.0	.	.	AC_Male=2;AF_NFE=2.68562e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-156;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21825e-05;Hom=0;AF_POPMAX=2.68562e-05;AN_POPMAX=111706;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0;AF_Male=1.48265e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.28302e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33696e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=659,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs770379933,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*235C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	665	665	0.0	.	.	AC_Male=7;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|3|5|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-120;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.46675e-05;Hom=0;AF_POPMAX=3.24865e-04;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|2|1|2|0|0|0|0|1|1;AF_Male=5.18880e-05;AF_AFR=6.53424e-05;AC_raw=11;AB_MEDIAN=4.69613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=92;AF_Female=3.59202e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=3.24865e-04;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=10;POPMAX=SAS;AC_POPMAX=10;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:5.766e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0003634,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=665,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs780855060,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:5.765e-05,HGVSc=ENST00000543908.1:c.*241G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	672	672	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-66;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.42413e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=6/6,cDNA_position=672,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*248C>G
CDS|ENST00000543908	VCF	3_prime_UTR_variant	689	689	0.0	.	.	AC_Male=23;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|8|24|20|21|5|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.07688e-127;AF_OTH=1.82349e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=85;Hom_NFE=0;AF=3.45164e-04;Hom=1;AF_POPMAX=3.98589e-03;AN_POPMAX=15304;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|2|4|1|6|4|3|5|6|3|1|3|5;AF_Male=1.70492e-04;AF_AFR=3.98589e-03;AC_raw=85;AB_MEDIAN=4.72222e-01;Hom_EAS=0;AC_AMR=19;AF_ASJ=3.04569e-04;DP_MEDIAN=97;AF_Female=5.56773e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|84;Hom_raw=1;AF_SAS=3.24865e-05;AS_RF=9.53297e-01;Hom_AMR=0;AC_EAS=0;AC_Female=62;Hom_AFR=1;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=61;AC_AFR=61;Hom_SAS=0;AC_ASJ=3;AF_raw=3.45147e-04;Hom_Female=1;AF_AMR=5.65779e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:0.0004366,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0002,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0.0061,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0016,STRAND=1,ExAC_SAS_MAF=A:0.001101,EA_MAF=A:0.0052,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0.004228,cDNA_position=689,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs146578323,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:4.365e-04,HGVSc=ENST00000543908.1:c.*265G>A,ExAC_Adj_MAF=A:0.0005183
CDS|ENST00000543908	VCF	3_prime_UTR_variant	695	695	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-30;AF_OTH=1.82349e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=8.98037e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.72787e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=6/6,cDNA_position=695,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*271C>T
CDS|ENST00000543908	VCF	3_prime_UTR_variant	710	710	0.0	.	.	AC_Male=15;AF_NFE=3.58153e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|5|5|3|5|3|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-69;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=25;Hom_NFE=0;AF=1.01531e-04;Hom=0;AF_POPMAX=1.11082e-03;AN_POPMAX=15304;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|1|1|2|4|5|1|1|1|2|0|1|0;AF_Male=1.11200e-04;AF_AFR=1.11082e-03;AC_raw=25;AB_MEDIAN=4.82014e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98166e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|25;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.93009e-01;Hom_AMR=0;AC_EAS=0;AC_Female=10;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=17;AC_AFR=17;Hom_SAS=0;AC_ASJ=0;AF_raw=1.01514e-04;Hom_Female=0;AF_AMR=1.19111e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:4.943e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:2.997e-05,AFR_MAF=A:0,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0.0005,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0.0003844,cDNA_position=710,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs201216212,SAS_MAF=A:0.001,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:4.942e-05,HGVSc=ENST00000543908.1:c.*286G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	717	717	0.0	.	.	AC_Male=2;AF_NFE=1.79067e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|2|0|0|1|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=3.98107e-153;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=1.34541e-04;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03059e-05;Hom=0;AF_POPMAX=1.34541e-04;AN_POPMAX=22298;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;AF_Male=1.48262e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.69880e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=2.69450e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.45888e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:4.119e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=G:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=G:0,cDNA_position=717,ExAC_NFE_MAF=G:0.0004536,SYMBOL=NMT1,Existing_variation=rs371122860,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:4.118e-05,HGVSc=ENST00000543908.1:c.*293A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	722	722	0.0	.	.	AC_Male=1;AF_NFE=8.95383e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-154;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06128e-06;Hom=0;AF_POPMAX=8.95383e-06;AN_POPMAX=111684;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41345e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=115;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.499e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=722,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766086965,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*298C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	729	729	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-165;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06190e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.83051e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=118;AF_Female=8.98343e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53015e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.238e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=729,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772467109,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*305G>T,ExAC_Adj_MAF=T:8.64e-05
CDS|ENST00000543908	VCF	3_prime_UTR_variant	738	738	0.0	.	.	AC_Male=1;AF_NFE=8.96266e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-105;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06312e-06;Hom=0;AF_POPMAX=8.96266e-06;AN_POPMAX=111574;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41587e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.93750e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=64;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.78341e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=6/6,cDNA_position=738,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*314G>A
CDS|ENST00000543908	VCF	3_prime_UTR_variant	740	740	0.0	.	.	AC_Male=3;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|1|1|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-112;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43815e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|1|2|0|1;AF_Male=2.22499e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.63415e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=87;AF_Female=2.69648e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=4;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=1;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.24e-06&T:3.296e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05&T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0003467,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0&T:0,cDNA_position=740,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs773804544,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:8.236e-06&T:3.295e-05,HGVSc=ENST00000543908.1:c.*316C>T,ExAC_Adj_MAF=A:0&T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	740	740	0.0	.	.	AC_Male=1;AF_NFE=8.96379e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-101;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06359e-06;Hom=0;AF_POPMAX=8.96379e-06;AN_POPMAX=111560;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.41664e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.28571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=84;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.24e-06&T:3.296e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05&T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0003467,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0&T:0,cDNA_position=740,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs773804544,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:8.236e-06&T:3.295e-05,HGVSc=ENST00000543908.1:c.*316C>A,ExAC_Adj_MAF=A:0&T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	742	742	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=6.30957e-128;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=4.48471e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06345e-06;Hom=0;AF_POPMAX=4.48471e-05;AN_POPMAX=22298;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41642e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.81013e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=79;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54228e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.24e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0,cDNA_position=742,ExAC_NFE_MAF=A:0.0001512,SYMBOL=NMT1,Existing_variation=rs766531390,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.*318G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	743	743	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-131;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06342e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41675e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.35644e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=101;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.45417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.241e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=743,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs777042262,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*319G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	750	750	0.0	.	.	AC_Male=1;AF_NFE=1.79482e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-61;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21973e-05;Hom=0;AF_POPMAX=6.53424e-05;AN_POPMAX=15304;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|1|0|0|0|0|1|1|0|0|0|0;AF_Male=7.42027e-06;AF_AFR=6.53424e-05;AC_raw=4;AB_MEDIAN=4.60242e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.79872e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.84998e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.649e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.0001212,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=G:0,cDNA_position=750,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759663986,VARIANT_CLASS=SNV,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000543908.1:c.*326C>A,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	750	750	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-71;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21973e-05;Hom=0;AF_POPMAX=9.74659e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|1|1|0|0|0|0|0|0|0;AF_Male=2.22608e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.83333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=57;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=9.74659e-05;AS_RF=8.84998e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:1.649e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.0001212,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=G:0,cDNA_position=750,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759663986,VARIANT_CLASS=SNV,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000543908.1:c.*326C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	752	752	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|2|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38770e-91;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03277e-05;Hom=0;AF_POPMAX=2.89922e-04;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|1|0|1|1|1|0|0;AF_Male=2.22605e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=4.67647e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=1.79853e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43239e-01;Hom_AMR=0;AC_EAS=5;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.89922e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:3.298e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.0004622,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=G:0,cDNA_position=752,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs765144876,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:3.295e-05,HGVSc=ENST00000543908.1:c.*328A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	755	755	0.0	.	.	AC_Male=1;AF_NFE=8.97876e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-116;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06693e-06;Hom=0;AF_POPMAX=8.97876e-06;AN_POPMAX=111374;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.42269e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.18519e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=81;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.07420e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,PHENO=1,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,SOMATIC=1,Allele=G,IMPACT=MODIFIER,EXON=6/6,cDNA_position=755,SYMBOL=NMT1,Gene=ENSG00000136448,Existing_variation=COSM980092,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*331A>G
CDS|ENST00000543908	VCF	3_prime_UTR_variant	761	761	0.0	.	.	AC_Male=16886;AF_NFE=7.81798e-02;Hom_FIN=144;GQ_MEDIAN=99;AB_HIST_ALT=0|0|4|11|34|169|815|2369|5579|6526|6364|2859|1315|395|126|40|13|6|2|0;AC_FIN=2671;DREF_MEDIAN=1.58489e-82;AF_OTH=1.21898e-01;alleles=C%2CT;AF_FIN=1.19862e-01;AC_OTH=668;Hom_Male=1379;AC=32227;Hom_NFE=374;AF=1.31220e-01;Hom=2825;AF_POPMAX=2.70280e-01;AN_POPMAX=17234;AC_NFE=8690;AS_FilterStatus=PASS;Hom_OTH=38;DP_HIST_ALT=0|34|152|543|1210|1834|1980|1919|2086|2037|2144|2084|2059|2011|1891|1563|1322|1089|843|766;AF_Male=1.25481e-01;AF_AFR=1.64684e-01;AC_raw=32293;AB_MEDIAN=4.80000e-01;Hom_EAS=624;AC_AMR=8200;AF_ASJ=1.11156e-01;DP_MEDIAN=56;AF_Female=1.38175e-01;GQ_HIST_ALT=2|5|5|5|6|4|15|8|13|29|37|35|59|87|46|89|130|54|99|28732;Hom_raw=2833;AF_SAS=1.21133e-01;AS_RF=9.54732e-01;Hom_AMR=1132;AC_EAS=4658;AC_Female=15341;Hom_AFR=203;Hom_ASJ=67;AF_EAS=2.70280e-01;AC_SAS=3728;POPMAX=EAS;AC_POPMAX=4658;AC_AFR=2520;Hom_SAS=243;AC_ASJ=1092;AF_raw=1.31127e-01;Hom_Female=1446;AF_AMR=2.44470e-01;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,PHENO=0&1,ExAC_EAS_MAF=T:0.1255,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=T:0.084,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=T:0.1717,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.08058,AFR_MAF=T:0.1247,EAS_MAF=T:0.2003,EUR_MAF=T:0.2669,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.2664,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=T:0.1707,STRAND=1,ExAC_SAS_MAF=T:0.1082,EA_MAF=T:0.1609,SOMATIC=0&1,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0.1637,cDNA_position=761,ExAC_NFE_MAF=T:0.1181,SYMBOL=NMT1,Existing_variation=rs2239922&COSM4130156,SAS_MAF=T:0.0845,VARIANT_CLASS=SNV,AA_MAF=T:0.138,MINIMISED=1,ExAC_AFR_MAF=T:0.125,HGVSc=ENST00000543908.1:c.*337C>T,ExAC_Adj_MAF=T:0.2522
CDS|ENST00000543908	VCF	3_prime_UTR_variant	762	762	0.0	.	.	AC_Male=3;AF_NFE=2.70032e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|1|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-77;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.85053e-05;Hom=0;AF_POPMAX=1.96053e-04;AN_POPMAX=15302;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|1|0|1|0|1|0|1|1|1|1|0|0|0;AF_Male=2.22962e-05;AF_AFR=1.96053e-04;AC_raw=8;AB_MEDIAN=4.87441e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=3.60308e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51581e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=3;AC_AFR=3;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:3.303e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0.0002,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0.000289,cDNA_position=762,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs376218058,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000543908.1:c.*338G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	766	766	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-153;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07382e-06;Hom=0;AF_POPMAX=2.97992e-05;AN_POPMAX=33558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.13889e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=72;AF_Female=9.01015e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92885e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.264e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=766,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764042790,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000543908.1:c.*342G>T,ExAC_Adj_MAF=T:8.658e-05
CDS|ENST00000543908	VCF	3_prime_UTR_variant	770	770	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-66;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07485e-06;Hom=0;AF_POPMAX=3.24971e-05;AN_POPMAX=30772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43837e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24971e-05;AS_RF=9.36271e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=6/6,cDNA_position=770,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*346C>G
CDS|ENST00000543908	VCF	3_prime_UTR_variant	784	784	0.0	.	.	AC_Male=6;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|3|3|0|2|0|0|1|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.00371e-61;AF_OTH=1.82548e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=10;Hom_NFE=0;AF=4.08457e-05;Hom=0;AF_POPMAX=2.92664e-04;AN_POPMAX=30752;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|0|4|1|2|0|0|0|1|0|0|0|0|0;AF_Male=4.47227e-05;AF_AFR=0.00000e+00;AC_raw=10;AB_MEDIAN=5.13841e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=3.61454e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|10;Hom_raw=0;AF_SAS=2.92664e-04;AS_RF=9.37186e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=9;POPMAX=SAS;AC_POPMAX=9;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:3.322e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0.0002482,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0,cDNA_position=784,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs751459222,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000543908.1:c.*360G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	792	792	0.0	.	.	AC_Male=5;AF_NFE=2.72956e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|2|2|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-46;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.27643e-05;Hom=0;AF_POPMAX=1.62633e-04;AN_POPMAX=30744;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|3|1|0|2|0|0|0|0|0|0|0|0|0|0;AF_Male=3.73580e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.97648e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=2.71916e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=1.62633e-04;AS_RF=9.42843e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=5;POPMAX=SAS;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24852e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:3.333e-05&C:1.666e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=C:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05&C:1.512e-05,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&C:0,EA_MAF=C:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0&C:9.694e-05,cDNA_position=792,ExAC_NFE_MAF=A:0&C:0,SYMBOL=NMT1,Existing_variation=rs368198371,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:3.295e-05&C:1.647e-05,HGVSc=ENST00000543908.1:c.*368G>A,ExAC_Adj_MAF=A:0&C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	792	792	0.0	.	.	AC_Male=0;AF_NFE=9.09852e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-75;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.19108e-06;Hom=0;AF_POPMAX=6.53937e-05;AN_POPMAX=15292;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53937e-05;AC_raw=2;AB_MEDIAN=5.68093e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=50;AF_Female=1.81278e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:3.333e-05&C:1.666e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=C:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05&C:1.512e-05,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&C:0,EA_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0&C:9.694e-05,cDNA_position=792,ExAC_NFE_MAF=A:0&C:0,SYMBOL=NMT1,Existing_variation=rs368198371,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:3.295e-05&C:1.647e-05,HGVSc=ENST00000543908.1:c.*368G>C,ExAC_Adj_MAF=A:0&C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	792	792	0.0	.	.	AC_Male=1;AF_NFE=9.09852e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38634e-02;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09554e-06;Hom=0;AF_POPMAX=9.09852e-06;AN_POPMAX=109908;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.47161e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.78249e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=2.24518e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=3,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:3.333e-05&C:1.666e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=C:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05&C:1.512e-05,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&C:0,EA_MAF=C:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0&C:9.694e-05,cDNA_position=792,ExAC_NFE_MAF=A:0&C:0,SYMBOL=NMT1,Existing_variation=rs368198371,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:3.295e-05&C:1.647e-05,HGVSc=ENST00000543908.1:c.*368G>T,ExAC_Adj_MAF=A:0&C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	793	793	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-60;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09729e-06;Hom=0;AF_POPMAX=3.25309e-05;AN_POPMAX=30740;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.47496e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.31818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25309e-05;AS_RF=9.21292e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06065e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.335e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=G:0,cDNA_position=793,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs745596553,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000543908.1:c.*369T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	796	796	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-23;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10250e-06;Hom=0;AF_POPMAX=3.25436e-05;AN_POPMAX=30728;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48313e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.80952e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25436e-05;AS_RF=6.81301e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06068e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.343e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=C:0,cDNA_position=796,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs755720834,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.*372G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	797	797	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.92792e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06068e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=6/6,cDNA_position=797,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,HGVSc=ENST00000543908.1:c.*373G>T
CDS|ENST00000543908	VCF	3_prime_UTR_variant	797	797	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-75;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10667e-06;Hom=0;AF_POPMAX=2.98882e-05;AN_POPMAX=33458;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48929e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.94444e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.15833e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06068e-06;Hom_Female=0;AF_AMR=2.98882e-05;CSQ=ALLELE_NUM=2,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=6/6,cDNA_position=797,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,HGVSc=ENST00000543908.1:c.*373G>C
CDS|ENST00000543908	VCF	3_prime_UTR_variant	798	798	0.0	.	.	AC_Male=9;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|5|4|4|3|3|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.42191e-47;AF_OTH=1.46789e-03;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=8;Hom_Male=0;AC=23;Hom_NFE=0;AF=9.45693e-05;Hom=1;AF_POPMAX=4.48645e-04;AN_POPMAX=33434;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=1;DP_HIST_ALT=0|0|0|0|1|8|7|1|2|2|0|1|0|0|0|0|0|0|0|0;AF_Male=6.74987e-05;AF_AFR=0.00000e+00;AC_raw=23;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=15;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.27421e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|22;Hom_raw=1;AF_SAS=0.00000e+00;AS_RF=9.53311e-01;Hom_AMR=0;AC_EAS=0;AC_Female=14;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=15;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=9.33965e-05;Hom_Female=1;AF_AMR=4.48645e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:0.0001337,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:6.059e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0.001124,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0,cDNA_position=798,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs779694369,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:1.318e-04,HGVSc=ENST00000543908.1:c.*374C>A,ExAC_Adj_MAF=A:0.0009559
CDS|ENST00000543908	VCF	3_prime_UTR_variant	801	802	0.0	.	.	AC_Male=1;AF_NFE=9.18341e-06;Hom_FIN=0;GQ_MEDIAN=50;AB_HIST_ALT=0|1|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.93432e-01;AF_OTH=0.00000e+00;alleles=CA%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12347e-06;Hom=0;AF_POPMAX=9.18341e-06;AN_POPMAX=108892;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.51948e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.73810e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=0.00000e+00;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=2.94458e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12143e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=-:8.371e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=-:1.517e-05,AFR_MAF=-:0,Feature_type=Transcript,HGVS_OFFSET=4,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=-:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=-:0,Allele=-,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=-:0,cDNA_position=802,ExAC_NFE_MAF=-:0,SYMBOL=NMT1,Existing_variation=rs768855720,VARIANT_CLASS=deletion,MINIMISED=1,ExAC_AFR_MAF=-:8.237e-06,HGVSc=ENST00000543908.1:c.*382delA,ExAC_Adj_MAF=-:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	803	803	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-60;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.23547e-05;Hom=0;AF_POPMAX=1.74034e-04;AN_POPMAX=17238;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=1.50204e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=6.03448e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=9.11826e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.32362e-01;Hom_AMR=0;AC_EAS=3;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.74034e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21821e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:2.511e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.00035,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=G:0,cDNA_position=803,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs748481474,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:2.471e-05,HGVSc=ENST00000543908.1:c.*379A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	809	809	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=44;AB_HIST_ALT=0|0|2|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98091e-05;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15076e-06;Hom=0;AF_POPMAX=2.99778e-05;AN_POPMAX=33358;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.36364e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.19439e-06;GQ_HIST_ALT=0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.32543e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21822e-05;Hom_Female=0;AF_AMR=2.99778e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:1.681e-05,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.041e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=809,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772522385,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000543908.1:c.*385C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	810	810	0.0	.	.	AC_Male=35;AF_NFE=4.44502e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|5|11|9|15|15|6|4|1|1|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-56;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=65;Hom_NFE=0;AF=2.69557e-04;Hom=0;AF_POPMAX=6.38866e-04;AN_POPMAX=17218;AC_NFE=48;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|2|2|7|7|4|10|10|7|9|3|2|1|1|1|1|0|0|0|0;AF_Male=2.64602e-04;AF_AFR=1.31234e-04;AC_raw=67;AB_MEDIAN=5.11628e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=1.05263e-04;DP_MEDIAN=35;AF_Female=2.75578e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|1|65;Hom_raw=0;AF_SAS=6.59065e-05;AS_RF=9.51341e-01;Hom_AMR=0;AC_EAS=11;AC_Female=30;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.38866e-04;AC_SAS=2;POPMAX=EAS;AC_POPMAX=11;AC_AFR=2;Hom_SAS=0;AC_ASJ=1;AF_raw=2.72068e-04;Hom_Female=0;AF_AMR=2.99383e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:0.0002436&C:8.401e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0007,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0003347&C:1.521e-05,EAS_MAF=A:0,EUR_MAF=A:0.001,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0005856&C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0&C:0,EA_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:9.743e-05&C:0,cDNA_position=810,ExAC_NFE_MAF=A:0&C:0,SYMBOL=NMT1,Existing_variation=rs372333025,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:2.471e-04&C:1.647e-05,HGVSc=ENST00000543908.1:c.*386G>A,ExAC_Adj_MAF=A:0&C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	810	810	0.0	.	.	AC_Male=0;AF_NFE=9.26046e-06;Hom_FIN=0;GQ_MEDIAN=58;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.78115e-03;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.14704e-06;Hom=0;AF_POPMAX=9.26046e-06;AN_POPMAX=107986;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.95455e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.18594e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.25955e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12143e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:0.0002436&C:8.401e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=A:0.0007,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0003347&C:1.521e-05,EAS_MAF=A:0,EUR_MAF=A:0.001,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0005856&C:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0&C:0,EA_MAF=A:0,Allele=C,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:9.743e-05&C:0,cDNA_position=810,ExAC_NFE_MAF=A:0&C:0,SYMBOL=NMT1,Existing_variation=rs372333025,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:2.471e-04&C:1.647e-05,HGVSc=ENST00000543908.1:c.*386G>C,ExAC_Adj_MAF=A:0&C:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	814	814	0.0	.	.	AC_Male=0;AF_NFE=9.31845e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38634e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.17188e-06;Hom=0;AF_POPMAX=9.31845e-06;AN_POPMAX=107314;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.28161e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.24334e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.21785e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12163e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.418e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.523e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0,cDNA_position=814,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs771192956,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000543908.1:c.*390G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	815	815	0.0	.	.	AC_Male=0;AF_NFE=9.31463e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-39;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.17091e-06;Hom=0;AF_POPMAX=9.31463e-06;AN_POPMAX=107358;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.11765e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=9.23890e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99330e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06081e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=3_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=6/6,cDNA_position=815,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.*391T>C
CDS|ENST00000543908	VCF	3_prime_UTR_variant	821	821	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-80;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.22258e-06;Hom=0;AF_POPMAX=1.10473e-04;AN_POPMAX=9052;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.70167e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.12698e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.10473e-04;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52221e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06105e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=T:8.481e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.531e-05,AFR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=T:0,cDNA_position=821,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs776844227,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000543908.1:c.*397C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000543908	VCF	3_prime_UTR_variant	823	823	0.0	.	.	AC_Male=1;AF_NFE=9.48047e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-30;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.23858e-06;Hom=0;AF_POPMAX=9.48047e-06;AN_POPMAX=105480;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.73013e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.16667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.85059e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06114e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.491e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.532e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/6,ExAC_AMR_MAF=A:0,cDNA_position=823,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs759591941,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000543908.1:c.*399G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	inframe_deletion	131	134	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-19;AF_OTH=0.00000e+00;alleles=TACA%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63922e-05;Hom=0;AF_POPMAX=2.63817e-04;AN_POPMAX=15162;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24225e-05;AF_AFR=2.63817e-04;AC_raw=4;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07243e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.21158e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=4;AC_AFR=4;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=-:3.614e-05,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=-:0,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=-:0,AFR_MAF=-:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=2,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=-:0,ENSP=ENSP00000439263,Consequence=inframe_deletion&NMD_transcript_variant,Amino_acids=YN/Y,HGVSp=ENSP00000439263.1:p.Asn42del,STRAND=1,ExAC_SAS_MAF=-:0,EA_MAF=-:0.0007,Allele=-,IMPACT=MODERATE,EXON=1/6,ExAC_AMR_MAF=-:0.0004244,cDNA_position=132-134,CDS_position=122-124,ExAC_NFE_MAF=-:0,SYMBOL=NMT1,Existing_variation=rs766213031,VARIANT_CLASS=deletion,Protein_position=41-42,Codons=tACAac/tac,MINIMISED=1,ExAC_AFR_MAF=-:3.295e-05,HGVSc=ENST00000543908.1:c.124_126delAAC,ExAC_Adj_MAF=-:0
CDS|ENST00000543908	VCF	splice_region_variant	139	139	0.0	.	.	AC_Male=4;AF_NFE=2.73010e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25597e-29;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.64955e-05;Hom=0;AF_POPMAX=6.65513e-05;AN_POPMAX=15026;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=3.00680e-05;AF_AFR=6.65513e-05;AC_raw=4;AB_MEDIAN=5.27778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.27137e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62425e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:9.22e-06,TREMBL=Q9Y465&B7Z8J4,ExAC_MAF=C:0.0001,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.668e-05,AFR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=splice_region_variant&synonymous_variant&NMD_transcript_variant,Amino_acids=R,HGVSp=ENST00000543908.1:c.129G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=C:0,Allele=A,IMPACT=LOW,EXON=1/6,ExAC_AMR_MAF=A:0,cDNA_position=139,CDS_position=129,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs143955814,VARIANT_CLASS=SNV,Protein_position=43,Codons=cgG/cgA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.129G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	splice_region_variant	604	604	0.0	.	.	AC_Male=0;AF_NFE=8.95592e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06167e-06;Hom=0;AF_POPMAX=8.95592e-06;AN_POPMAX=111658;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=8.98198e-06;GQ_HIST_ALT=0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.79803e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=A:8.237e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000439263,Consequence=splice_region_variant&3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=5/6,ExAC_AMR_MAF=A:0,cDNA_position=604,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764674925,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000543908.1:c.*180C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000543908	VCF	splice_region_variant	605	605	0.0	.	.	AC_Male=0;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=0.00000e+00;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07040e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.75083e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=301;AF_Female=9.00009e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.23711e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.3e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.507e-05,AFR_MAF=C:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=splice_region_variant&3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=LOW,EXON=6/6,ExAC_AMR_MAF=C:0,cDNA_position=605,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs752735481,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000543908.1:c.*181A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000543908	VCF	5_prime_UTR_variant	1	1	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-28;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10971e-06;Hom=0;AF_POPMAX=3.26456e-05;AN_POPMAX=30632;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49221e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.26316e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.26456e-05;AS_RF=8.77261e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=5_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=1/6,cDNA_position=1,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.-10G>C
CDS|ENST00000543908	VCF	5_prime_UTR_variant	6	6	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-38;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09396e-06;Hom=0;AF_POPMAX=3.25797e-05;AN_POPMAX=30694;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46425e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25797e-05;AS_RF=8.95290e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=G:8.698e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000439263,Consequence=5_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=1/6,ExAC_AMR_MAF=G:0,cDNA_position=6,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774460908,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000543908.1:c.-5T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000543908	VCF	5_prime_UTR_variant	8	8	0.0	.	.	AC_Male=0;AF_NFE=9.03653e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-42;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.18371e-06;Hom=0;AF_POPMAX=3.00282e-05;AN_POPMAX=33302;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.85556e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.81238e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.38885e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=3.00282e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI00019150A9,ExAC_EAS_MAF=C:8.678e-06,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000439263,Consequence=5_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=1/6,ExAC_AMR_MAF=C:0,cDNA_position=8,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs748067291,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000543908.1:c.-3A>C,ExAC_Adj_MAF=C:8.983e-05
CDS|ENST00000543908	VCF	5_prime_UTR_variant	10	10	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=13;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.77267e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.86832e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000439263,UNIPARC=UPI00019150A9,Consequence=5_prime_UTR_variant&NMD_transcript_variant,TREMBL=Q9Y465&B7Z8J4,Feature=ENST00000543908,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=1/6,cDNA_position=10,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000543908.1:c.-1G>A
CDS|ENST00000585561	VCF	coding_sequence_variant	1	1	0.0	.	.	AC_Male=0;AF_NFE=9.04748e-06;Hom_FIN=0;GQ_MEDIAN=20;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.90099e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.19363e-06;Hom=0;AF_POPMAX=3.00571e-05;AN_POPMAX=33270;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.81594e-05;GQ_HIST_ALT=0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.32038e-03;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=3.00571e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.651e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=coding_sequence_variant&NMD_transcript_variant,Amino_acids=X,HGVSp=ENST00000585561.1:c.1C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=1,CDS_position=2,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs771527303,VARIANT_CLASS=SNV,Protein_position=1,Codons=nCg/nTg,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000585561.1:c.1C>T,ExAC_Adj_MAF=T:8.965e-05
CDS|ENST00000585561	VCF	inframe_insertion	59	59	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-72;AF_OTH=1.82548e-04;alleles=A%2CAGGGAAC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07030e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42611e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.09091e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.02292e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=14,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=inframe_insertion&NMD_transcript_variant,Amino_acids=-/GN,HGVSp=ENSP00000466777.1:p.Asn24_Gly25dup,STRAND=1,Allele=GGGAAC,IMPACT=MODERATE,EXON=1/7,cDNA_position=59-60,CDS_position=60-61,SYMBOL=NMT1,VARIANT_CLASS=insertion,Protein_position=20-21,Codons=-/GGGAAC,MINIMISED=1,HGVSc=ENST00000585561.1:c.68_73dupGAACGG
CDS|ENST00000585561	VCF	inframe_insertion	69	69	0.0	.	.	AC_Male=5;AF_NFE=5.38871e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|2|2|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=5.01187e-60;AF_OTH=0.00000e+00;alleles=A%2CAACGGCC;AF_FIN=4.48994e-05;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84877e-05;Hom=0;AF_POPMAX=5.38871e-05;AN_POPMAX=111344;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|2|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=3.71261e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=3.80952e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80109e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.11301e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84241e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=ACGGCC:2.556e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=ACGGCC:4.635e-05,AFR_MAF=ACGGCC:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=ACGGCC:0,ENSP=ENSP00000466777,Consequence=inframe_insertion&NMD_transcript_variant,Amino_acids=N/NGH,HGVSp=ENSP00000466777.1:p.Gly25_His26dup,STRAND=1,ExAC_SAS_MAF=ACGGCC:0,Allele=ACGGCC,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=ACGGCC:0,cDNA_position=69-70,CDS_position=70-71,ExAC_NFE_MAF=ACGGCC:0,SYMBOL=NMT1,Existing_variation=rs763191382,VARIANT_CLASS=insertion,Protein_position=24,Codons=aac/aACGGCCac,MINIMISED=1,ExAC_AFR_MAF=ACGGCC:2.471e-05,HGVSc=ENST00000585561.1:c.71_76dupCGGCCA,ExAC_Adj_MAF=ACGGCC:0
CDS|ENST00000585561	VCF	synonymous_variant	14	14	0.0	.	.	AC_Male=3;AF_NFE=3.60536e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|3|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00010e-44;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44872e-05;Hom=0;AF_POPMAX=5.96516e-05;AN_POPMAX=33528;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|1|0|2|1|0|0|0|1|0|0|0|0|0|0;AF_Male=2.23125e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.54132e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=2.71316e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43635e-05;Hom_Female=0;AF_AMR=5.96516e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:3.427e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:6.219e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000585561.1:c.14G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=14,CDS_position=15,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs776210749,VARIANT_CLASS=SNV,Protein_position=5,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:3.295e-05,HGVSc=ENST00000585561.1:c.14G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	synonymous_variant	20	20	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16473e-06;Hom=0;AF_POPMAX=6.50407e-05;AN_POPMAX=30750;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43837e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=6.00160e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50407e-05;AS_RF=9.41280e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=A,HGVSp=ENST00000585561.1:c.20A>G(p.%253D),STRAND=1,Allele=G,IMPACT=LOW,EXON=1/7,cDNA_position=20,CDS_position=21,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=7,Codons=gcA/gcG,HGVSc=ENST00000585561.1:c.20A>G
CDS|ENST00000585561	VCF	synonymous_variant	20	20	0.0	.	.	AC_Male=0;AF_NFE=9.01534e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-23;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08237e-06;Hom=0;AF_POPMAX=9.01534e-06;AN_POPMAX=110922;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.04830e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.51046e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=A,HGVSp=ENST00000585561.1:c.20A>C(p.%253D),STRAND=1,Allele=C,IMPACT=LOW,EXON=1/7,cDNA_position=20,CDS_position=21,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=7,Codons=gcA/gcC,HGVSc=ENST00000585561.1:c.20A>C
CDS|ENST00000585561	VCF	synonymous_variant	26	26	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-133;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08523e-06;Hom=0;AF_POPMAX=3.25373e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.44225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.78313e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=83;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25373e-05;AS_RF=8.78960e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.561e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=K,HGVSp=ENST00000585561.1:c.26G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=26,CDS_position=27,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs757761311,VARIANT_CLASS=SNV,Protein_position=9,Codons=aaG/aaA,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000585561.1:c.26G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	synonymous_variant	32	32	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-56;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16067e-06;Hom=0;AF_POPMAX=6.50745e-05;AN_POPMAX=30734;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48723e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.23810e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.50745e-05;AS_RF=8.94107e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.542e-06&C:8.542e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0&C:1.55e-05,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&C:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=P,HGVSp=ENST00000585561.1:c.32G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&C:0,Allele=T,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=T:0&C:0,cDNA_position=32,CDS_position=33,ExAC_NFE_MAF=T:0&C:0,SYMBOL=NMT1,Existing_variation=rs780444510,VARIANT_CLASS=SNV,Protein_position=11,Codons=ccG/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06&C:8.237e-06,HGVSc=ENST00000585561.1:c.32G>T,ExAC_Adj_MAF=T:0&C:0
CDS|ENST00000585561	VCF	synonymous_variant	42	42	0.0	.	.	AC_Male=1;AF_NFE=2.69721e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-37;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22188e-05;Hom=0;AF_POPMAX=2.69721e-05;AN_POPMAX=111226;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.42843e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.80333e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97663e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.515e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.545e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=L,HGVSp=ENST00000585561.1:c.42C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=42,CDS_position=43,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs748150811,VARIANT_CLASS=SNV,Protein_position=15,Codons=Ctg/Ttg,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.42C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	synonymous_variant	50	50	0.0	.	.	AC_Male=0;AF_NFE=8.98828e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-59;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07106e-06;Hom=0;AF_POPMAX=8.98828e-06;AN_POPMAX=111256;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.77273e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00982e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05614e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=Q,HGVSp=ENST00000585561.1:c.50G>A(p.%253D),STRAND=1,Allele=A,IMPACT=LOW,EXON=1/7,cDNA_position=50,CDS_position=51,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=17,Codons=caG/caA,MINIMISED=1,HGVSc=ENST00000585561.1:c.50G>A
CDS|ENST00000585561	VCF	synonymous_variant	95	95	0.0	.	.	AC_Male=0;AF_NFE=9.00236e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.84034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07857e-06;Hom=0;AF_POPMAX=9.00236e-06;AN_POPMAX=111082;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.63736e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=13;AF_Female=9.02543e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.58906e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.666e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.57e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=C,HGVSp=ENST00000585561.1:c.95C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=95,CDS_position=96,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs762294220,VARIANT_CLASS=SNV,Protein_position=32,Codons=tgC/tgT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.95C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	synonymous_variant	98	98	0.0	.	.	AC_Male=0;AF_NFE=1.80050e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-23;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15614e-06;Hom=0;AF_POPMAX=1.80050e-05;AN_POPMAX=111080;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.76923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=19;AF_Female=1.80473e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.41561e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:1.741e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:3.152e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000585561.1:c.98G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=98,CDS_position=99,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768076232,VARIANT_CLASS=SNV,Protein_position=33,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000585561.1:c.98G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	synonymous_variant	107	107	0.0	.	.	AC_Male=0;AF_NFE=9.01567e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.22517e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08407e-06;Hom=0;AF_POPMAX=9.01567e-06;AN_POPMAX=110918;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.97806e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.57456e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000585561.1:c.107G>A(p.%253D),STRAND=1,Allele=A,IMPACT=LOW,EXON=1/7,cDNA_position=107,CDS_position=108,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=36,Codons=gaG/gaA,MINIMISED=1,HGVSc=ENST00000585561.1:c.107G>A
CDS|ENST00000585561	VCF	synonymous_variant	116	116	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-88;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=1.02270e-04;AN_POPMAX=9778;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.40984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=1.02270e-04;DP_MEDIAN=61;AF_Female=9.06914e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.25490e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:9.018e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=S,HGVSp=ENST00000585561.1:c.116C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,Allele=T,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=116,CDS_position=117,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=39,Codons=agC/agT,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.116C>T,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	synonymous_variant	122	122	0.0	.	.	AC_Male=9;AF_NFE=7.26388e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|1|0|3|1|2|2|4|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-29;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.75899e-05;Hom=0;AF_POPMAX=9.84252e-05;AN_POPMAX=30480;AC_NFE=8;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|3|2|2|6|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=6.75017e-05;AF_AFR=0.00000e+00;AC_raw=15;AB_MEDIAN=4.19355e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=4.55506e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|13;Hom_raw=0;AF_SAS=9.84252e-05;AS_RF=9.10989e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=9.08540e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:0.0001008,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001161,AFR_MAF=T:0.0001995,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=N,HGVSp=ENST00000585561.1:c.122C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=122,CDS_position=123,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs766535198,VARIANT_CLASS=SNV,Protein_position=41,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:9.060e-05,HGVSc=ENST00000585561.1:c.122C>T,ExAC_Adj_MAF=T:9.878e-05
CDS|ENST00000585561	VCF	synonymous_variant	137	137	0.0	.	.	AC_Male=148;AF_NFE=1.34979e-03;Hom_FIN=0;GQ_MEDIAN=80;AB_HIST_ALT=0|0|4|13|34|85|90|44|24|6|1|2|0|0|1|0|0|0|0|0;AC_FIN=74;DREF_MEDIAN=1.00000e-08;AF_OTH=1.30939e-03;alleles=T%2CC;AF_FIN=3.42910e-03;AC_OTH=7;Hom_Male=0;AC=275;Hom_NFE=0;AF=1.14690e-03;Hom=0;AF_POPMAX=3.42910e-03;AN_POPMAX=21580;AC_NFE=145;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|5|4|20|31|38|39|37|27|29|22|24|7|6|3|2|2|0|1;AF_Male=1.12191e-03;AF_AFR=1.81476e-03;AC_raw=304;AB_MEDIAN=3.07692e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=1.23127e-03;DP_MEDIAN=42;AF_Female=1.17747e-03;GQ_HIST_ALT=4|4|6|8|5|9|8|12|6|14|13|6|13|13|19|10|18|17|12|107;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=5.26862e-02;Hom_AMR=0;AC_EAS=6;AC_Female=127;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.51206e-04;AC_SAS=0;POPMAX=FIN;AC_POPMAX=74;AC_AFR=27;Hom_SAS=0;AC_ASJ=12;AF_raw=1.24619e-03;Hom_Female=0;AF_AMR=1.20409e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:0.001857,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0.001923,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0.001052,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=S,HGVSp=ENST00000585561.1:c.137T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0.005814,Allele=C,IMPACT=LOW,EXON=2/7,ExAC_AMR_MAF=C:0.001447,cDNA_position=137,CDS_position=138,ExAC_NFE_MAF=C:0.01002,SYMBOL=NMT1,Existing_variation=rs777402320,VARIANT_CLASS=SNV,Protein_position=46,Codons=agT/agC,MINIMISED=1,ExAC_AFR_MAF=C:1.911e-03,HGVSc=ENST00000585561.1:c.137T>C,ExAC_Adj_MAF=C:0.000438
CDS|ENST00000585561	VCF	synonymous_variant	197	197	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|1|2|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.10793e-31;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.78394e-05;Hom=0;AF_POPMAX=3.99467e-04;AN_POPMAX=15020;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|1|2|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.68939e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.91379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=4.11794e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.74988e-01;Hom_AMR=0;AC_EAS=6;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.99467e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.46164e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:6.366e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=G:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_start_NF,EAS_MAF=G:0,EUR_MAF=G:0.003,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.001103,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,GMAF=G:0.0006,Amino_acids=K,HGVSp=ENST00000585561.1:c.197A>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=LOW,EXON=2/7,ExAC_AMR_MAF=G:0,cDNA_position=197,CDS_position=198,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs141656657,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=66,AA_MAF=G:0,Codons=aaA/aaG,MINIMISED=1,ExAC_AFR_MAF=G:3.314e-05,HGVSc=ENST00000585561.1:c.197A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	synonymous_variant	200	200	0.0	.	.	AC_Male=0;AF_NFE=1.12471e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.76844e-06;Hom=0;AF_POPMAX=1.12471e-05;AN_POPMAX=88912;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.05753e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.93464e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10344e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=G,HGVSp=ENST00000585561.1:c.200C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=2/7,cDNA_position=200,CDS_position=201,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=67,Codons=ggC/ggT,MINIMISED=1,HGVSc=ENST00000585561.1:c.200C>T
CDS|ENST00000585561	VCF	synonymous_variant	206	206	0.0	.	.	AC_Male=6;AF_NFE=8.41548e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|2|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15518e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=3.50814e-05;Hom=0;AF_POPMAX=8.41548e-05;AN_POPMAX=83180;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|1|0|2|1|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=5.48296e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.21637e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.10980e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12023e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.28394e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:5.723e-05,ExAC_MAF=A:0.0001,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001152,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=E,HGVSp=ENST00000585561.1:c.206G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0,Allele=A,IMPACT=LOW,EXON=2/7,ExAC_AMR_MAF=A:0,cDNA_position=206,CDS_position=207,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs369434915,VARIANT_CLASS=SNV,Protein_position=69,Codons=gaG/gaA,MINIMISED=1,ExAC_AFR_MAF=A:2.496e-05,HGVSc=ENST00000585561.1:c.206G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	synonymous_variant	218	218	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-83;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.48408e-06;Hom=0;AF_POPMAX=9.03506e-05;AN_POPMAX=11068;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=9.03506e-05;AC_raw=1;AB_MEDIAN=6.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.21150e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.96517e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:2.3e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=T:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,GMAF=T:0.0002,Amino_acids=A,HGVSp=ENST00000585561.1:c.218C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=2/7,ExAC_AMR_MAF=T:0.0002112,cDNA_position=218,CDS_position=219,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs184508172,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=73,AA_MAF=T:0,Codons=gcC/gcT,MINIMISED=1,ExAC_AFR_MAF=T:8.398e-06,HGVSc=ENST00000585561.1:c.218C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	synonymous_variant	254	254	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=20;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.42787e-06;AF_OTH=.;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=.;DP_MEDIAN=3;AF_Female=0.00000e+00;GQ_HIST_ALT=0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=1;AF_SAS=.;AS_RF=8.77050e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=.;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.31752e-04;Hom_Female=0;AF_AMR=.;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=synonymous_variant&NMD_transcript_variant,Amino_acids=Y,HGVSp=ENST00000585561.1:c.254C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/7,cDNA_position=254,CDS_position=255,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=85,Codons=taC/taT,MINIMISED=1,HGVSc=ENST00000585561.1:c.254C>T
CDS|ENST00000585561	VCF	missense_variant	3	3	0.0	.	.	AC_Male=1;AF_NFE=9.02755e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-30;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.17307e-06;Hom=0;AF_POPMAX=6.58762e-05;AN_POPMAX=15180;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44923e-06;AF_AFR=6.58762e-05;AC_raw=2;AB_MEDIAN=4.35484e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=9.05272e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.20566e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.622e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.564e-05,AFR_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.882),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=D/H,HGVSp=ENSP00000466777.1:p.Asp2His,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=C:0,cDNA_position=3,CDS_position=4,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs772761859,VARIANT_CLASS=SNV,Protein_position=2,Codons=Gac/Cac,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000585561.1:c.3G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	missense_variant	6	6	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16887e-06;Hom=0;AF_POPMAX=6.51339e-05;AN_POPMAX=30706;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=1.80973e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.51339e-05;AS_RF=9.34226e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.458),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=E/K,HGVSp=ENSP00000466777.1:p.Glu3Lys,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=1/7,cDNA_position=6,CDS_position=7,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=3,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000585561.1:c.6G>A
CDS|ENST00000585561	VCF	missense_variant	7	7	0.0	.	.	AC_Male=0;AF_NFE=9.01990e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08360e-06;Hom=0;AF_POPMAX=9.01990e-06;AN_POPMAX=110866;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=9.04732e-06;GQ_HIST_ALT=0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17447e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.595e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.559e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.359),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=E/G,HGVSp=ENSP00000466777.1:p.Glu3Gly,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=7,CDS_position=8,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs760309598,VARIANT_CLASS=SNV,Protein_position=3,Codons=gAg/gGg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000585561.1:c.7A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	9	9	0.0	.	.	AC_Male=31;AF_NFE=9.01518e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|4|2|10|15|9|8|6|1|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.15479e-38;AF_OTH=3.66838e-04;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=56;Hom_NFE=0;AF=2.28573e-04;Hom=0;AF_POPMAX=3.07603e-03;AN_POPMAX=17230;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|3|15|10|7|8|3|3|1|4|1|1|0|0|0|0|0|0;AF_Male=2.30614e-04;AF_AFR=0.00000e+00;AC_raw=56;AB_MEDIAN=4.76557e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=2.26093e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|56;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.34281e-01;Hom_AMR=0;AC_EAS=53;AC_Female=25;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.07603e-03;AC_SAS=0;POPMAX=EAS;AC_POPMAX=53;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.27391e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:0.0002232,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,FLAGS=cds_start_NF,EAS_MAF=C:0,EUR_MAF=C:0.001,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.773),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0.002947,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,GMAF=C:0.0002,Amino_acids=S/R,HGVSp=ENSP00000466777.1:p.Ser4Arg,STRAND=1,ExAC_SAS_MAF=C:0.001171,Allele=C,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=C:0,cDNA_position=9,CDS_position=10,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs564172691,SAS_MAF=C:0,VARIANT_CLASS=SNV,Protein_position=4,AA_MAF=C:0,Codons=Agt/Cgt,MINIMISED=1,ExAC_AFR_MAF=C:2.142e-04,HGVSc=ENST00000585561.1:c.9A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	missense_variant	10	10	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08090e-06;Hom=0;AF_POPMAX=3.25330e-05;AN_POPMAX=30738;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43760e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25330e-05;AS_RF=8.76833e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.07),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.517),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/N,HGVSp=ENSP00000466777.1:p.Ser4Asn,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=1/7,cDNA_position=10,CDS_position=11,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=4,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000585561.1:c.10G>A
CDS|ENST00000585561	VCF	missense_variant	15	15	0.0	.	.	AC_Male=0;AF_NFE=9.01372e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-34;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08110e-06;Hom=0;AF_POPMAX=9.01372e-06;AN_POPMAX=110942;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.80000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.04454e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.06165e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.714),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=T/P,HGVSp=ENSP00000466777.1:p.Thr6Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/7,cDNA_position=15,CDS_position=16,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=6,Codons=Aca/Cca,MINIMISED=1,HGVSc=ENST00000585561.1:c.15A>C
CDS|ENST00000585561	VCF	missense_variant	18	18	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52365e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/T,HGVSp=ENSP00000466777.1:p.Ala7Thr,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=1/7,cDNA_position=18,CDS_position=19,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=7,Codons=Gca/Aca,HGVSc=ENST00000585561.1:c.18G>A
CDS|ENST00000585561	VCF	missense_variant	18	18	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-45;AF_OTH=1.83756e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08320e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.55556e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.05108e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.37319e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.999),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/P,HGVSp=ENSP00000466777.1:p.Ala7Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/7,cDNA_position=18,CDS_position=19,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=7,Codons=Gca/Cca,HGVSc=ENST00000585561.1:c.18G>C
CDS|ENST00000585561	VCF	missense_variant	19	19	0.0	.	.	AC_Male=4;AF_NFE=9.02104e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|2|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-43;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63397e-05;Hom=0;AF_POPMAX=9.75864e-05;AN_POPMAX=30742;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=2.97699e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.70769e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=9.75864e-05;AS_RF=9.42769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=SAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.713e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.554e-05,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.997),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/V,HGVSp=ENSP00000466777.1:p.Ala7Val,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=19,CDS_position=20,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764406772,VARIANT_CLASS=SNV,Protein_position=7,Codons=gCa/gTa,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.19C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	missense_variant	21	21	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-39;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08257e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=26;AF_Female=9.04846e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.15769e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.19),UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.556e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.059),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=V/L,HGVSp=ENSP00000466777.1:p.Val8Leu,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=C:0,cDNA_position=21,CDS_position=22,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs752105945,VARIANT_CLASS=SNV,Protein_position=8,Codons=Gtg/Ctg,MINIMISED=1,ExAC_AFR_MAF=C:8.237e-06,HGVSc=ENST00000585561.1:c.21G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	missense_variant	27	27	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=11;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.87339e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.42),UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.554e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.007),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/S,HGVSp=ENSP00000466777.1:p.Pro10Ser,STRAND=1,ExAC_SAS_MAF=A:0,Allele=T,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=27,CDS_position=28,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=10,Codons=Ccg/Tcg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000585561.1:c.27C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	missense_variant	27	27	0.0	.	.	AC_Male=0;AF_NFE=9.02006e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38634e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08397e-06;Hom=0;AF_POPMAX=9.02006e-06;AN_POPMAX=110864;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.70833e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=18;AF_Female=9.05403e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.26525e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=tolerated_low_confidence(0.17),UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.554e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.553e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.116),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/T,HGVSp=ENSP00000466777.1:p.Pro10Thr,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=27,CDS_position=28,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs767553043,VARIANT_CLASS=SNV,Protein_position=10,Codons=Ccg/Acg,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000585561.1:c.27C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	missense_variant	28	28	0.0	.	.	AC_Male=2;AF_NFE=9.01664e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-48;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.16573e-06;Hom=0;AF_POPMAX=3.25267e-05;AN_POPMAX=30744;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.48792e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63469e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=3.25267e-05;AS_RF=9.40560e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.16),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.71e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.552e-05,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/L,HGVSp=ENSP00000466777.1:p.Pro10Leu,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=28,CDS_position=29,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs750513385,VARIANT_CLASS=SNV,Protein_position=10,Codons=cCg/cTg,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.28C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	missense_variant	31	31	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=62;AB_HIST_ALT=0|0|2|0|0|2|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25280e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22474e-05;Hom=0;AF_POPMAX=6.50703e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|1|0|2|0|1|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.44025e-06;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=21;AF_Female=1.80920e-05;GQ_HIST_ALT=1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.50703e-05;AS_RF=1.16160e-02;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=2.98401e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.6),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.71e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.017),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/L,HGVSp=ENSP00000466777.1:p.Pro11Leu,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=31,CDS_position=32,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=11,Codons=cCg/cTg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.31C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	missense_variant	31	31	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=58;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.80083e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08247e-06;Hom=0;AF_POPMAX=3.25351e-05;AN_POPMAX=30736;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.95563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=53;AF_Female=9.04601e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25351e-05;AS_RF=1.45870e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.71e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.000124,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.935),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/Q,HGVSp=ENSP00000466777.1:p.Pro11Gln,STRAND=1,ExAC_SAS_MAF=T:0,Allele=A,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=31,CDS_position=32,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs756082410,VARIANT_CLASS=SNV,Protein_position=11,Codons=cCg/cAg,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.31C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	missense_variant	33	33	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-63;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08007e-06;Hom=0;AF_POPMAX=5.80181e-05;AN_POPMAX=17236;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60976e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=41;AF_Female=9.04094e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96821e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.12),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.009),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/P,HGVSp=ENSP00000466777.1:p.Ala12Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/7,cDNA_position=33,CDS_position=34,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=12,Codons=Gca/Cca,MINIMISED=1,HGVSc=ENST00000585561.1:c.33G>C
CDS|ENST00000585561	VCF	missense_variant	36	36	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97164e-32;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15627e-06;Hom=0;AF_POPMAX=1.16063e-04;AN_POPMAX=17232;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.57018e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=1.80682e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.52227e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.16063e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.11),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.534e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.046),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001174,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/S,HGVSp=ENSP00000466777.1:p.Pro13Ser,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=T:0,cDNA_position=36,CDS_position=37,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754859910,VARIANT_CLASS=SNV,Protein_position=13,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000585561.1:c.36C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	missense_variant	37	37	0.0	.	.	AC_Male=1;AF_NFE=2.69964e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.37387e-64;AF_OTH=1.83217e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63090e-05;Hom=0;AF_POPMAX=2.69964e-05;AN_POPMAX=111126;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.03446e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=2.70929e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36654e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.647),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/L,HGVSp=ENSP00000466777.1:p.Pro13Leu,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=1/7,cDNA_position=37,CDS_position=38,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=13,Codons=cCt/cTt,MINIMISED=1,HGVSc=ENST00000585561.1:c.37C>T
CDS|ENST00000585561	VCF	missense_variant	40	40	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-53;AF_OTH=1.83083e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22264e-05;Hom=0;AF_POPMAX=6.58068e-05;AN_POPMAX=15196;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43262e-06;AF_AFR=6.58068e-05;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=1.80460e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35197e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80181e-05;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.705e-05,ExAC_MAF=T:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,EAS_MAF=T:0.0014,EUR_MAF=T:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.084),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,GMAF=T:0.0002,Amino_acids=P/L,HGVSp=ENSP00000466777.1:p.Pro14Leu,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=T:0.0001013,cDNA_position=40,CDS_position=41,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs202061902,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=14,AA_MAF=T:0,Codons=cCg/cTg,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.40C>T,ExAC_Adj_MAF=T:8.969e-05
CDS|ENST00000585561	VCF	missense_variant	43	43	0.0	.	.	AC_Male=1;AF_NFE=8.98893e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-25;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07236e-06;Hom=0;AF_POPMAX=8.98893e-06;AN_POPMAX=111248;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42765e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.62500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.85),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:1.703e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.089e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=L/R,HGVSp=ENSP00000466777.1:p.Leu15Arg,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=43,CDS_position=44,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772038652,VARIANT_CLASS=SNV,Protein_position=15,Codons=cTg/cGg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000585561.1:c.43T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	52	52	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-33;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14120e-06;Hom=0;AF_POPMAX=5.96019e-05;AN_POPMAX=33556;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42589e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.78231e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=5.96019e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=M/R,HGVSp=ENSP00000466777.1:p.Met18Arg,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=1/7,cDNA_position=52,CDS_position=53,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=18,Codons=aTg/aGg,HGVSc=ENST00000585561.1:c.52T>G
CDS|ENST00000585561	VCF	missense_variant	52	52	0.0	.	.	AC_Male=0;AF_NFE=8.98650e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-65;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07060e-06;Hom=0;AF_POPMAX=8.98650e-06;AN_POPMAX=111278;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=9.00901e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43341e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.058),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=M/T,HGVSp=ENSP00000466777.1:p.Met18Thr,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/7,cDNA_position=52,CDS_position=53,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=18,Codons=aTg/aCg,HGVSc=ENST00000585561.1:c.52T>C
CDS|ENST00000585561	VCF	missense_variant	55	55	0.0	.	.	AC_Male=7;AF_NFE=9.88373e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|3|1|3|3|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-45;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=11;Hom_NFE=0;AF=4.47784e-05;Hom=0;AF_POPMAX=9.88373e-05;AN_POPMAX=111294;AC_NFE=11;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|1|4|0|1|0|2|0|1|0|1|0|0|0|0;AF_Male=5.19889e-05;AF_AFR=0.00000e+00;AC_raw=11;AB_MEDIAN=4.18860e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.60328e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|11;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53117e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=11;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.46661e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:7.653e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0.0001388,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.361),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=M/R,HGVSp=ENSP00000466777.1:p.Met19Arg,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=55,CDS_position=56,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs772952636,VARIANT_CLASS=SNV,Protein_position=19,Codons=aTg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:7.413e-05,HGVSc=ENST00000585561.1:c.55T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	66	66	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=52;AB_HIST_ALT=0|0|1|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.20127e-01;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07090e-06;Hom=0;AF_POPMAX=2.98098e-05;AN_POPMAX=33546;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.16667e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=9.00836e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.23972e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=2.98098e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.52e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.905),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/R,HGVSp=ENSP00000466777.1:p.Gly23Arg,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=66,CDS_position=67,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs746539074,VARIANT_CLASS=SNV,Protein_position=23,Codons=Ggg/Agg,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000585561.1:c.66G>A,ExAC_Adj_MAF=A:9.027e-05
CDS|ENST00000585561	VCF	missense_variant	67	67	0.0	.	.	AC_Male=1;AF_NFE=8.98182e-06;Hom_FIN=0;GQ_MEDIAN=54;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=4.54545e-02;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98182e-06;AN_POPMAX=111336;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42688e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.26923e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.37827e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.1),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.721),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/A,HGVSp=ENSP00000466777.1:p.Gly23Ala,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/7,cDNA_position=67,CDS_position=68,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=23,Codons=gGg/gCg,MINIMISED=1,HGVSc=ENST00000585561.1:c.67G>C
CDS|ENST00000585561	VCF	missense_variant	72	72	0.0	.	.	AC_Male=0;AF_NFE=8.98230e-06;Hom_FIN=0;GQ_MEDIAN=57;AB_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.53267e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07070e-06;Hom=0;AF_POPMAX=8.98230e-06;AN_POPMAX=111330;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.38095e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=9.00722e-06;GQ_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.31156e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.43),UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.529e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.546e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.03),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/S,HGVSp=ENSP00000466777.1:p.Gly25Ser,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=72,CDS_position=73,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs770300796,VARIANT_CLASS=SNV,Protein_position=25,Codons=Ggc/Agc,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000585561.1:c.72G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	missense_variant	77	77	0.0	.	.	AC_Male=1;AF_NFE=8.98101e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-38;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07024e-06;Hom=0;AF_POPMAX=8.98101e-06;AN_POPMAX=111346;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42721e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.37664e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.539e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.547e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.898),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=H/Q,HGVSp=ENSP00000466777.1:p.His26Gln,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=77,CDS_position=78,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs776300314,VARIANT_CLASS=SNV,Protein_position=26,Codons=caT/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000585561.1:c.77T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	79	79	0.0	.	.	AC_Male=0;AF_NFE=8.98505e-06;Hom_FIN=0;GQ_MEDIAN=53;AB_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=8.31688e-02;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07130e-06;Hom=0;AF_POPMAX=8.98505e-06;AN_POPMAX=111296;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=2.51984e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=25;AF_Female=9.00690e-06;GQ_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.21757e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,PHENO=1,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.649),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=E/V,HGVSp=ENSP00000466777.1:p.Glu27Val,STRAND=1,SOMATIC=1,Allele=T,IMPACT=MODERATE,EXON=1/7,cDNA_position=79,CDS_position=80,SYMBOL=NMT1,Existing_variation=COSM1128678,VARIANT_CLASS=SNV,Protein_position=27,Codons=gAg/gTg,MINIMISED=1,HGVSc=ENST00000585561.1:c.79A>T
CDS|ENST00000585561	VCF	missense_variant	83	83	0.0	.	.	AC_Male=0;AF_NFE=8.98957e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-73;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07286e-06;Hom=0;AF_POPMAX=8.98957e-06;AN_POPMAX=111240;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.37037e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=54;AF_Female=9.01128e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.05502e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.571e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.553e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.996),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=H/Q,HGVSp=ENSP00000466777.1:p.His28Gln,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=83,CDS_position=84,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs759161485,VARIANT_CLASS=SNV,Protein_position=28,Codons=caC/caG,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000585561.1:c.83C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	85	85	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-32;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07425e-06;Hom=0;AF_POPMAX=5.80518e-05;AN_POPMAX=17226;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43362e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.34667e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.80518e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.588e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.998),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001181,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=C/Y,HGVSp=ENSP00000466777.1:p.Cys29Tyr,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=85,CDS_position=86,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764495116,VARIANT_CLASS=SNV,Protein_position=29,Codons=tGc/tAc,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000585561.1:c.85G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	missense_variant	87	87	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-26;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22221e-05;Hom=0;AF_POPMAX=8.96111e-05;AN_POPMAX=33478;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43329e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.21053e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.80297e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.53191e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=8.96111e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:1.721e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.488),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/G,HGVSp=ENSP00000466777.1:p.Ser30Gly,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=87,CDS_position=88,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs774684452,VARIANT_CLASS=SNV,Protein_position=30,Codons=Agc/Ggc,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000585561.1:c.87A>G,ExAC_Adj_MAF=G:0.0001836
CDS|ENST00000585561	VCF	missense_variant	116	116	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-29;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09614e-06;Hom=0;AF_POPMAX=3.26861e-05;AN_POPMAX=30594;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.47005e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.26861e-05;AS_RF=8.82577e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:9.018e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.647),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/R,HGVSp=ENSP00000466777.1:p.Ser39Arg,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=116,CDS_position=117,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs750844557,VARIANT_CLASS=SNV,Protein_position=39,Codons=agC/agG,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.116C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	118	118	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92478e-20;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.09799e-06;Hom=0;AF_POPMAX=5.83158e-05;AN_POPMAX=17148;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.91667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07293e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.95804e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.83158e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.03),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:9.058e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.006),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.0001227,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Y/C,HGVSp=ENSP00000466777.1:p.Tyr40Cys,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=G:0,cDNA_position=118,CDS_position=119,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756247053,VARIANT_CLASS=SNV,Protein_position=40,Codons=tAc/tGc,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000585561.1:c.118A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	121	121	0.0	.	.	AC_Male=1;AF_NFE=9.07738e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-55;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.11265e-06;Hom=0;AF_POPMAX=9.07738e-06;AN_POPMAX=110164;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49805e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.29412e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.17479e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06068e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.37),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.007),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=N/S,HGVSp=ENSP00000466777.1:p.Asn41Ser,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=1/7,cDNA_position=121,CDS_position=122,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=41,Codons=aAc/aGc,MINIMISED=1,HGVSc=ENST00000585561.1:c.121A>G
CDS|ENST00000585561	VCF	missense_variant	124	124	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=7;AB_HIST_ALT=0|0|2|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.66338e-01;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=4.53227e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12712e-06;Hom=0;AF_POPMAX=4.53227e-05;AN_POPMAX=22064;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.52298e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=0.00000e+00;GQ_HIST_ALT=1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.73728e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21819e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.919),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=R/P,HGVSp=ENSP00000466777.1:p.Arg42Pro,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=1/7,cDNA_position=124,CDS_position=125,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=42,Codons=cGg/cCg,MINIMISED=1,HGVSc=ENST00000585561.1:c.124G>C
CDS|ENST00000585561	VCF	missense_variant	132	132	0.0	.	.	AC_Male=1;AF_NFE=9.20793e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-78;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13846e-06;Hom=0;AF_POPMAX=9.20793e-06;AN_POPMAX=108602;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.53477e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=50;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.26429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09934e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.03),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.304e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.508e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.341),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=L/V,HGVSp=ENSP00000466777.1:p.Leu45Val,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=G:0,cDNA_position=132,CDS_position=133,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs758247752,VARIANT_CLASS=SNV,Protein_position=45,Codons=Ttg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000585561.1:c.132T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	133	133	0.0	.	.	AC_Male=1;AF_NFE=9.20082e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-91;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13363e-06;Hom=0;AF_POPMAX=9.20082e-06;AN_POPMAX=108686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.52627e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.83900e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.982),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=L/W,HGVSp=ENSP00000466777.1:p.Leu45Trp,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=2/7,cDNA_position=133,CDS_position=134,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=45,Codons=tTg/tGg,MINIMISED=1,HGVSc=ENST00000585561.1:c.133T>G
CDS|ENST00000585561	VCF	missense_variant	136	136	0.0	.	.	AC_Male=1;AF_NFE=9.18628e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-41;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12361e-06;Hom=0;AF_POPMAX=9.18628e-06;AN_POPMAX=108858;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.50875e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.88840e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09927e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.027),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=S/N,HGVSp=ENSP00000466777.1:p.Ser46Asn,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=2/7,cDNA_position=136,CDS_position=137,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=46,Codons=aGt/aAt,MINIMISED=1,HGVSc=ENST00000585561.1:c.136G>A
CDS|ENST00000585561	VCF	missense_variant	138	138	0.0	.	.	AC_Male=0;AF_NFE=9.18577e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-80;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12368e-06;Hom=0;AF_POPMAX=9.18577e-06;AN_POPMAX=108864;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=9.14645e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40367e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.04),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.562),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=P/A,HGVSp=ENSP00000466777.1:p.Pro47Ala,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=2/7,cDNA_position=138,CDS_position=139,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=47,Codons=Cca/Gca,MINIMISED=1,HGVSc=ENST00000585561.1:c.138C>G
CDS|ENST00000585561	VCF	missense_variant	144	144	0.0	.	.	AC_Male=6;AF_NFE=4.58573e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|3|2|4|8|1|1|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-54;AF_OTH=1.83352e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=21;Hom_NFE=0;AF=8.63501e-05;Hom=0;AF_POPMAX=9.81804e-04;AN_POPMAX=15278;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|2|5|2|2|2|0|3|0|0|1|0|1|0|0|1;AF_Male=4.49384e-05;AF_AFR=9.81804e-04;AC_raw=21;AB_MEDIAN=5.21739e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=1.36761e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|21;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=15;AC_AFR=15;Hom_SAS=0;AC_ASJ=0;AF_raw=8.60860e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.37),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.336e-05,ExAC_MAF=G:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=G:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.034e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,EAS_MAF=G:0,EUR_MAF=G:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.009),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,GMAF=G:0.0002,Amino_acids=N/D,HGVSp=ENSP00000466777.1:p.Asn49Asp,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0.0011,Allele=G,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=G:0.000789,cDNA_position=144,CDS_position=145,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs140455291,SAS_MAF=G:0,VARIANT_CLASS=SNV,Protein_position=49,AA_MAF=G:0,Codons=Aat/Gat,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-05,HGVSc=ENST00000585561.1:c.144A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	145	145	0.0	.	.	AC_Male=2;AF_NFE=5.50327e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.29463e-76;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.46765e-05;Hom=0;AF_POPMAX=5.50327e-05;AN_POPMAX=109026;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AF_Male=1.49817e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.64551e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=3.64797e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53507e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.45964e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:2.508e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:4.569e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.016),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=N/S,HGVSp=ENSP00000466777.1:p.Asn49Ser,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=G:0,cDNA_position=145,CDS_position=146,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs757177482,VARIANT_CLASS=SNV,Protein_position=49,Codons=aAt/aGt,MINIMISED=1,ExAC_AFR_MAF=G:2.471e-05,HGVSc=ENST00000585561.1:c.145A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	157	157	0.0	.	.	AC_Male=3;AF_NFE=4.59441e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|2|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-54;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.05744e-05;Hom=0;AF_POPMAX=4.59441e-05;AN_POPMAX=108828;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|2|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24908e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.80645e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.82428e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99531e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.04965e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.12),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:4.372e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.027e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.011),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/V,HGVSp=ENSP00000466777.1:p.Ala53Val,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=T:0,cDNA_position=157,CDS_position=158,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs780748535,VARIANT_CLASS=SNV,Protein_position=53,Codons=gCc/gTc,MINIMISED=1,ExAC_AFR_MAF=T:4.118e-05,HGVSc=ENST00000585561.1:c.157C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	missense_variant	160	160	0.0	.	.	AC_Male=6;AF_NFE=6.46365e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|1|0|3|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-50;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.88843e-05;Hom=0;AF_POPMAX=6.46365e-05;AN_POPMAX=108298;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|2|1|1|0|0|0|0|0|1|0|0|0|0;AF_Male=4.50857e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.32432e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=9.15198e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.86984e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.306),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/R,HGVSp=ENSP00000466777.1:p.Lys54Arg,STRAND=1,ExAC_SAS_MAF=T:0&G:0,Allele=G,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=T:0&G:0,cDNA_position=160,CDS_position=161,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=54,Codons=aAa/aGa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000585561.1:c.160A>G,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000585561	VCF	missense_variant	160	160	0.0	.	.	AC_Male=1;AF_NFE=9.23378e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-64;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12633e-06;Hom=0;AF_POPMAX=9.23378e-06;AN_POPMAX=108298;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.51428e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.22727e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09977e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=possibly_damaging(0.748),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/I,HGVSp=ENSP00000466777.1:p.Lys54Ile,STRAND=1,ExAC_SAS_MAF=T:0&G:0,Allele=T,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=T:0&G:0,cDNA_position=160,CDS_position=161,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,Protein_position=54,Codons=aAa/aTa,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000585561.1:c.160A>T,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000585561	VCF	missense_variant	172	172	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-24;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15155e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.12500e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=9.21302e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=2.89217e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10004e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.12),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=benign(0.016),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/R,HGVSp=ENSP00000466777.1:p.Lys58Arg,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=2/7,cDNA_position=172,CDS_position=173,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=58,Codons=aAg/aGg,MINIMISED=1,HGVSc=ENST00000585561.1:c.172A>G
CDS|ENST00000585561	VCF	missense_variant	189	189	0.0	.	.	AC_Male=0;AF_NFE=9.88807e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-130;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.33099e-06;Hom=0;AF_POPMAX=9.88807e-06;AN_POPMAX=101132;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.14563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=9.61908e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33183e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10129e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:1.315e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.529e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Low_complexity_(Seg):seg,PolyPhen=probably_damaging(0.994),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=K/E,HGVSp=ENSP00000466777.1:p.Lys64Glu,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=G:0,cDNA_position=189,CDS_position=190,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779784731,VARIANT_CLASS=SNV,Protein_position=64,Codons=Aaa/Gaa,MINIMISED=1,ExAC_AFR_MAF=G:8.261e-06,HGVSc=ENST00000585561.1:c.189A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	missense_variant	199	199	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30719e-25;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.87099e-05;Hom=0;AF_POPMAX=1.31596e-04;AN_POPMAX=30396;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.55437e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.49730e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.03795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66438e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64119e-05;Hom_Female=0;AF_AMR=1.31596e-04;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.564),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=G/V,HGVSp=ENSP00000466777.1:p.Gly67Val,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=2/7,cDNA_position=199,CDS_position=200,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=67,Codons=gGc/gTc,MINIMISED=1,HGVSc=ENST00000585561.1:c.199G>T
CDS|ENST00000585561	VCF	missense_variant	216	216	0.0	.	.	AC_Male=1;AF_NFE=2.58685e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-31;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.06140e-05;Hom=0;AF_POPMAX=2.58685e-05;AN_POPMAX=77314;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=9.69330e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.87363e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.17280e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.91480e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.21760e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.13),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.053),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/S,HGVSp=ENSP00000466777.1:p.Ala73Ser,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=2/7,cDNA_position=216,CDS_position=217,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=73,Codons=Gcc/Tcc,MINIMISED=1,HGVSc=ENST00000585561.1:c.216G>T
CDS|ENST00000585561	VCF	missense_variant	217	217	0.0	.	.	AC_Male=0;AF_NFE=1.30774e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.34920e-06;Hom=0;AF_POPMAX=1.30774e-05;AN_POPMAX=76468;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.84615e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=65;AF_Female=1.18189e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.26907e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10985e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.28),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.079),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=A/V,HGVSp=ENSP00000466777.1:p.Ala73Val,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=2/7,cDNA_position=217,CDS_position=218,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=73,Codons=gCc/gTc,MINIMISED=1,HGVSc=ENST00000585561.1:c.217C>T
CDS|ENST00000585561	VCF	missense_variant	221	221	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-72;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.55759e-06;Hom=0;AF_POPMAX=3.91972e-05;AN_POPMAX=25512;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.22730e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.91972e-05;AS_RF=8.51470e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11306e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.02),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=possibly_damaging(0.8),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Q/H,HGVSp=ENSP00000466777.1:p.Gln74His,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=2/7,cDNA_position=221,CDS_position=222,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=74,Codons=caG/caC,MINIMISED=1,HGVSc=ENST00000585561.1:c.221G>C
CDS|ENST00000585561	VCF	missense_variant	225	225	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=70;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97133e-05;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.12740e-05;Hom=0;AF_POPMAX=8.46453e-05;AN_POPMAX=11814;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.03086e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.94118e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=1.24387e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.04301e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=8.46453e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.23113e-06;Hom_Female=0;AF_AMR=3.93236e-05;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=probably_damaging(0.979),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Q/K,HGVSp=ENSP00000466777.1:p.Gln76Lys,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=2/7,cDNA_position=225,CDS_position=226,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=76,Codons=Cag/Aag,MINIMISED=1,HGVSc=ENST00000585561.1:c.225C>A
CDS|ENST00000585561	VCF	missense_variant	231	231	0.0	.	.	AC_Male=1;AF_NFE=2.98686e-05;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|2|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.19832e-05;Hom=0;AF_POPMAX=2.98686e-05;AN_POPMAX=66960;AC_NFE=2;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.09965e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.15047e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.31645e-05;GQ_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.22455e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64978e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious_low_confidence(0.01),UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:2.776e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:5.974e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.066),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=V/M,HGVSp=ENSP00000466777.1:p.Val78Met,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=2/7,ExAC_AMR_MAF=A:0,cDNA_position=231,CDS_position=232,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761306458,VARIANT_CLASS=SNV,Protein_position=78,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.569e-06,HGVSc=ENST00000585561.1:c.231G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	missense_variant	248	248	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=9;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.38684e-02;AF_OTH=.;alleles=G%2CT;AF_FIN=.;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=.;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=.;DP_MEDIAN=7;AF_Female=0.00000e+00;GQ_HIST_ALT=0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=1;AF_SAS=.;AS_RF=8.18793e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=.;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.32474e-04;Hom_Female=0;AF_AMR=.;CSQ=ALLELE_NUM=1,SIFT=tolerated_low_confidence(0.72),UNIPARC=UPI0002841053,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_start_NF,Feature_type=Transcript,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,Consequence=missense_variant&NMD_transcript_variant,Amino_acids=Q/H,HGVSp=ENSP00000466777.1:p.Gln83His,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=3/7,cDNA_position=248,CDS_position=249,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=83,Codons=caG/caT,MINIMISED=1,HGVSc=ENST00000585561.1:c.248G>T
CDS|ENST00000585561	dbSNP	sequence_variant	1	1	0.0	+	.	consequence_type=missense_variant;id=rs771527303;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	3	3	0.0	+	.	consequence_type=missense_variant;id=rs772761859;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	4	4	0.0	+	.	consequence_type=missense_variant;id=rs1317068708;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	6	6	0.0	+	.	consequence_type=missense_variant;id=rs983223652;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	7	7	0.0	+	.	consequence_type=missense_variant;id=rs760309598;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	9	9	0.0	+	.	consequence_type=missense_variant;id=rs564172691;alleles=A%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	10	10	0.0	+	.	consequence_type=missense_variant;id=rs1314954450;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	11	11	0.0	+	.	consequence_type=synonymous_variant;id=rs1009445042;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	12	12	0.0	+	.	consequence_type=missense_variant;id=rs267604914;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	14	14	0.0	+	.	consequence_type=synonymous_variant;id=rs776210749;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	15	15	0.0	+	.	consequence_type=missense_variant;id=rs1292079143;alleles=A%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	16	16	0.0	+	.	consequence_type=missense_variant;id=rs1022554088;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	17	17	0.0	+	.	consequence_type=synonymous_variant;id=rs763334167;alleles=A%2CC%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	18	18	0.0	+	.	consequence_type=missense_variant;id=rs907713546;alleles=G%2CA%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	19	19	0.0	+	.	consequence_type=missense_variant;id=rs764406772;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	20	20	0.0	+	.	consequence_type=synonymous_variant;id=rs1253429311;alleles=A%2CC%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	21	21	0.0	+	.	consequence_type=missense_variant;id=rs752105945;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	26	26	0.0	+	.	consequence_type=synonymous_variant;id=rs757761311;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	27	27	0.0	+	.	consequence_type=missense_variant;id=rs767553043;alleles=C%2CA%2CG%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	28	28	0.0	+	.	consequence_type=missense_variant;id=rs750513385;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	29	29	0.0	+	.	consequence_type=synonymous_variant;id=rs1007666082;alleles=G%2CA%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	30	45	0.0	+	.	consequence_type=frameshift_variant;id=rs1306813664;alleles=CCGGCACCTCCGCTGC%2C-
CDS|ENST00000585561	dbSNP	sequence_variant	46	46	0.0	+	.	consequence_type=missense_variant;id=rs937347334;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	50	50	0.0	+	.	consequence_type=synonymous_variant;id=rs1229832497;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	52	52	0.0	+	.	consequence_type=missense_variant;id=rs1315229471;alleles=T%2CC%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	55	55	0.0	+	.	consequence_type=missense_variant;id=rs772952636;alleles=T%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	59	60	0.0	+	.	consequence_type=inframe_insertion;id=rs1219870401;alleles=-%2CGGGAAC
CDS|ENST00000585561	dbSNP	sequence_variant	66	66	0.0	+	.	consequence_type=missense_variant;id=rs746539074;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	67	67	0.0	+	.	consequence_type=missense_variant;id=rs1437942507;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	69	70	0.0	+	.	consequence_type=inframe_insertion;id=rs763191382;alleles=-%2CACGGCC
CDS|ENST00000585561	dbSNP	sequence_variant	72	72	0.0	+	.	consequence_type=missense_variant;id=rs770300796;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	73	73	0.0	+	.	consequence_type=missense_variant;id=rs1451260585;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	76	76	0.0	+	.	consequence_type=missense_variant;id=rs1362841019;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	77	77	0.0	+	.	consequence_type=missense_variant;id=rs776300314;alleles=T%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	78	78	0.0	+	.	consequence_type=missense_variant;id=rs1159616651;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	79	79	0.0	+	.	consequence_type=missense_variant;id=rs1185809906;alleles=A%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	83	83	0.0	+	.	consequence_type=missense_variant;id=rs759161485;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	85	85	0.0	+	.	consequence_type=missense_variant;id=rs764495116;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	87	87	0.0	+	.	consequence_type=missense_variant;id=rs774684452;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	90	90	0.0	+	.	consequence_type=missense_variant;id=rs976121906;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	94	94	0.0	+	.	consequence_type=missense_variant;id=rs895881728;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	95	95	0.0	+	.	consequence_type=missense_variant;id=rs762294220;alleles=C%2CG%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	98	98	0.0	+	.	consequence_type=synonymous_variant;id=rs768076232;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	107	107	0.0	+	.	consequence_type=synonymous_variant;id=rs1328029981;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	116	116	0.0	+	.	consequence_type=missense_variant;id=rs750844557;alleles=C%2CG%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	118	118	0.0	+	.	consequence_type=missense_variant;id=rs756247053;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	120	122	0.0	+	.	consequence_type=inframe_deletion;id=rs375981533;alleles=AAC%2C-
CDS|ENST00000585561	dbSNP	sequence_variant	124	124	0.0	+	.	consequence_type=missense_variant;id=rs1271597368;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	125	125	0.0	+	.	consequence_type=splice_region_variant;id=rs143955814;alleles=G%2CA%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	130	130	0.0	+	.	consequence_type=missense_variant;id=rs752810524;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	132	132	0.0	+	.	consequence_type=missense_variant;id=rs758247752;alleles=T%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	133	133	0.0	+	.	consequence_type=missense_variant;id=rs1199096532;alleles=T%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	136	136	0.0	+	.	consequence_type=missense_variant;id=rs1286861992;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	137	137	0.0	+	.	consequence_type=synonymous_variant;id=rs777402320;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	138	138	0.0	+	.	consequence_type=missense_variant;id=rs1192808116;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	139	139	0.0	+	.	consequence_type=missense_variant;id=rs1212522731;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	144	144	0.0	+	.	consequence_type=missense_variant;id=rs140455291;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	145	145	0.0	+	.	consequence_type=missense_variant;id=rs757177482;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	157	157	0.0	+	.	consequence_type=missense_variant;id=rs780748535;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	160	160	0.0	+	.	consequence_type=missense_variant;id=rs774451911;alleles=A%2CG%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	172	172	0.0	+	.	consequence_type=missense_variant;id=rs1468231466;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	177	177	0.0	+	.	consequence_type=missense_variant;id=rs3087878;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	182	182	0.0	+	.	consequence_type=synonymous_variant;id=rs375158125;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	187	187	0.0	+	.	consequence_type=missense_variant;id=rs201559014;alleles=A%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	189	189	0.0	+	.	consequence_type=missense_variant;id=rs779784731;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	197	197	0.0	+	.	consequence_type=synonymous_variant;id=rs141656657;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	199	199	0.0	+	.	consequence_type=missense_variant;id=rs1399730029;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	200	200	0.0	+	.	consequence_type=synonymous_variant;id=rs1315823029;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	206	206	0.0	+	.	consequence_type=synonymous_variant;id=rs369434915;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	216	216	0.0	+	.	consequence_type=missense_variant;id=rs1405046109;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	217	217	0.0	+	.	consequence_type=missense_variant;id=rs1284414737;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	218	218	0.0	+	.	consequence_type=synonymous_variant;id=rs184508172;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	221	221	0.0	+	.	consequence_type=missense_variant;id=rs1231776580;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	225	225	0.0	+	.	consequence_type=missense_variant;id=rs1281614790;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	231	231	0.0	+	.	consequence_type=missense_variant;id=rs761306458;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	239	239	0.0	+	.	consequence_type=splice_region_variant;id=rs1186056068;alleles=T%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	248	248	0.0	+	.	consequence_type=missense_variant;id=rs1156392845;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	254	254	0.0	+	.	consequence_type=synonymous_variant;id=rs1004120445;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	255	255	0.0	+	.	consequence_type=missense_variant;id=rs190843751;alleles=G%2CA%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	261	261	0.0	+	.	consequence_type=missense_variant;id=rs1016902129;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	268	268	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs760933047;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	269	269	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs963036023;alleles=G%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	273	273	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs980855707;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	274	274	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs771118685;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	277	277	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs932794908;alleles=A%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	283	283	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1272891946;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	288	288	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1214718483;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	291	291	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1363368716;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	296	296	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs369898370;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	306	306	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1424975428;alleles=C%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	312	312	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs910292120;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	316	316	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs2106354;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	317	317	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1460258950;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	324	324	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs1040082735;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	325	325	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs2027994;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	331	331	0.0	+	.	consequence_type=3_prime_UTR_variant;id=rs763994866;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	332	332	0.0	+	.	consequence_type=splice_region_variant;id=rs945601080;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	333	333	0.0	+	.	consequence_type=splice_region_variant;id=rs979686400;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	335	335	0.0	+	.	consequence_type=start_lost;id=rs767459577;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	339	339	0.0	+	.	consequence_type=missense_variant;id=rs367954716;alleles=A%2CC%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	343	343	0.0	+	.	consequence_type=synonymous_variant;id=rs200633656;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	346	346	0.0	+	.	consequence_type=missense_variant;id=rs1018863986;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	355	355	0.0	+	.	consequence_type=missense_variant;id=rs1051019368;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	361	361	0.0	+	.	consequence_type=missense_variant;id=rs779405921;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	367	367	0.0	+	.	consequence_type=synonymous_variant;id=rs1382805858;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	380	380	0.0	+	.	consequence_type=missense_variant;id=rs1463089836;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	381	381	0.0	+	.	consequence_type=missense_variant;id=rs1308984921;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	382	382	0.0	+	.	consequence_type=synonymous_variant;id=rs372318247;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	388	388	0.0	+	.	consequence_type=synonymous_variant;id=rs754577624;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	394	394	0.0	+	.	consequence_type=synonymous_variant;id=rs1391388443;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	396	396	0.0	+	.	consequence_type=missense_variant;id=rs778561485;alleles=T%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	398	398	0.0	+	.	consequence_type=missense_variant;id=rs747390700;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	402	402	0.0	+	.	consequence_type=missense_variant;id=rs1335366133;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	403	403	0.0	+	.	consequence_type=missense_variant;id=rs771371139;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	404	404	0.0	+	.	consequence_type=missense_variant;id=rs563736659;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	406	406	0.0	+	.	consequence_type=synonymous_variant;id=rs746348189;alleles=A%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	407	407	0.0	+	.	consequence_type=missense_variant;id=rs1294041634;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	408	408	0.0	+	.	consequence_type=missense_variant;id=rs1416691571;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	410	410	0.0	+	.	consequence_type=missense_variant;id=rs868718436;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	412	412	0.0	+	.	consequence_type=synonymous_variant;id=rs1229714849;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	419	419	0.0	+	.	consequence_type=missense_variant;id=rs1348860194;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	420	420	0.0	+	.	consequence_type=missense_variant;id=rs770043528;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	426	426	0.0	+	.	consequence_type=missense_variant;id=rs775419569;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	427	427	0.0	+	.	consequence_type=synonymous_variant;id=rs972147914;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	428	428	0.0	+	.	consequence_type=missense_variant;id=rs1297768336;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	429	429	0.0	+	.	consequence_type=missense_variant;id=rs1443418786;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	430	430	0.0	+	.	consequence_type=synonymous_variant;id=rs1338651806;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	431	431	0.0	+	.	consequence_type=missense_variant;id=rs1196722115;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	433	433	0.0	+	.	consequence_type=synonymous_variant;id=rs1244710451;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	438	438	0.0	+	.	consequence_type=missense_variant;id=rs377156745;alleles=G%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	440	440	0.0	+	.	consequence_type=missense_variant;id=rs1182546534;alleles=A%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	447	447	0.0	+	.	consequence_type=missense_variant;id=rs1391284036;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	451	451	0.0	+	.	consequence_type=synonymous_variant;id=rs1253657974;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	459	459	0.0	+	.	consequence_type=missense_variant;id=rs764230766;alleles=C%2CG%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	460	460	0.0	+	.	consequence_type=synonymous_variant;id=rs1170526700;alleles=G%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	466	466	0.0	+	.	consequence_type=synonymous_variant;id=rs774578466;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	467	467	0.0	+	.	consequence_type=missense_variant;id=rs761622308;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	472	472	0.0	+	.	consequence_type=synonymous_variant;id=rs767261647;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	474	474	0.0	+	.	consequence_type=missense_variant;id=rs144433221;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	481	481	0.0	+	.	consequence_type=splice_region_variant;id=rs199678185;alleles=C%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	486	486	0.0	+	.	consequence_type=missense_variant;id=rs1216003679;alleles=T%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	493	493	0.0	+	.	consequence_type=synonymous_variant;id=rs760391896;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	496	496	0.0	+	.	consequence_type=synonymous_variant;id=rs766241230;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	497	497	0.0	+	.	consequence_type=missense_variant;id=rs753759265;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	502	502	0.0	+	.	consequence_type=synonymous_variant;id=rs1269052802;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	505	505	0.0	+	.	consequence_type=synonymous_variant;id=rs147841016;alleles=C%2CG%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	506	506	0.0	+	.	consequence_type=missense_variant;id=rs752448187;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	511	511	0.0	+	.	consequence_type=synonymous_variant;id=rs1250252141;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	512	512	0.0	+	.	consequence_type=missense_variant;id=rs758111913;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	513	513	0.0	+	.	consequence_type=missense_variant;id=rs1421268751;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	515	515	0.0	+	.	consequence_type=missense_variant;id=rs201386803;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	517	517	0.0	+	.	consequence_type=synonymous_variant;id=rs535242567;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	518	518	0.0	+	.	consequence_type=missense_variant;id=rs986408291;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	520	520	0.0	+	.	consequence_type=synonymous_variant;id=rs1418173661;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	531	531	0.0	+	.	consequence_type=missense_variant;id=rs955288678;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	532	532	0.0	+	.	consequence_type=synonymous_variant;id=rs1456376961;alleles=C%2CG%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	533	533	0.0	+	.	consequence_type=missense_variant;id=rs1161073719;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	536	536	0.0	+	.	consequence_type=missense_variant;id=rs1305018160;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	538	538	0.0	+	.	consequence_type=synonymous_variant;id=rs910463482;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	539	539	0.0	+	.	consequence_type=missense_variant;id=rs1366323829;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	554	554	0.0	+	.	consequence_type=stop_gained;id=rs1435626124;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	557	557	0.0	+	.	consequence_type=missense_variant;id=rs1291739811;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	565	565	0.0	+	.	consequence_type=synonymous_variant;id=rs559376009;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	575	575	0.0	+	.	consequence_type=synonymous_variant;id=rs1199425750;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	581	581	0.0	+	.	consequence_type=synonymous_variant;id=rs1132898;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	583	583	0.0	+	.	consequence_type=synonymous_variant;id=rs1306112590;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	586	586	0.0	+	.	consequence_type=synonymous_variant;id=rs749766632;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	587	587	0.0	+	.	consequence_type=missense_variant;id=rs149737135;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	590	590	0.0	+	.	consequence_type=missense_variant;id=rs778948844;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	591	591	0.0	+	.	consequence_type=missense_variant;id=rs748432196;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	592	592	0.0	+	.	consequence_type=synonymous_variant;id=rs1221407945;alleles=T%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	593	593	0.0	+	.	consequence_type=missense_variant;id=rs1269207571;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	595	595	0.0	+	.	consequence_type=synonymous_variant;id=rs772281237;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	596	596	0.0	+	.	consequence_type=missense_variant;id=rs773364852;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	608	608	0.0	+	.	consequence_type=missense_variant;id=rs1377176181;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	616	616	0.0	+	.	consequence_type=missense_variant;id=rs770678984;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	622	622	0.0	+	.	consequence_type=missense_variant;id=rs927057705;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	634	634	0.0	+	.	consequence_type=synonymous_variant;id=rs151247418;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	649	649	0.0	+	.	consequence_type=synonymous_variant;id=rs776474941;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	652	652	0.0	+	.	consequence_type=synonymous_variant;id=rs1410437263;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	653	653	0.0	+	.	consequence_type=missense_variant;id=rs1283407561;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	664	664	0.0	+	.	consequence_type=synonymous_variant;id=rs759459614;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	673	673	0.0	+	.	consequence_type=synonymous_variant;id=rs372926712;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	675	675	0.0	+	.	consequence_type=missense_variant;id=rs775510228;alleles=C%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	676	676	0.0	+	.	consequence_type=synonymous_variant;id=rs146345914;alleles=G%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	677	677	0.0	+	.	consequence_type=missense_variant;id=rs1339503876;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	678	678	0.0	+	.	consequence_type=missense_variant;id=rs1445433341;alleles=A%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	679	679	0.0	+	.	consequence_type=missense_variant;id=rs866488889;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	680	680	0.0	+	.	consequence_type=missense_variant;id=rs1311826897;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	686	686	0.0	+	.	consequence_type=synonymous_variant;id=rs1259891285;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	698	698	0.0	+	.	consequence_type=missense_variant;id=rs764148755;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	699	699	0.0	+	.	consequence_type=missense_variant;id=rs150418753;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	706	706	0.0	+	.	consequence_type=synonymous_variant;id=rs757227703;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	707	707	0.0	+	.	consequence_type=missense_variant;id=rs781499966;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	712	712	0.0	+	.	consequence_type=missense_variant;id=rs746041079;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	713	713	0.0	+	.	consequence_type=missense_variant;id=rs756018179;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	715	715	0.0	+	.	consequence_type=synonymous_variant;id=rs369385342;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	717	717	0.0	+	.	consequence_type=missense_variant;id=rs779975972;alleles=C%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	733	733	0.0	+	.	consequence_type=synonymous_variant;id=rs768715452;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	743	743	0.0	+	.	consequence_type=missense_variant;id=rs774095582;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	745	745	0.0	+	.	consequence_type=synonymous_variant;id=rs199671891;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	751	751	0.0	+	.	consequence_type=synonymous_variant;id=rs112989351;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	752	752	0.0	+	.	consequence_type=missense_variant;id=rs1407256029;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	753	753	0.0	+	.	consequence_type=missense_variant;id=rs771441667;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	754	754	0.0	+	.	consequence_type=synonymous_variant;id=rs1330823537;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	757	757	0.0	+	.	consequence_type=synonymous_variant;id=rs1259991653;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	772	772	0.0	+	.	consequence_type=missense_variant;id=rs1303544092;alleles=T%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	773	773	0.0	+	.	consequence_type=missense_variant;id=rs919282095;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	775	775	0.0	+	.	consequence_type=synonymous_variant;id=rs772957252;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	781	781	0.0	+	.	consequence_type=missense_variant;id=rs375089291;alleles=C%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	784	784	0.0	+	.	consequence_type=synonymous_variant;id=rs770200317;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	795	795	0.0	+	.	consequence_type=missense_variant;id=rs775829411;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	801	801	0.0	+	.	consequence_type=missense_variant;id=rs763238851;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	802	802	0.0	+	.	consequence_type=synonymous_variant;id=rs1490869430;alleles=T%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	806	806	0.0	+	.	consequence_type=missense_variant;id=rs1342497115;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	807	807	0.0	+	.	consequence_type=missense_variant;id=rs764674925;alleles=C%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	31	31	0.0	+	.	consequence_type=missense_variant;id=rs756082410;alleles=C%2CA%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	32	32	0.0	+	.	consequence_type=synonymous_variant;id=rs780444510;alleles=G%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	33	33	0.0	+	.	consequence_type=missense_variant;id=rs1424340537;alleles=G%2CC
CDS|ENST00000585561	dbSNP	sequence_variant	34	34	0.0	+	.	consequence_type=missense_variant;id=rs973343235;alleles=C%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	36	36	0.0	+	.	consequence_type=missense_variant;id=rs754859910;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	37	37	0.0	+	.	consequence_type=missense_variant;id=rs1356403688;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	40	40	0.0	+	.	consequence_type=missense_variant;id=rs202061902;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	42	42	0.0	+	.	consequence_type=synonymous_variant;id=rs748150811;alleles=C%2CT
CDS|ENST00000585561	dbSNP	sequence_variant	43	43	0.0	+	.	consequence_type=missense_variant;id=rs772038652;alleles=T%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	44	44	0.0	+	.	consequence_type=synonymous_variant;id=rs927228181;alleles=G%2CA
CDS|ENST00000585561	dbSNP	sequence_variant	118	120	0.0	+	.	consequence_type=inframe_deletion;id=rs766213031;alleles=ACA%2C-
CDS|ENST00000585561	dbSNP	sequence_variant	121	121	0.0	+	.	consequence_type=missense_variant;id=rs946116469;alleles=A%2CG
CDS|ENST00000585561	dbSNP	sequence_variant	122	122	0.0	+	.	consequence_type=synonymous_variant;id=rs766535198;alleles=C%2CT
CDS|ENST00000585561	VCF	3_prime_UTR_variant	306	306	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=21;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.04774e-04;AF_OTH=.;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=.;DP_MEDIAN=3;AF_Female=0.00000e+00;GQ_HIST_ALT=0|1|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=1;AF_SAS=.;AS_RF=5.22057e-02;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=.;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.19990e-04;Hom_Female=0;AF_AMR=.;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=3/7,cDNA_position=306,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*40C>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	339	339	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51591e-22;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.09459e-05;AN_POPMAX=16408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.23913e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20091e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.09459e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.391e-06,ExAC_MAF=T:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=C,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=339,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*73A>C,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	339	339	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-62;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.67646e-05;AN_POPMAX=14978;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.67646e-05;AC_raw=1;AB_MEDIAN=3.09859e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.02337e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.391e-06,ExAC_MAF=T:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=T,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=339,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*73A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	343	343	0.0	.	.	AC_Male=0;AF_NFE=9.11594e-06;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15014e-06;Hom=0;AF_POPMAX=9.11594e-06;AN_POPMAX=109698;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.77778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=9.19912e-06;GQ_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.62962e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.372e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.518e-05,AFR_MAF=C:0,FLAGS=cds_start_NF,EAS_MAF=C:0,EUR_MAF=C:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=C:0.0002,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=C:0,cDNA_position=343,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs200633656,SAS_MAF=C:0.001,VARIANT_CLASS=SNV,AA_MAF=C:0,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*77T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	361	361	0.0	.	.	AC_Male=1;AF_NFE=9.04977e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-52;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10988e-06;Hom=0;AF_POPMAX=9.04977e-06;AN_POPMAX=110500;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49524e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.10256e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.90362e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.312e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.51e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=G:0,cDNA_position=361,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779405921,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.*95C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	367	367	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|2|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22868e-05;Hom=0;AF_POPMAX=9.08045e-05;AN_POPMAX=33038;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46949e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=6.81818e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.81347e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.72461e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=9.08045e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=4/7,cDNA_position=367,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*101A>G
CDS|ENST00000585561	VCF	3_prime_UTR_variant	380	380	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-21;AF_OTH=1.83554e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08013e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.70588e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=9.03130e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.67445e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=4/7,cDNA_position=380,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*114A>G
CDS|ENST00000585561	VCF	3_prime_UTR_variant	382	382	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-142;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07917e-06;Hom=0;AF_POPMAX=6.55996e-05;AN_POPMAX=15244;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=6.55996e-05;AC_raw=1;AB_MEDIAN=4.83146e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.02657e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.95139e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.272e-06,ExAC_MAF=C:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,EA_MAF=C:0.0002,Allele=C,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=C:9.641e-05,cDNA_position=382,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs372318247,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*116T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	388	388	0.0	.	.	AC_Male=1;AF_NFE=8.97747e-06;Hom_FIN=0;GQ_MEDIAN=73;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97611e-06;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14538e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.54779e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.00868e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.44770e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.266e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:0,cDNA_position=388,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754577624,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*122G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	394	394	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07193e-06;Hom=0;AF_POPMAX=3.25457e-05;AN_POPMAX=30726;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43141e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25457e-05;AS_RF=8.52320e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=4/7,cDNA_position=394,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*128A>G
CDS|ENST00000585561	VCF	3_prime_UTR_variant	396	396	0.0	.	.	AC_Male=0;AF_NFE=8.97263e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-62;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07163e-06;Hom=0;AF_POPMAX=8.97263e-06;AN_POPMAX=111450;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=48;AF_Female=9.00739e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.258e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=A:0,cDNA_position=396,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs778561485,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*130T>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	398	398	0.0	.	.	AC_Male=0;AF_NFE=8.97167e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-66;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07073e-06;Hom=0;AF_POPMAX=8.97167e-06;AN_POPMAX=111462;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.45455e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00414e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97942e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.258e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:0,cDNA_position=398,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs747390700,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*132G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	403	403	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-48;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07186e-06;Hom=0;AF_POPMAX=3.25563e-05;AN_POPMAX=30716;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43097e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25563e-05;AS_RF=9.07079e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.256e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=C:0,cDNA_position=403,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs771371139,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*137G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	404	404	0.0	.	.	AC_Male=1;AF_NFE=8.97392e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07279e-06;Hom=0;AF_POPMAX=8.97392e-06;AN_POPMAX=111434;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43152e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.97872e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.42544e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=A:8.254e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=A:0,cDNA_position=404,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs563736659&COSM1493963,SAS_MAF=A:0.001,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*138G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	406	406	0.0	.	.	AC_Male=1;AF_NFE=8.99006e-06;Hom_FIN=0;GQ_MEDIAN=34;AB_HIST_ALT=0|0|0|0|4|3|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=4.08532e-04;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=1.35404e-04;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44760e-05;Hom=0;AF_POPMAX=1.35404e-04;AN_POPMAX=22156;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.44114e-06;AF_AFR=1.31406e-04;AC_raw=8;AB_MEDIAN=2.47642e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=4.51467e-05;GQ_HIST_ALT=0|1|1|0|0|1|1|1|0|0|1|0|1|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.54316e-03;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:6.621e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:6.02e-05,AFR_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=C:0.0002899,cDNA_position=406,ExAC_NFE_MAF=C:0.0001537,SYMBOL=NMT1,Existing_variation=rs746348189,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:9.060e-05,HGVSc=ENST00000585561.1:c.*140A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	412	412	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07701e-06;Hom=0;AF_POPMAX=3.25945e-05;AN_POPMAX=30680;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25945e-05;AS_RF=8.53172e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=4/7,cDNA_position=412,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*146C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	420	420	0.0	.	.	AC_Male=1;AF_NFE=8.98053e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-63;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07515e-06;Hom=0;AF_POPMAX=8.98053e-06;AN_POPMAX=111352;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43528e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.03846e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=52;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18859e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.249e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.501e-05,AFR_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=C:0,cDNA_position=420,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs770043528,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*154T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	430	430	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-42;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07501e-06;Hom=0;AF_POPMAX=2.99419e-05;AN_POPMAX=33398;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43450e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.92593e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.81783e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99419e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=4/7,cDNA_position=430,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*164T>C
CDS|ENST00000585561	VCF	3_prime_UTR_variant	431	431	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=7.94328e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=4.48632e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07581e-06;Hom=0;AF_POPMAX=4.48632e-05;AN_POPMAX=22290;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43572e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.25000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.10681e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=4/7,cDNA_position=431,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*165A>G
CDS|ENST00000585561	VCF	3_prime_UTR_variant	433	433	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07465e-06;Hom=0;AF_POPMAX=2.99455e-05;AN_POPMAX=33394;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.67568e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=37;AF_Female=9.01518e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92008e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99455e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=4/7,cDNA_position=433,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*167C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	438	438	0.0	.	.	AC_Male=1;AF_NFE=1.79727e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-36;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15328e-06;Hom=0;AF_POPMAX=1.79727e-05;AN_POPMAX=111280;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=9.02120e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.61453e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=T:8.259e-06,ExAC_MAF=T:0.0001,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:0,cDNA_position=438,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs377156745&COSM436718,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*172G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	440	440	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07525e-06;Hom=0;AF_POPMAX=3.25839e-05;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43550e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25839e-05;AS_RF=7.10677e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=4/7,cDNA_position=440,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*174A>C
CDS|ENST00000585561	VCF	3_prime_UTR_variant	451	451	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=25;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15231e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=8;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66799e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=4/7,cDNA_position=451,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*185C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	459	459	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.91433e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.37719e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.02383e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:0,cDNA_position=459,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*193C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	459	459	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-14;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.51858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=G,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:0,cDNA_position=459,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*193C>G,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	460	460	0.0	.	.	AC_Male=0;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-30;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.78261e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=9.08364e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.39564e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=4/7,cDNA_position=460,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,HGVSc=ENST00000585561.1:c.*194G>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	460	460	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|1|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.69441e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=3.02810e-05;AN_POPMAX=33024;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|3|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48671e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=1.60256e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.95538e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=3.02810e-05;CSQ=ALLELE_NUM=2,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=4/7,cDNA_position=460,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,HGVSc=ENST00000585561.1:c.*194G>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	466	466	0.0	.	.	AC_Male=13;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|2|0|5|2|0|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=15;Hom_NFE=0;AF=6.19001e-05;Hom=0;AF_POPMAX=4.28788e-04;AN_POPMAX=30318;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|4|2|1|1|1|0|1|0|0|2|1|0|0|1|0|0;AF_Male=9.78076e-05;AF_AFR=6.60153e-05;AC_raw=15;AB_MEDIAN=4.72797e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.82795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|15;Hom_raw=0;AF_SAS=4.28788e-04;AS_RF=9.33794e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.89692e-05;AC_SAS=13;POPMAX=SAS;AC_POPMAX=13;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09088e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.385e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0005311,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=T:9.632e-05,cDNA_position=466,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs774578466,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-05,HGVSc=ENST00000585561.1:c.*200C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	467	467	0.0	.	.	AC_Male=0;AF_NFE=9.10167e-06;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|2|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13213e-06;Hom=0;AF_POPMAX=9.10167e-06;AN_POPMAX=109870;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=9.15131e-06;GQ_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.57813e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.387e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=A:0,cDNA_position=467,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761622308,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*201G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	472	472	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-31;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13839e-06;Hom=0;AF_POPMAX=3.31279e-05;AN_POPMAX=30186;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.54523e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.58333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.31279e-05;AS_RF=8.33412e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.422e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=G:0,cDNA_position=472,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767261647,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.*206C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	474	474	0.0	.	.	AC_Male=5;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|5|2|2|3|0|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-65;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.79897e-05;Hom=0;AF_POPMAX=9.23483e-04;AN_POPMAX=15160;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|3|1|1|1|0|0|0|0|1|1|1|2|0|1|0|1|1|1;AF_Male=3.77729e-05;AF_AFR=9.23483e-04;AC_raw=15;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=8.25294e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36291e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=14;AC_AFR=14;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:0.0001096,ExAC_MAF=G:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0.0014,Allele=G,IMPACT=MODIFIER,EXON=4/7,ExAC_AMR_MAF=G:0.001254,cDNA_position=474,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs144433221,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:1.071e-04,HGVSc=ENST00000585561.1:c.*208A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	486	486	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-43;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06782e-06;Hom=0;AF_POPMAX=3.24950e-05;AN_POPMAX=30774;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42677e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.40426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24950e-05;AS_RF=7.83979e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=5/7,cDNA_position=486,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*220T>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	493	493	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06669e-06;Hom=0;AF_POPMAX=3.24971e-05;AN_POPMAX=30772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42501e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24971e-05;AS_RF=9.28048e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.289e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:0,cDNA_position=493,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs760391896,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000585561.1:c.*227C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	496	496	0.0	.	.	AC_Male=1;AF_NFE=8.97054e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-32;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06544e-06;Hom=0;AF_POPMAX=8.97054e-06;AN_POPMAX=111476;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.48276e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.93308e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.285e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.508e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=A:0,cDNA_position=496,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs766241230,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000585561.1:c.*230C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	497	497	0.0	.	.	AC_Male=1;AF_NFE=1.79398e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-64;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13028e-06;Hom=0;AF_POPMAX=1.79398e-05;AN_POPMAX=111484;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0;AF_Male=7.42148e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.25373e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=67;AF_Female=8.98876e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13408e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.657e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.015e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:0,cDNA_position=497,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs753759265,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.*231C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	502	502	0.0	.	.	AC_Male=0;AF_NFE=8.97022e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-93;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06521e-06;Hom=0;AF_POPMAX=8.97022e-06;AN_POPMAX=111480;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.90164e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98779e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40909e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=5/7,cDNA_position=502,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*236C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	505	505	0.0	.	.	AC_Male=22;AF_NFE=2.68986e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|9|6|8|6|4|1|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.00000e-61;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=37;Hom_NFE=0;AF=1.50378e-04;Hom=0;AF_POPMAX=2.68986e-04;AN_POPMAX=111530;AC_NFE=30;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|6|3|4|4|5|5|3|2|0|2|3|0|0|0|0;AF_Male=1.63236e-04;AF_AFR=0.00000e+00;AC_raw=37;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=0.00000e+00;DP_MEDIAN=45;AF_Female=1.34805e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|37;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=30;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.50240e-04;Hom_Female=0;AF_AMR=1.78710e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,ExAC_MAF=G:0.0003,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0&G:0,EA_MAF=G:0.0002,Allele=G,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=505,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000585561.1:c.*239C>G,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000585561	VCF	3_prime_UTR_variant	505	505	0.0	.	.	AC_Male=4;AF_NFE=2.68986e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|3|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-59;AF_OTH=3.64830e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25142e-05;Hom=0;AF_POPMAX=1.30702e-04;AN_POPMAX=15302;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|1|1|2|2|0|0|0|0|0|0|0|0|0;AF_Male=2.96793e-05;AF_AFR=1.30702e-04;AC_raw=8;AB_MEDIAN=4.75384e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.59479e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=2;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,ExAC_MAF=G:0.0003,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0&G:0,EA_MAF=G:0.0002,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=505,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000585561.1:c.*239C>T,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000585561	VCF	3_prime_UTR_variant	506	506	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-36;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21939e-05;Hom=0;AF_POPMAX=1.15969e-04;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AF_Male=7.42027e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.77324e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=1.79762e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=3.24907e-05;AS_RF=8.84156e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.15969e-04;AC_SAS=1;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.272e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=A:0,cDNA_position=506,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs752448187,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000585561.1:c.*240G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	512	512	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-75;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06372e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.15584e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=8.98521e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.41661e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.265e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:0,cDNA_position=512,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs758111913,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*246C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	513	513	0.0	.	.	AC_Male=0;AF_NFE=8.96363e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-36;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06355e-06;Hom=0;AF_POPMAX=8.96363e-06;AN_POPMAX=111562;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41176e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00024e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=5/7,cDNA_position=513,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*247C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	515	515	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-72;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21915e-05;Hom=0;AF_POPMAX=1.73933e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|1|0|0|0|1|0|0|0|0|0|0;AF_Male=1.48381e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.76190e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98586e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=3;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.73933e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=A:1.653e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_start_NF,EAS_MAF=A:0,EUR_MAF=A:0.001,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0002313,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=A:0,cDNA_position=515,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs201386803&COSM349346,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000585561.1:c.*249G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	517	517	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06329e-06;Hom=0;AF_POPMAX=5.79845e-05;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53191e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50090e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79845e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.261e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,EAS_MAF=T:0,EUR_MAF=T:0.001,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001157,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=T:0.0002,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:0,cDNA_position=517,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs535242567,SAS_MAF=T:0,VARIANT_CLASS=SNV,AA_MAF=T:0,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*251C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	520	520	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-50;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06339e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41851e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43104e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=5/7,cDNA_position=520,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*254G>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	536	536	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-54;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62509e-05;Hom=0;AF_POPMAX=1.19119e-04;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|2|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41697e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.40000e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=2.69508e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99062e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=1.19119e-04;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=5/7,cDNA_position=536,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*270G>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	539	539	0.0	.	.	AC_Male=1;AF_NFE=8.96106e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-53;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06296e-06;Hom=0;AF_POPMAX=8.96106e-06;AN_POPMAX=111594;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41730e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.46809e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00924e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=5/7,cDNA_position=539,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*273C>G
CDS|ENST00000585561	VCF	3_prime_UTR_variant	554	554	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=3.98107e-106;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=4.48511e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06412e-06;Hom=0;AF_POPMAX=4.48511e-05;AN_POPMAX=22296;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41983e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.88235e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=68;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.32793e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=5/7,cDNA_position=554,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*288C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	557	557	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-51;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06398e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=7.41917e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.33333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=63;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=3.27293e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=5/7,cDNA_position=557,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*291G>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	565	565	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|2|0|1|2|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-64;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.84465e-05;Hom=0;AF_POPMAX=2.08445e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|0|1|0|2|0|1|0|0|1|0|0;AF_Male=1.48372e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=7;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=4.49317e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.52275e-01;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.84239e-05;Hom_Female=0;AF_AMR=2.08445e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:1.65e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=G:0,cDNA_position=565,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs559376009,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000585561.1:c.*299C>G,ExAC_Adj_MAF=G:0.0001732
CDS|ENST00000585561	VCF	3_prime_UTR_variant	581	581	0.0	.	.	AC_Male=25006;AF_NFE=2.09922e-01;Hom_FIN=285;GQ_MEDIAN=99;AB_HIST_ALT=0|0|5|15|72|453|1543|3857|7281|7755|7846|3986|1826|582|145|27|12|4|3|0;AC_FIN=3550;DREF_MEDIAN=1.00000e-73;AF_OTH=1.77555e-01;alleles=C%2CT;AF_FIN=1.59379e-01;AC_OTH=973;Hom_Male=2665;AC=45042;Hom_NFE=2465;AF=1.83181e-01;Hom=4839;AF_POPMAX=3.36036e-01;AN_POPMAX=15296;AC_NFE=23384;AS_FilterStatus=PASS;Hom_OTH=97;DP_HIST_ALT=2|26|94|195|538|1305|2559|3767|4480|4660|4316|3950|3356|2703|2157|1571|1256|914|624|548;AF_Male=1.85675e-01;AF_AFR=3.36036e-01;AC_raw=45128;AB_MEDIAN=4.75610e-01;Hom_EAS=11;AC_AMR=2943;AF_ASJ=1.65819e-01;DP_MEDIAN=52;AF_Female=1.80160e-01;GQ_HIST_ALT=6|6|7|9|6|14|13|17|10|21|33|20|43|66|53|88|83|83|130|39562;Hom_raw=4858;AF_SAS=2.21782e-01;AS_RF=9.54732e-01;Hom_AMR=167;AC_EAS=595;AC_Female=20036;Hom_AFR=875;Hom_ASJ=130;AF_EAS=3.44968e-02;AC_SAS=6826;POPMAX=AFR;AC_POPMAX=5140;AC_AFR=5140;Hom_SAS=809;AC_ASJ=1631;AF_raw=1.83246e-01;Hom_Female=2174;AF_AMR=8.76362e-02;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=T:0.1935,ExAC_MAF=T:0.2031,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=T:0.3616,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.2069,AFR_MAF=T:0.2226,FLAGS=cds_start_NF,EAS_MAF=T:0.134,EUR_MAF=T:0.0367,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0346,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=T:0.1991,STRAND=1,ExAC_SAS_MAF=T:0.1752,EA_MAF=T:0.325,SOMATIC=0&1,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:0.3348,cDNA_position=581,ExAC_NFE_MAF=T:0.1553,SYMBOL=NMT1,Existing_variation=rs1132898&COSM3755586,SAS_MAF=T:0.1769,VARIANT_CLASS=SNV,AA_MAF=T:0.2157,MINIMISED=1,ExAC_AFR_MAF=T:0.193,HGVSc=ENST00000585561.1:c.*315C>T,ExAC_Adj_MAF=T:0.08946
CDS|ENST00000585561	VCF	3_prime_UTR_variant	583	583	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-69;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06557e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.42280e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.31034e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=8.87045e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=5/7,cDNA_position=583,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*317G>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	586	586	0.0	.	.	AC_Male=2;AF_NFE=1.79498e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|2|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-46;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21991e-05;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|1;AF_Male=1.48469e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.69796e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=8.99184e-06;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.10458e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.652e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.006e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:0,cDNA_position=586,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs749766632,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.*320C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	587	587	0.0	.	.	AC_Male=12;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|1|0|2|2|2|2|6|13|4|3|2|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.90310e-58;AF_OTH=5.47445e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=3;Hom_Male=0;AC=37;Hom_NFE=0;AF=1.50482e-04;Hom=0;AF_POPMAX=2.09150e-03;AN_POPMAX=15300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|3|2|6|4|8|3|1|3|0|1|1|1|0|2|0|1;AF_Male=8.91080e-05;AF_AFR=2.09150e-03;AC_raw=38;AB_MEDIAN=4.66288e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=2.24804e-04;GQ_HIST_ALT=1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|36;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.44169e-01;Hom_AMR=0;AC_EAS=0;AC_Female=25;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=32;AC_AFR=32;Hom_SAS=0;AC_ASJ=0;AF_raw=1.54302e-04;Hom_Female=0;AF_AMR=5.95841e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:0.0001983,ExAC_MAF=A:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0.003,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_start_NF,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0010,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0.003,Allele=A,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=A:0.002214,cDNA_position=587,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs149737135,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,MINIMISED=1,ExAC_AFR_MAF=A:1.977e-04,HGVSc=ENST00000585561.1:c.*321G>A,ExAC_Adj_MAF=A:8.655e-05
CDS|ENST00000585561	VCF	3_prime_UTR_variant	590	590	0.0	.	.	AC_Male=0;AF_NFE=8.98101e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.50594e-44;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13524e-06;Hom=0;AF_POPMAX=2.97832e-05;AN_POPMAX=33576;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.33333e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=1.79863e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19608e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=2.97832e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=T:8.264e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.503e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=T:0,cDNA_position=590,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs778948844&COSM3518200,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*324C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	591	591	0.0	.	.	AC_Male=1;AF_NFE=1.79614e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-60;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13557e-06;Hom=0;AF_POPMAX=1.79614e-05;AN_POPMAX=111350;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.42721e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.70100e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=8.99329e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.19786e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.264e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.503e-05,AFR_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=C:0,cDNA_position=591,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs748432196,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*325G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	592	592	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-64;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06901e-06;Hom=0;AF_POPMAX=6.53595e-05;AN_POPMAX=15300;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53595e-05;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=46;AF_Female=8.99653e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.86417e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=G,IMPACT=MODIFIER,EXON=5/7,cDNA_position=592,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*326T>G
CDS|ENST00000585561	VCF	3_prime_UTR_variant	595	595	0.0	.	.	AC_Male=0;AF_NFE=8.98537e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-29;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06891e-06;Hom=0;AF_POPMAX=8.98537e-06;AN_POPMAX=111292;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.11111e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=18;AF_Female=8.99491e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.57047e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.267e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.503e-05,AFR_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=5/7,ExAC_AMR_MAF=C:0,cDNA_position=595,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs772281237,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*329T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	616	616	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|2|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16108e-109;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.24865e-05;Hom=0;AF_POPMAX=2.38223e-04;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|3|0|0|0|0|0|1|1;AF_Male=1.48258e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.25397e-01;Hom_EAS=0;AC_AMR=8;AF_ASJ=0.00000e+00;DP_MEDIAN=93;AF_Female=5.38812e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=6;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=8;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=2.38223e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:3.295e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=T:0,cDNA_position=616,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs770678984,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000585561.1:c.*350C>T,ExAC_Adj_MAF=T:0.0003455
CDS|ENST00000585561	VCF	3_prime_UTR_variant	649	649	0.0	.	.	AC_Male=4;AF_NFE=5.37095e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-123;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43643e-05;Hom=0;AF_POPMAX=5.37095e-05;AN_POPMAX=111712;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|1;AF_Male=2.96512e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.30292e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=135;AF_Female=1.79598e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:4.942e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.991e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=T:0,cDNA_position=649,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs776474941,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:4.942e-05,HGVSc=ENST00000585561.1:c.*383C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	652	652	0.0	.	.	AC_Male=0;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-101;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06068e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.05660e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=106;AF_Female=8.98005e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12871e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=6/7,cDNA_position=652,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*386C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	664	664	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-132;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.34426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=122;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.50786e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=C:0,cDNA_position=664,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs759459614,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*398T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	673	673	0.0	.	.	AC_Male=4;AF_NFE=1.16371e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|3|5|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-93;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=13;Hom_NFE=0;AF=5.27897e-05;Hom=0;AF_POPMAX=1.16371e-04;AN_POPMAX=111712;AC_NFE=13;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|2|1|1|0|0|1|0|0|1;AF_Male=2.96507e-05;AF_AFR=0.00000e+00;AC_raw=13;AB_MEDIAN=4.05405e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=97;AF_Female=8.08219e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|13;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.28067e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=13;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=5.27872e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:6.589e-05,ExAC_MAF=A:0.0001,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001199,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=A:0,cDNA_position=673,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs372926712,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:6.589e-05,HGVSc=ENST00000585561.1:c.*407C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	675	675	0.0	.	.	AC_Male=0;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-62;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=55;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99132e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=A,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=T:0,cDNA_position=675,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*409C>A,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	675	675	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-188;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=145;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=8.99177e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=T:0,cDNA_position=675,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs775510228,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*409C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	676	676	0.0	.	.	AC_Male=380;AF_NFE=2.32750e-03;Hom_FIN=3;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|2|40|88|203|202|119|49|4|0|0|0|0|0|0|0;AC_FIN=293;DREF_MEDIAN=5.01187e-117;AF_OTH=3.83072e-03;alleles=G%2CA;AF_FIN=1.31390e-02;AC_OTH=21;Hom_Male=2;AC=716;Hom_NFE=0;AF=2.90754e-03;Hom=4;AF_POPMAX=1.31390e-02;AN_POPMAX=22300;AC_NFE=260;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|5|6|15|17|25|30|39|50|52|47|44|38|56;AF_Male=2.81686e-03;AF_AFR=2.61370e-04;AC_raw=716;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=45;AF_ASJ=9.23858e-03;DP_MEDIAN=93;AF_Female=3.01740e-03;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|712;Hom_raw=4;AF_SAS=3.24865e-05;AS_RF=9.53701e-01;Hom_AMR=0;AC_EAS=1;AC_Female=336;Hom_AFR=0;Hom_ASJ=1;AF_EAS=5.79777e-05;AC_SAS=1;POPMAX=FIN;AC_POPMAX=293;AC_AFR=4;Hom_SAS=0;AC_ASJ=91;AF_raw=2.90735e-03;Hom_Female=2;AF_AMR=1.34000e-03;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:0.002586,ExAC_MAF=A:0.0022,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,FLAGS=cds_start_NF,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0004,STRAND=1,ExAC_SAS_MAF=A:0.003311,EA_MAF=A:0.0005,Allele=A,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=676,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000585561.1:c.*410G>A,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000585561	VCF	3_prime_UTR_variant	676	676	0.0	.	.	AC_Male=1;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-124;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=8.95191e-06;AN_POPMAX=111708;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.71429e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.41835e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:0.002586,ExAC_MAF=A:0.0022,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.003117,FLAGS=cds_start_NF,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0001156,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0004,STRAND=1,ExAC_SAS_MAF=A:0.003311,EA_MAF=A:0.0005,Allele=T,IMPACT=MODIFIER,EXON=6/7,ExAC_AMR_MAF=A:9.61e-05,cDNA_position=676,ExAC_NFE_MAF=A:0.01467,SYMBOL=NMT1,Existing_variation=rs146345914,SAS_MAF=A:0.002,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:2.586e-03,HGVSc=ENST00000585561.1:c.*410G>T,ExAC_Adj_MAF=A:0.0002592
CDS|ENST00000585561	VCF	3_prime_UTR_variant	677	677	0.0	.	.	AC_Male=1;AF_NFE=8.95175e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-146;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06078e-06;Hom=0;AF_POPMAX=8.95175e-06;AN_POPMAX=111710;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41279e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.64198e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=162;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.16858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=A,IMPACT=MODIFIER,EXON=6/7,cDNA_position=677,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*411G>A
CDS|ENST00000585561	VCF	3_prime_UTR_variant	678	678	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-92;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06081e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=74;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=6/7,cDNA_position=678,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*412A>C
CDS|ENST00000585561	VCF	3_prime_UTR_variant	698	698	0.0	.	.	AC_Male=0;AF_NFE=8.96282e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-295;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06345e-06;Hom=0;AF_POPMAX=8.96282e-06;AN_POPMAX=111572;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51327e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=226;AF_Female=8.98763e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:8.243e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.5e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=T:0,cDNA_position=698,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764148755,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000585561.1:c.*432C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	699	699	0.0	.	.	AC_Male=35;AF_NFE=1.07544e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|9|11|10|12|4|2|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-103;AF_OTH=1.82415e-04;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=49;Hom_NFE=0;AF=1.99100e-04;Hom=0;AF_POPMAX=2.23441e-03;AN_POPMAX=9846;AC_NFE=12;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|0|4|3|1|2|1|6|7|4|4|0|2|1;AF_Male=2.59586e-04;AF_AFR=0.00000e+00;AC_raw=49;AB_MEDIAN=4.65116e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=2.23441e-03;DP_MEDIAN=74;AF_Female=1.25811e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|49;Hom_raw=0;AF_SAS=3.89838e-04;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=14;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=12;POPMAX=ASJ;AC_POPMAX=22;AC_AFR=0;Hom_SAS=0;AC_ASJ=22;AF_raw=1.98967e-04;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=A:0.0002225,ExAC_MAF=A:0.0002,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0002699,AFR_MAF=A:0.0005453,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=A:0,cDNA_position=699,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs150418753&COSM4067023,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:2.224e-04,HGVSc=ENST00000585561.1:c.*433G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	706	706	0.0	.	.	AC_Male=4;AF_NFE=5.37577e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|2|2|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00079e-202;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.43754e-05;Hom=0;AF_POPMAX=5.37577e-05;AN_POPMAX=111612;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|1;AF_Male=2.96630e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=5.20944e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=152;AF_Female=1.79691e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.35748e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.43633e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,PHENO=0&1,ExAC_EAS_MAF=T:2.472e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.497e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=T:0,cDNA_position=706,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs757227703&COSM4130155,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:2.471e-05,HGVSc=ENST00000585561.1:c.*440C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	707	707	0.0	.	.	AC_Male=5;AF_NFE=1.25390e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|1|2|3|9|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-94;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=17;Hom_NFE=0;AF=6.90524e-05;Hom=0;AF_POPMAX=1.25390e-04;AN_POPMAX=111652;AC_NFE=14;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|0|0|1|1|1|2|0|2|2|0|1|0|1|0|0;AF_Male=3.70749e-05;AF_AFR=0.00000e+00;AC_raw=17;AB_MEDIAN=5.09033e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=64;AF_Female=1.07790e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|17;Hom_raw=0;AF_SAS=9.74596e-05;AS_RF=9.36765e-01;Hom_AMR=0;AC_EAS=0;AC_Female=12;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=3;POPMAX=NFE;AC_POPMAX=14;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=6.90294e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:5.768e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:7.495e-05,AFR_MAF=A:0.0001211,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=A:0,cDNA_position=707,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs781499966,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:5.765e-05,HGVSc=ENST00000585561.1:c.*441G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	712	712	0.0	.	.	AC_Male=1;AF_NFE=3.58230e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-225;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62467e-05;Hom=0;AF_POPMAX=3.58230e-05;AN_POPMAX=111660;AC_NFE=4;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0;AF_Male=7.41499e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.55048e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=196;AF_Female=2.69440e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:3.296e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:5.996e-05,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=T:0,cDNA_position=712,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs746041079,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:3.295e-05,HGVSc=ENST00000585561.1:c.*446G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	713	713	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-212;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06141e-06;Hom=0;AF_POPMAX=2.97779e-05;AN_POPMAX=33582;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.11392e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=158;AF_Female=8.98134e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.08869e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.239e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=G:0,cDNA_position=713,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs756018179,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.*447C>G,ExAC_Adj_MAF=G:8.639e-05
CDS|ENST00000585561	VCF	3_prime_UTR_variant	717	717	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|1|2|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-130;AF_OTH=1.82282e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.03062e-05;Hom=0;AF_POPMAX=2.31911e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|1|1|0|0|0|0;AF_Male=1.48278e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=76;AF_Female=2.69426e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.39678e-01;Hom_AMR=0;AC_EAS=4;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=2.31911e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.03028e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,Allele=T,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=A:0&T:0,cDNA_position=717,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000585561.1:c.*451C>T,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	717	717	0.0	.	.	AC_Male=1;AF_NFE=8.95415e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-239;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21837e-05;Hom=0;AF_POPMAX=5.95557e-05;AN_POPMAX=33582;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=5.31915e-01;Hom_EAS=0;AC_AMR=2;AF_ASJ=0.00000e+00;DP_MEDIAN=153;AF_Female=1.79617e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.48089e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=5.95557e-05;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.238e-06&T:8.238e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0&T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0&T:0.0001156,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0&T:0,Allele=A,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=A:0&T:0,cDNA_position=717,ExAC_NFE_MAF=A:0&T:0,SYMBOL=NMT1,Existing_variation=rs779975972,VARIANT_CLASS=SNV,ExAC_AFR_MAF=A:8.236e-06&T:8.236e-06,HGVSc=ENST00000585561.1:c.*451C>A,ExAC_Adj_MAF=A:8.639e-05&T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	733	733	0.0	.	.	AC_Male=1;AF_NFE=1.79045e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-65;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12163e-06;Hom=0;AF_POPMAX=1.79045e-05;AN_POPMAX=111704;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0;AF_Male=7.41290e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.08500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=57;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.42948e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=A:0,cDNA_position=733,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs768715452,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*467G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	743	743	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-238;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41268e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.42254e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=142;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.49406e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=C:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.499e-05,AFR_MAF=C:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=C:0,cDNA_position=743,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs774095582,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000585561.1:c.*477G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	745	745	0.0	.	.	AC_Male=9;AF_NFE=2.32741e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|11|10|1|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.92447e-104;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=26;Hom_NFE=0;AF=1.05578e-04;Hom=0;AF_POPMAX=2.32741e-04;AN_POPMAX=111712;AC_NFE=26;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|1|3|0|2|5|0|2;AF_Male=6.67141e-05;AF_AFR=0.00000e+00;AC_raw=26;AB_MEDIAN=4.45780e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=98;AF_Female=1.52658e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|26;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=17;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=26;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.05574e-04;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:9.885e-05,ExAC_MAF=T:0.0003,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0.0001798,AFR_MAF=T:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=T:0,cDNA_position=745,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs199671891,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:9.884e-05,HGVSc=ENST00000585561.1:c.*479C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	752	752	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-102;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06075e-06;Hom=0;AF_POPMAX=3.24865e-05;AN_POPMAX=30782;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.59375e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.98021e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24865e-05;AS_RF=7.94592e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=T,IMPACT=MODIFIER,EXON=7/7,cDNA_position=752,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*486C>T
CDS|ENST00000585561	VCF	3_prime_UTR_variant	753	753	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|2|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-67;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21820e-05;Hom=0;AF_POPMAX=1.01523e-04;AN_POPMAX=9850;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.62963e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=1.01523e-04;DP_MEDIAN=51;AF_Female=1.79601e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53178e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=ASJ;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=1;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=2.97779e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.498e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=A:0,cDNA_position=753,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs771441667,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*487G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	754	754	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-154;AF_OTH=1.82282e-04;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06065e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.60938e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=128;AF_Female=8.97989e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=7/7,cDNA_position=754,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*488G>C
CDS|ENST00000585561	VCF	3_prime_UTR_variant	775	775	0.0	.	.	AC_Male=2;AF_NFE=8.95191e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21823e-05;Hom=0;AF_POPMAX=6.49730e-05;AN_POPMAX=30782;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=1.48249e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.91803e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=6.49730e-05;AS_RF=9.01565e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=T:1.647e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.498e-05,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=T:0,cDNA_position=775,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs772957252,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000585561.1:c.*509C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	781	781	0.0	.	.	AC_Male=1;AF_NFE=8.95159e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-165;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95159e-06;AN_POPMAX=111712;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.56897e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=116;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.17542e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.237e-06,ExAC_MAF=G:0.0001,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=G:0,cDNA_position=781,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs375089291,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.*515C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	784	784	0.0	.	.	AC_Male=1;AF_NFE=8.95143e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-140;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06072e-06;Hom=0;AF_POPMAX=8.95143e-06;AN_POPMAX=111714;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41257e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.49153e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=118;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=G:0,cDNA_position=784,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs770200317,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.*518A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	795	795	0.0	.	.	AC_Male=1;AF_NFE=1.79054e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-248;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.12196e-06;Hom=0;AF_POPMAX=1.79054e-05;AN_POPMAX=111698;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41312e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.99184e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=192;AF_Female=8.98069e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.47173e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:1.647e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.997e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=G:0,cDNA_position=795,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs775829411,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000585561.1:c.*529A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	801	801	0.0	.	.	AC_Male=0;AF_NFE=8.95399e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-226;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06124e-06;Hom=0;AF_POPMAX=8.95399e-06;AN_POPMAX=111682;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.30168e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=179;AF_Female=8.98150e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.22854e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.498e-05,AFR_MAF=G:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=G:0,cDNA_position=801,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs763238851,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000585561.1:c.*535A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	3_prime_UTR_variant	802	802	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-84;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06138e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.41389e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.92754e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=69;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.86417e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466777,UNIPARC=UPI0002841053,Consequence=3_prime_UTR_variant&NMD_transcript_variant,Feature=ENST00000585561,STRAND=1,BIOTYPE=nonsense_mediated_decay,Allele=C,IMPACT=MODIFIER,EXON=7/7,cDNA_position=802,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_start_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000585561.1:c.*536T>C
CDS|ENST00000585561	VCF	3_prime_UTR_variant	807	807	0.0	.	.	AC_Male=0;AF_NFE=8.95592e-06;Hom_FIN=0;GQ_MEDIAN=19;AB_HIST_ALT=0|0|1|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.24327e-02;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06167e-06;Hom=0;AF_POPMAX=8.95592e-06;AN_POPMAX=111658;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=2.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=8.98198e-06;GQ_HIST_ALT=0|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.79803e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.237e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.499e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=7/7,ExAC_AMR_MAF=A:0,cDNA_position=807,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs764674925,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*541C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	inframe_deletion	117	120	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|3|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99054e-19;AF_OTH=0.00000e+00;alleles=TACA%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.63922e-05;Hom=0;AF_POPMAX=2.63817e-04;AN_POPMAX=15162;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24225e-05;AF_AFR=2.63817e-04;AC_raw=4;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.07243e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.21158e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=4;AC_AFR=4;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=-:3.614e-05,ExAC_MAF=-:0,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=-:0,AFR_MAF=-:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,HGVS_OFFSET=2,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=-:0,ENSP=ENSP00000466777,Consequence=inframe_deletion&NMD_transcript_variant,Amino_acids=YN/Y,HGVSp=ENSP00000466777.1:p.Asn41del,STRAND=1,ExAC_SAS_MAF=-:0,EA_MAF=-:0.0007,Allele=-,IMPACT=MODERATE,EXON=1/7,ExAC_AMR_MAF=-:0.0004244,cDNA_position=118-120,CDS_position=119-121,ExAC_NFE_MAF=-:0,SYMBOL=NMT1,Existing_variation=rs766213031,VARIANT_CLASS=deletion,Protein_position=40-41,Codons=tACAac/tac,MINIMISED=1,ExAC_AFR_MAF=-:3.295e-05,HGVSc=ENST00000585561.1:c.120_122delAAC,ExAC_Adj_MAF=-:0
CDS|ENST00000585561	VCF	splice_region_variant	125	125	0.0	.	.	AC_Male=4;AF_NFE=2.73010e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25597e-29;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.64955e-05;Hom=0;AF_POPMAX=6.65513e-05;AN_POPMAX=15026;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=3.00680e-05;AF_AFR=6.65513e-05;AC_raw=4;AB_MEDIAN=5.27778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.27137e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62425e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:9.22e-06,ExAC_MAF=C:0.0001,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.668e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=splice_region_variant&synonymous_variant&NMD_transcript_variant,Amino_acids=R,HGVSp=ENST00000585561.1:c.125G>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=C:0,Allele=A,IMPACT=LOW,EXON=1/7,ExAC_AMR_MAF=A:0,cDNA_position=125,CDS_position=126,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs143955814,VARIANT_CLASS=SNV,Protein_position=42,Codons=cgG/cgA,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.125G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	splice_region_variant	335	335	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-33;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.41163e-06;Hom=0;AF_POPMAX=6.76636e-05;AN_POPMAX=29558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.53130e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.32389e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.76636e-05;AS_RF=8.96351e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12123e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=G:1.681e-05,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.000128,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466777,Consequence=splice_region_variant&3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=LOW,EXON=4/7,ExAC_AMR_MAF=G:0,cDNA_position=335,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767459577,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000585561.1:c.*69A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000585561	VCF	splice_region_variant	481	481	0.0	.	.	AC_Male=1;AF_NFE=8.98699e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.49763e-52;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13974e-06;Hom=0;AF_POPMAX=2.97992e-05;AN_POPMAX=33558;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43030e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.59152e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.29846e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.318e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_start_NF,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=splice_region_variant&3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0,Allele=T,IMPACT=LOW,EXON=5/7,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=481,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*215C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	splice_region_variant	481	481	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=60;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.13501e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06987e-06;Hom=0;AF_POPMAX=6.53766e-05;AN_POPMAX=15296;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53766e-05;AC_raw=2;AB_MEDIAN=3.53758e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.07429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.318e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_start_NF,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=splice_region_variant&3_prime_UTR_variant&NMD_transcript_variant,GMAF=A:0.0002,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=5/7,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=481,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,AA_MAF=A:0,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*215C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000585561	VCF	splice_region_variant	596	596	0.0	.	.	AC_Male=1;AF_NFE=2.69624e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-79;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22082e-05;Hom=0;AF_POPMAX=2.69624e-05;AN_POPMAX=111266;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43075e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.43709e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=51;AF_Female=1.79921e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.30930e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841053,ExAC_EAS_MAF=A:8.27e-06,Feature=ENST00000585561,BIOTYPE=nonsense_mediated_decay,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.504e-05,AFR_MAF=A:0,FLAGS=cds_start_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466777,Consequence=splice_region_variant&3_prime_UTR_variant&NMD_transcript_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=5/7,ExAC_AMR_MAF=A:0,cDNA_position=596,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs773364852,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000585561.1:c.*330G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	synonymous_variant	350	350	0.0	.	.	AC_Male=0;AF_NFE=9.11594e-06;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15014e-06;Hom=0;AF_POPMAX=9.11594e-06;AN_POPMAX=109698;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.77778e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=16;AF_Female=9.19912e-06;GQ_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.62962e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=C:8.372e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=C:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.518e-05,AFR_MAF=C:0,FLAGS=cds_end_NF,EAS_MAF=C:0,EUR_MAF=C:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,GMAF=C:0.0002,Amino_acids=S,HGVSp=ENST00000592654.1:c.9T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=LOW,EXON=3/4,ExAC_AMR_MAF=C:0,cDNA_position=350,CDS_position=9,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs200633656,SAS_MAF=C:0.001,VARIANT_CLASS=SNV,Protein_position=3,AA_MAF=C:0,Codons=tcT/tcC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592654.1:c.9T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592654	VCF	synonymous_variant	374	374	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|2|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.22868e-05;Hom=0;AF_POPMAX=9.08045e-05;AN_POPMAX=33038;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.46949e-06;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=6.81818e-01;Hom_EAS=0;AC_AMR=3;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.81347e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.72461e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=9.08045e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=E,HGVSp=ENST00000592654.1:c.33A>G(p.%253D),STRAND=1,Allele=G,IMPACT=LOW,EXON=3/4,cDNA_position=374,CDS_position=33,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=11,Codons=gaA/gaG,MINIMISED=1,HGVSc=ENST00000592654.1:c.33A>G
CDS|ENST00000592654	VCF	synonymous_variant	389	389	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-142;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07917e-06;Hom=0;AF_POPMAX=6.55996e-05;AN_POPMAX=15244;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0;AF_Male=0.00000e+00;AF_AFR=6.55996e-05;AC_raw=1;AB_MEDIAN=4.83146e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.02657e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.95139e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=C:8.272e-06,TREMBL=K7EN82,ExAC_MAF=C:0,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,AFR_MAF=C:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=I,HGVSp=ENST00000592654.1:c.48T>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,EA_MAF=C:0.0002,Allele=C,IMPACT=LOW,EXON=3/4,ExAC_AMR_MAF=C:9.641e-05,cDNA_position=389,CDS_position=48,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs372318247,VARIANT_CLASS=SNV,Protein_position=16,Codons=atT/atC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592654.1:c.48T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592654	VCF	synonymous_variant	395	395	0.0	.	.	AC_Male=1;AF_NFE=8.97747e-06;Hom_FIN=0;GQ_MEDIAN=73;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=9.97611e-06;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.14538e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43307e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.54779e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=89;AF_Female=9.00868e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.44770e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.266e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.504e-05,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=L,HGVSp=ENST00000592654.1:c.54G>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=3/4,ExAC_AMR_MAF=T:0,cDNA_position=395,CDS_position=54,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs754577624,VARIANT_CLASS=SNV,Protein_position=18,Codons=ctG/ctT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.54G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	synonymous_variant	401	401	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07193e-06;Hom=0;AF_POPMAX=3.25457e-05;AN_POPMAX=30726;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43141e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.64286e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25457e-05;AS_RF=8.52320e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592654.1:c.60A>G(p.%253D),STRAND=1,Allele=G,IMPACT=LOW,EXON=3/4,cDNA_position=401,CDS_position=60,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=20,Codons=tcA/tcG,MINIMISED=1,HGVSc=ENST00000592654.1:c.60A>G
CDS|ENST00000592654	VCF	synonymous_variant	413	413	0.0	.	.	AC_Male=1;AF_NFE=8.99006e-06;Hom_FIN=0;GQ_MEDIAN=34;AB_HIST_ALT=0|0|0|0|4|3|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=3;DREF_MEDIAN=4.08532e-04;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=1.35404e-04;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.44760e-05;Hom=0;AF_POPMAX=1.35404e-04;AN_POPMAX=22156;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|0|1|2|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.44114e-06;AF_AFR=1.31406e-04;AC_raw=8;AB_MEDIAN=2.47642e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=4.51467e-05;GQ_HIST_ALT=0|1|1|0|0|1|1|1|0|0|1|0|1|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.54316e-03;Hom_AMR=0;AC_EAS=0;AC_Female=5;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=3;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=C:6.621e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:6.02e-05,AFR_MAF=C:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592654.1:c.72A>C(p.%253D),STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=LOW,EXON=3/4,ExAC_AMR_MAF=C:0.0002899,cDNA_position=413,CDS_position=72,ExAC_NFE_MAF=C:0.0001537,SYMBOL=NMT1,Existing_variation=rs746348189,VARIANT_CLASS=SNV,Protein_position=24,Codons=ggA/ggC,MINIMISED=1,ExAC_AFR_MAF=C:9.060e-05,HGVSc=ENST00000592654.1:c.72A>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592654	VCF	synonymous_variant	419	419	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07701e-06;Hom=0;AF_POPMAX=3.25945e-05;AN_POPMAX=30680;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.66667e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=15;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25945e-05;AS_RF=8.53172e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592654.1:c.78C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/4,cDNA_position=419,CDS_position=78,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=26,Codons=gcC/gcT,MINIMISED=1,HGVSc=ENST00000592654.1:c.78C>T
CDS|ENST00000592654	VCF	synonymous_variant	437	437	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-42;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07501e-06;Hom=0;AF_POPMAX=2.99419e-05;AN_POPMAX=33398;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43450e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.92593e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=27;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.81783e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99419e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=A,HGVSp=ENST00000592654.1:c.96T>C(p.%253D),STRAND=1,Allele=C,IMPACT=LOW,EXON=3/4,cDNA_position=437,CDS_position=96,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=32,Codons=gcT/gcC,MINIMISED=1,HGVSc=ENST00000592654.1:c.96T>C
CDS|ENST00000592654	VCF	synonymous_variant	440	440	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07465e-06;Hom=0;AF_POPMAX=2.99455e-05;AN_POPMAX=33394;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.67568e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=37;AF_Female=9.01518e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.92008e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=2.99455e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=S,HGVSp=ENST00000592654.1:c.99C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/4,cDNA_position=440,CDS_position=99,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=33,Codons=agC/agT,MINIMISED=1,HGVSc=ENST00000592654.1:c.99C>T
CDS|ENST00000592654	VCF	synonymous_variant	458	458	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=25;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15231e-03;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=0;Hom_NFE=0;AF=0.00000e+00;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=RF|AC0;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.50000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=8;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66799e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=F,HGVSp=ENST00000592654.1:c.117C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/4,cDNA_position=458,CDS_position=117,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=39,Codons=ttC/ttT,MINIMISED=1,HGVSc=ENST00000592654.1:c.117C>T
CDS|ENST00000592654	VCF	synonymous_variant	467	467	0.0	.	.	AC_Male=0;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-30;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.78261e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=9.08364e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.39564e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592654.1:c.126G>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=3/4,cDNA_position=467,CDS_position=126,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=42,Codons=acG/acT,HGVSc=ENST00000592654.1:c.126G>T
CDS|ENST00000592654	VCF	synonymous_variant	467	467	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|1|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.69441e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10411e-06;Hom=0;AF_POPMAX=3.02810e-05;AN_POPMAX=33024;AC_NFE=0;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|3|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48671e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=1.60256e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|2|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.95538e-03;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62423e-05;Hom_Female=0;AF_AMR=3.02810e-05;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592654.1:c.126G>A(p.%253D),STRAND=1,Allele=A,IMPACT=LOW,EXON=3/4,cDNA_position=467,CDS_position=126,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=42,Codons=acG/acA,HGVSc=ENST00000592654.1:c.126G>A
CDS|ENST00000592654	VCF	synonymous_variant	473	473	0.0	.	.	AC_Male=13;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|3|2|0|5|2|0|3|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.58518e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=15;Hom_NFE=0;AF=6.19001e-05;Hom=0;AF_POPMAX=4.28788e-04;AN_POPMAX=30318;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|4|2|1|1|1|0|1|0|0|2|1|0|0|1|0|0;AF_Male=9.78076e-05;AF_AFR=6.60153e-05;AC_raw=15;AB_MEDIAN=4.72797e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=1.82795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|15;Hom_raw=0;AF_SAS=4.28788e-04;AS_RF=9.33794e-01;Hom_AMR=0;AC_EAS=1;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.89692e-05;AC_SAS=13;POPMAX=SAS;AC_POPMAX=13;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09088e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.385e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0.0005311,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001156,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592654.1:c.132C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=3/4,ExAC_AMR_MAF=T:9.632e-05,cDNA_position=473,CDS_position=132,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs774578466,VARIANT_CLASS=SNV,Protein_position=44,Codons=ccC/ccT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-05,HGVSc=ENST00000592654.1:c.132C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	synonymous_variant	479	479	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-31;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13839e-06;Hom=0;AF_POPMAX=3.31279e-05;AN_POPMAX=30186;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.54523e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.58333e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.31279e-05;AS_RF=8.33412e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:8.422e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592654.1:c.138C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=LOW,EXON=3/4,ExAC_AMR_MAF=G:0,cDNA_position=479,CDS_position=138,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767261647,VARIANT_CLASS=SNV,Protein_position=46,Codons=ccC/ccG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592654.1:c.138C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	synonymous_variant	500	500	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-42;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06669e-06;Hom=0;AF_POPMAX=3.24971e-05;AN_POPMAX=30772;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42501e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=35;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24971e-05;AS_RF=9.28048e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.289e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=N,HGVSp=ENST00000592654.1:c.159C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=4/4,ExAC_AMR_MAF=T:0,cDNA_position=500,CDS_position=159,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs760391896,VARIANT_CLASS=SNV,Protein_position=53,Codons=aaC/aaT,MINIMISED=1,ExAC_AFR_MAF=T:8.237e-06,HGVSc=ENST00000592654.1:c.159C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	synonymous_variant	503	503	0.0	.	.	AC_Male=1;AF_NFE=8.97054e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-32;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06544e-06;Hom=0;AF_POPMAX=8.97054e-06;AN_POPMAX=111476;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42225e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.48276e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.93308e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:8.285e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.508e-05,AFR_MAF=A:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=T,HGVSp=ENST00000592654.1:c.162C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=4/4,ExAC_AMR_MAF=A:0,cDNA_position=503,CDS_position=162,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs766241230,VARIANT_CLASS=SNV,Protein_position=54,Codons=acC/acA,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592654.1:c.162C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	synonymous_variant	509	509	0.0	.	.	AC_Male=0;AF_NFE=8.97022e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-93;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06521e-06;Hom=0;AF_POPMAX=8.97022e-06;AN_POPMAX=111480;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.90164e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=61;AF_Female=8.98779e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40909e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=G,HGVSp=ENST00000592654.1:c.168C>T(p.%253D),STRAND=1,Allele=T,IMPACT=LOW,EXON=4/4,cDNA_position=509,CDS_position=168,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=56,Codons=ggC/ggT,MINIMISED=1,HGVSc=ENST00000592654.1:c.168C>T
CDS|ENST00000592654	VCF	synonymous_variant	512	512	0.0	.	.	AC_Male=22;AF_NFE=2.68986e-04;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|3|9|6|8|6|4|1|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=1.00000e-61;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=4.48672e-05;AC_OTH=0;Hom_Male=0;AC=37;Hom_NFE=0;AF=1.50378e-04;Hom=0;AF_POPMAX=2.68986e-04;AN_POPMAX=111530;AC_NFE=30;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|6|3|4|4|5|5|3|2|0|2|3|0|0|0|0;AF_Male=1.63236e-04;AF_AFR=0.00000e+00;AC_raw=37;AB_MEDIAN=5.00000e-01;Hom_EAS=0;AC_AMR=6;AF_ASJ=0.00000e+00;DP_MEDIAN=45;AF_Female=1.34805e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|37;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=30;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.50240e-04;Hom_Female=0;AF_AMR=1.78710e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,TREMBL=K7EN82,ExAC_MAF=G:0.0003,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592654.1:c.171C>G(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&G:0,EA_MAF=G:0.0002,Allele=G,IMPACT=LOW,EXON=4/4,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=512,CDS_position=171,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,Protein_position=57,Codons=ccC/ccG,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000592654.1:c.171C>G,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000592654	VCF	synonymous_variant	512	512	0.0	.	.	AC_Male=4;AF_NFE=2.68986e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|2|3|1|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25595e-59;AF_OTH=3.64830e-04;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=2;Hom_Male=0;AC=8;Hom_NFE=0;AF=3.25142e-05;Hom=0;AF_POPMAX=1.30702e-04;AN_POPMAX=15302;AC_NFE=3;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|2|1|1|2|2|0|0|0|0|0|0|0|0|0;AF_Male=2.96793e-05;AF_AFR=1.30702e-04;AC_raw=8;AB_MEDIAN=4.75384e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=43;AF_Female=3.59479e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|8;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.36054e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=AFR;AC_POPMAX=2;AC_AFR=2;Hom_SAS=0;AC_ASJ=0;AF_raw=3.24844e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:4.137e-05&G:0.0001489,TREMBL=K7EN82,ExAC_MAF=G:0.0003,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:4.518e-05&G:0.000241,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=P,HGVSp=ENST00000592654.1:c.171C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0&G:0,EA_MAF=G:0.0002,Allele=T,IMPACT=LOW,EXON=4/4,ExAC_AMR_MAF=T:9.647e-05&G:9.647e-05,cDNA_position=512,CDS_position=171,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs147841016,VARIANT_CLASS=SNV,Protein_position=57,Codons=ccC/ccT,ExAC_AFR_MAF=T:4.118e-05&G:1.483e-04,HGVSc=ENST00000592654.1:c.171C>T,ExAC_Adj_MAF=T:0&G:8.672e-05
CDS|ENST00000592654	VCF	synonymous_variant	524	524	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-74;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06329e-06;Hom=0;AF_POPMAX=5.79845e-05;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53191e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.50090e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79845e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.261e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=T:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_end_NF,EAS_MAF=T:0,EUR_MAF=T:0.001,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0.0001157,ENSP=ENSP00000466827,Consequence=synonymous_variant,GMAF=T:0.0002,Amino_acids=D,HGVSp=ENST00000592654.1:c.183C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=LOW,EXON=4/4,ExAC_AMR_MAF=T:0,cDNA_position=524,CDS_position=183,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs535242567,SAS_MAF=T:0,VARIANT_CLASS=SNV,Protein_position=61,AA_MAF=T:0,Codons=gaC/gaT,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.183C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	synonymous_variant	527	527	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-50;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06339e-06;Hom=0;AF_POPMAX=5.79777e-05;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41851e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.00000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.43104e-01;Hom_AMR=0;AC_EAS=1;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=5.79777e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=synonymous_variant,Amino_acids=K,HGVSp=ENST00000592654.1:c.186G>A(p.%253D),STRAND=1,Allele=A,IMPACT=LOW,EXON=4/4,cDNA_position=527,CDS_position=186,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=62,Codons=aaG/aaA,MINIMISED=1,HGVSc=ENST00000592654.1:c.186G>A
CDS|ENST00000592654	VCF	start_lost	342	342	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-33;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.41163e-06;Hom=0;AF_POPMAX=6.76636e-05;AN_POPMAX=29558;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.53130e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.32389e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=6.76636e-05;AS_RF=8.96351e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=2;POPMAX=SAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12123e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.3),UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:1.681e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0.000128,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=start_lost&splice_region_variant,Amino_acids=M/V,HGVSp=ENSP00000466827.1:p.Met1?,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=HIGH,EXON=3/4,ExAC_AMR_MAF=G:0,cDNA_position=342,CDS_position=1,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs767459577,VARIANT_CLASS=SNV,Protein_position=1,Codons=Atg/Gtg,MINIMISED=1,ExAC_AFR_MAF=G:1.647e-05,HGVSc=ENST00000592654.1:c.1A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	missense_variant	346	346	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51591e-22;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.09459e-05;AN_POPMAX=16408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.23913e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=20;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.20091e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=6.09459e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.07),UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.391e-06,TREMBL=K7EN82,ExAC_MAF=T:0,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=N/T,HGVSp=ENSP00000466827.1:p.Asn2Thr,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=C,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=346,CDS_position=5,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=2,Codons=aAc/aCc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.5A>C,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	346	346	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-62;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.20348e-06;Hom=0;AF_POPMAX=6.67646e-05;AN_POPMAX=14978;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.67646e-05;AC_raw=1;AB_MEDIAN=3.09859e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=71;AF_Female=9.32888e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.02337e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06062e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0.01),UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.391e-06,TREMBL=K7EN82,ExAC_MAF=T:0,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.028),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=N/I,HGVSp=ENSP00000466827.1:p.Asn2Ile,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0.0002,Allele=T,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=T:9.692e-05,cDNA_position=346,CDS_position=5,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs367954716,VARIANT_CLASS=SNV,Protein_position=2,Codons=aAc/aTc,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.5A>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	368	368	0.0	.	.	AC_Male=1;AF_NFE=9.04977e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-52;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10988e-06;Hom=0;AF_POPMAX=9.04977e-06;AN_POPMAX=110500;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.49524e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.10256e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.90362e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:8.312e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.51e-05,AFR_MAF=G:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.004),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=I/M,HGVSp=ENSP00000466827.1:p.Ile9Met,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=G:0,cDNA_position=368,CDS_position=27,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779405921,VARIANT_CLASS=SNV,Protein_position=9,Codons=atC/atG,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-06,HGVSc=ENST00000592654.1:c.27C>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	missense_variant	387	387	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-21;AF_OTH=1.83554e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.08013e-06;Hom=0;AF_POPMAX=.;AN_POPMAX=.;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.70588e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=17;AF_Female=9.03130e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.67445e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=.;AC_POPMAX=.;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.26),UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.002),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=I/V,HGVSp=ENSP00000466827.1:p.Ile16Val,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=3/4,cDNA_position=387,CDS_position=46,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=16,Codons=Att/Gtt,MINIMISED=1,HGVSc=ENST00000592654.1:c.46A>G
CDS|ENST00000592654	VCF	missense_variant	403	403	0.0	.	.	AC_Male=0;AF_NFE=8.97263e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-62;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07163e-06;Hom=0;AF_POPMAX=8.97263e-06;AN_POPMAX=111450;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.37500e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=48;AF_Female=9.00739e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.96701e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.02),UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:8.258e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.129),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=V/E,HGVSp=ENSP00000466827.1:p.Val21Glu,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=A:0,cDNA_position=403,CDS_position=62,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs778561485,VARIANT_CLASS=SNV,Protein_position=21,Codons=gTg/gAg,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592654.1:c.62T>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	missense_variant	405	405	0.0	.	.	AC_Male=0;AF_NFE=8.97167e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-66;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07073e-06;Hom=0;AF_POPMAX=8.97167e-06;AN_POPMAX=111462;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.45455e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=9.00414e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.97942e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.25),UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.258e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=G/C,HGVSp=ENSP00000466827.1:p.Gly22Cys,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=T:0,cDNA_position=405,CDS_position=64,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs747390700,VARIANT_CLASS=SNV,Protein_position=22,Codons=Ggt/Tgt,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.64G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	410	410	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-48;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07186e-06;Hom=0;AF_POPMAX=3.25563e-05;AN_POPMAX=30716;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43097e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.51613e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=31;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25563e-05;AS_RF=9.07079e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.08),UNIPARC=UPI0002841054,ExAC_EAS_MAF=C:8.256e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.015),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=Q/H,HGVSp=ENSP00000466827.1:p.Gln23His,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=C:0,cDNA_position=410,CDS_position=69,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs771371139,VARIANT_CLASS=SNV,Protein_position=23,Codons=caG/caC,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592654.1:c.69G>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592654	VCF	missense_variant	411	411	0.0	.	.	AC_Male=1;AF_NFE=8.97392e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-37;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07279e-06;Hom=0;AF_POPMAX=8.97392e-06;AN_POPMAX=111434;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43152e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=2.97872e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=3.42544e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.09),UNIPARC=UPI0002841054,PHENO=0&1,ExAC_EAS_MAF=A:8.254e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.502e-05,AFR_MAF=A:0,FLAGS=cds_end_NF,EAS_MAF=A:0,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.067),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=missense_variant,GMAF=A:0.0002,Amino_acids=G/R,HGVSp=ENSP00000466827.1:p.Gly24Arg,STRAND=1,ExAC_SAS_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=A:0,cDNA_position=411,CDS_position=70,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs563736659&COSM1493963,SAS_MAF=A:0.001,VARIANT_CLASS=SNV,Protein_position=24,AA_MAF=A:0,Codons=Gga/Aga,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592654.1:c.70G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	missense_variant	427	427	0.0	.	.	AC_Male=1;AF_NFE=8.98053e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-63;AF_OTH=0.00000e+00;alleles=T%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07515e-06;Hom=0;AF_POPMAX=8.98053e-06;AN_POPMAX=111352;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.43528e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.03846e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=52;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.18859e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.37),UNIPARC=UPI0002841054,ExAC_EAS_MAF=C:8.249e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:1.501e-05,AFR_MAF=C:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.005),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=M/T,HGVSp=ENSP00000466827.1:p.Met29Thr,STRAND=1,ExAC_SAS_MAF=C:0,Allele=C,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=C:0,cDNA_position=427,CDS_position=86,ExAC_NFE_MAF=C:0,SYMBOL=NMT1,Existing_variation=rs770043528,VARIANT_CLASS=SNV,Protein_position=29,Codons=aTg/aCg,MINIMISED=1,ExAC_AFR_MAF=C:8.236e-06,HGVSc=ENST00000592654.1:c.86T>C,ExAC_Adj_MAF=C:0
CDS|ENST00000592654	VCF	missense_variant	438	438	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=1;DREF_MEDIAN=7.94328e-56;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=4.48632e-05;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07581e-06;Hom=0;AF_POPMAX=4.48632e-05;AN_POPMAX=22290;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43572e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.25000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.10681e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=FIN;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.36),UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=S/G,HGVSp=ENSP00000466827.1:p.Ser33Gly,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=3/4,cDNA_position=438,CDS_position=97,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=33,Codons=Agc/Ggc,MINIMISED=1,HGVSc=ENST00000592654.1:c.97A>G
CDS|ENST00000592654	VCF	missense_variant	445	445	0.0	.	.	AC_Male=1;AF_NFE=1.79727e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-36;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.15328e-06;Hom=0;AF_POPMAX=1.79727e-05;AN_POPMAX=111280;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=7.43771e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=5.63636e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=9.02120e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.61453e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.04),UNIPARC=UPI0002841054,PHENO=0&1,ExAC_EAS_MAF=T:8.259e-06,TREMBL=K7EN82,ExAC_MAF=T:0.0001,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.502e-05,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.155),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=R/L,HGVSp=ENSP00000466827.1:p.Arg35Leu,STRAND=1,ExAC_SAS_MAF=T:0,EA_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=T:0,cDNA_position=445,CDS_position=104,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs377156745&COSM436718,VARIANT_CLASS=SNV,Protein_position=35,Codons=cGa/cTa,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.104G>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	447	447	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-25;AF_OTH=0.00000e+00;alleles=A%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.07525e-06;Hom=0;AF_POPMAX=3.25839e-05;AN_POPMAX=30690;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43550e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.57143e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.25839e-05;AS_RF=7.10677e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.67),UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.001),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=S/R,HGVSp=ENSP00000466827.1:p.Ser36Arg,STRAND=1,Allele=C,IMPACT=MODERATE,EXON=3/4,cDNA_position=447,CDS_position=106,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=36,Codons=Agc/Cgc,MINIMISED=1,HGVSc=ENST00000592654.1:c.106A>C
CDS|ENST00000592654	VCF	missense_variant	466	466	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=56;AB_HIST_ALT=0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.91433e-02;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.37719e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.02383e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0002841054,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.859),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=T/M,HGVSp=ENSP00000466827.1:p.Thr42Met,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=T,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=T:0,cDNA_position=466,CDS_position=125,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=42,Codons=aCg/aTg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.125C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	466	466	0.0	.	.	AC_Male=1;AF_NFE=9.04634e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-14;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.10479e-06;Hom=0;AF_POPMAX=9.04634e-06;AN_POPMAX=110542;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.48402e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.04348e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=23;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.51858e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,SIFT=deleterious(0),UNIPARC=UPI0002841054,PHENO=0&1,ExAC_EAS_MAF=T:8.343e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.509e-05,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.945),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=T/R,HGVSp=ENSP00000466827.1:p.Thr42Arg,STRAND=1,ExAC_SAS_MAF=T:0,SOMATIC=0&1,Allele=G,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=T:0,cDNA_position=466,CDS_position=125,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs764230766&COSM1679873,VARIANT_CLASS=SNV,Protein_position=42,Codons=aCg/aGg,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.125C>G,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	474	474	0.0	.	.	AC_Male=0;AF_NFE=9.10167e-06;Hom_FIN=0;GQ_MEDIAN=16;AB_HIST_ALT=0|0|0|2|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.45034e-02;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13213e-06;Hom=0;AF_POPMAX=9.10167e-06;AN_POPMAX=109870;AC_NFE=1;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=1.81818e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=12;AF_Female=9.15131e-06;GQ_HIST_ALT=0|0|1|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.57813e-03;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21818e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:8.387e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:1.512e-05,AFR_MAF=A:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.253),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=V/I,HGVSp=ENSP00000466827.1:p.Val45Ile,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=A:0,cDNA_position=474,CDS_position=133,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761622308,VARIANT_CLASS=SNV,Protein_position=45,Codons=Gtc/Atc,MINIMISED=1,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592654.1:c.133G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	missense_variant	481	481	0.0	.	.	AC_Male=5;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|5|2|2|3|0|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58489e-65;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=14;Hom_NFE=0;AF=5.79897e-05;Hom=0;AF_POPMAX=9.23483e-04;AN_POPMAX=15160;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|3|1|1|1|0|0|0|0|1|1|1|2|0|1|0|1|1|1;AF_Male=3.77729e-05;AF_AFR=9.23483e-04;AC_raw=15;AB_MEDIAN=4.44444e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=8.25294e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|14;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.36291e-01;Hom_AMR=0;AC_EAS=0;AC_Female=9;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=14;AC_AFR=14;Hom_SAS=0;AC_ASJ=0;AF_raw=6.09093e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:0.0001096,TREMBL=K7EN82,ExAC_MAF=G:0,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.003),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=K/R,HGVSp=ENSP00000466827.1:p.Lys47Arg,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0.0014,Allele=G,IMPACT=MODERATE,EXON=3/4,ExAC_AMR_MAF=G:0.001254,cDNA_position=481,CDS_position=140,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs144433221,VARIANT_CLASS=SNV,Protein_position=47,Codons=aAg/aGg,MINIMISED=1,ExAC_AFR_MAF=G:1.071e-04,HGVSc=ENST00000592654.1:c.140A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	missense_variant	493	493	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-43;AF_OTH=0.00000e+00;alleles=T%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06782e-06;Hom=0;AF_POPMAX=3.24950e-05;AN_POPMAX=30774;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.42677e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.40426e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24950e-05;AS_RF=7.83979e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06058e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(1),UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=V/E,HGVSp=ENSP00000466827.1:p.Val51Glu,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=4/4,cDNA_position=493,CDS_position=152,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=51,Codons=gTg/gAg,MINIMISED=1,HGVSc=ENST00000592654.1:c.152T>A
CDS|ENST00000592654	VCF	missense_variant	504	504	0.0	.	.	AC_Male=1;AF_NFE=1.79398e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15479e-64;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13028e-06;Hom=0;AF_POPMAX=1.79398e-05;AN_POPMAX=111484;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|2|0|0|0|0|0|0;AF_Male=7.42148e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.25373e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=67;AF_Female=8.98876e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.13408e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12117e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.05),UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:1.657e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:3.015e-05,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.011),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=H/Y,HGVSp=ENSP00000466827.1:p.His55Tyr,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=4/4,ExAC_AMR_MAF=T:0,cDNA_position=504,CDS_position=163,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs753759265,VARIANT_CLASS=SNV,Protein_position=55,Codons=Cat/Tat,MINIMISED=1,ExAC_AFR_MAF=T:1.647e-05,HGVSc=ENST00000592654.1:c.163C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	513	513	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|1|0|0|0|0|1|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25594e-36;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21939e-05;Hom=0;AF_POPMAX=1.15969e-04;AN_POPMAX=17246;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|0|1|0|0|0|1|0|1|0|0|0|0|0|0|0|0;AF_Male=7.42027e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.77324e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=1.79762e-05;GQ_HIST_ALT=0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=3.24907e-05;AS_RF=8.84156e-01;Hom_AMR=0;AC_EAS=2;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.15969e-04;AC_SAS=1;POPMAX=EAS;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:8.272e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.111),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=V/M,HGVSp=ENSP00000466827.1:p.Val58Met,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODERATE,EXON=4/4,ExAC_AMR_MAF=A:0,cDNA_position=513,CDS_position=172,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs752448187,VARIANT_CLASS=SNV,Protein_position=58,Codons=Gtg/Atg,MINIMISED=1,ExAC_AFR_MAF=A:8.237e-06,HGVSc=ENST00000592654.1:c.172G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	missense_variant	519	519	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-75;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06372e-06;Hom=0;AF_POPMAX=3.24886e-05;AN_POPMAX=30780;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.15584e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=77;AF_Female=8.98521e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.24886e-05;AS_RF=9.41661e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.28),UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:8.265e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.025),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=P/S,HGVSp=ENSP00000466827.1:p.Pro60Ser,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODERATE,EXON=4/4,ExAC_AMR_MAF=T:0,cDNA_position=519,CDS_position=178,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs758111913,VARIANT_CLASS=SNV,Protein_position=60,Codons=Cct/Tct,MINIMISED=1,ExAC_AFR_MAF=T:8.236e-06,HGVSc=ENST00000592654.1:c.178C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	missense_variant	520	520	0.0	.	.	AC_Male=0;AF_NFE=8.96363e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-36;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06355e-06;Hom=0;AF_POPMAX=8.96363e-06;AN_POPMAX=111562;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.41176e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=34;AF_Female=8.98505e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00024e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.05),UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.032),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=P/L,HGVSp=ENSP00000466827.1:p.Pro60Leu,STRAND=1,Allele=T,IMPACT=MODERATE,EXON=4/4,cDNA_position=520,CDS_position=179,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=60,Codons=cCt/cTt,MINIMISED=1,HGVSc=ENST00000592654.1:c.179C>T
CDS|ENST00000592654	VCF	missense_variant	522	522	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|1|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-72;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=3;Hom_NFE=0;AF=1.21915e-05;Hom=0;AF_POPMAX=1.73933e-04;AN_POPMAX=17248;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|1|0|0|0|1|0|0|0|0|0|0;AF_Male=1.48381e-05;AF_AFR=0.00000e+00;AC_raw=3;AB_MEDIAN=4.76190e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=8.98586e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|3;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53006e-01;Hom_AMR=0;AC_EAS=3;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=1.73933e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=3;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.21817e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=tolerated(0.16),UNIPARC=UPI0002841054,PHENO=0&1,ExAC_EAS_MAF=A:1.653e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_end_NF,EAS_MAF=A:0,EUR_MAF=A:0.001,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=benign(0.015),SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0.0002313,ENSP=ENSP00000466827,Consequence=missense_variant,GMAF=A:0.0002,Amino_acids=D/N,HGVSp=ENSP00000466827.1:p.Asp61Asn,STRAND=1,ExAC_SAS_MAF=A:0,SOMATIC=0&1,Allele=A,IMPACT=MODERATE,EXON=4/4,ExAC_AMR_MAF=A:0,cDNA_position=522,CDS_position=181,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs201386803&COSM349346,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=61,AA_MAF=A:0,Codons=Gac/Aac,MINIMISED=1,ExAC_AFR_MAF=A:1.647e-05,HGVSc=ENST00000592654.1:c.181G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	missense_variant	543	543	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|1|1|0|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.58114e-54;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.62509e-05;Hom=0;AF_POPMAX=1.19119e-04;AN_POPMAX=33580;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|2|1|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.41697e-06;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=5.40000e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=39;AF_Female=2.69508e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99062e-01;Hom_AMR=0;AC_EAS=0;AC_Female=3;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.62422e-05;Hom_Female=0;AF_AMR=1.19119e-04;CSQ=ALLELE_NUM=1,SIFT=deleterious(0),UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=possibly_damaging(0.736),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=E/K,HGVSp=ENSP00000466827.1:p.Glu68Lys,STRAND=1,Allele=A,IMPACT=MODERATE,EXON=4/4,cDNA_position=543,CDS_position=202,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=68,Codons=Gag/Aag,MINIMISED=1,HGVSc=ENST00000592654.1:c.202G>A
CDS|ENST00000592654	VCF	missense_variant	546	546	0.0	.	.	AC_Male=1;AF_NFE=8.96106e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-53;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06296e-06;Hom=0;AF_POPMAX=8.96106e-06;AN_POPMAX=111594;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=7.41730e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.46809e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=47;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.00924e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.06055e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SIFT=deleterious(0.01),UNIPARC=UPI0002841054,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,FLAGS=cds_end_NF,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,PolyPhen=probably_damaging(0.932),SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,Consequence=missense_variant,Amino_acids=P/A,HGVSp=ENSP00000466827.1:p.Pro69Ala,STRAND=1,Allele=G,IMPACT=MODERATE,EXON=4/4,cDNA_position=546,CDS_position=205,SYMBOL=NMT1,VARIANT_CLASS=SNV,Protein_position=69,Codons=Ccc/Gcc,MINIMISED=1,HGVSc=ENST00000592654.1:c.205C>G
CDS|ENST00000592654	dbSNP	sequence_variant	3	3	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1313864701;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	9	9	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1453127306;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	11	11	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1341980277;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	16	16	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs901932233;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	17	17	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs958893014;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	25	25	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs992789543;alleles=T%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	26	26	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1026746853;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	38	38	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1169359475;alleles=G%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	41	41	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1431663565;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	44	44	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs917262938;alleles=C%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	54	54	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1383642246;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	60	60	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs950726525;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	61	61	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs554503247;alleles=T%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	64	64	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs755246638;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	66	66	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1016546921;alleles=C%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	76	76	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs926053436;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	80	80	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs936169149;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	81	81	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1437814692;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	82	82	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1040289332;alleles=T%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	84	84	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1179390669;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	86	86	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs142583737;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	87	87	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs534812917;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	90	90	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs900057985;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	94	94	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1398912147;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	100	100	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs765363094;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	104	104	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1051336001;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	105	105	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1246168927;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	106	107	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1358020432;alleles=AG%2C-
CDS|ENST00000592654	dbSNP	sequence_variant	115	115	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1277612187;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	117	117	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs553401629;alleles=A%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	119	119	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1350240491;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	120	120	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1309722363;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	121	121	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1411756098;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	123	123	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1363722402;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	135	135	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1302623337;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	138	139	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1406235594;alleles=GT%2C-
CDS|ENST00000592654	dbSNP	sequence_variant	140	140	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1416202927;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	144	144	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs960449146;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	162	162	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs991840054;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	164	164	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1469914298;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	174	174	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs913576423;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	177	177	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs183813794;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	182	182	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1184888640;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	183	183	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1479171451;alleles=T%2C-
CDS|ENST00000592654	dbSNP	sequence_variant	184	184	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs890110734;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	197	197	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1459311619;alleles=A%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	199	199	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1004530344;alleles=C%2CG%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	200	200	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1014666335;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	203	204	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1204363937;alleles=AG%2C-
CDS|ENST00000592654	dbSNP	sequence_variant	206	206	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1351055361;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	207	207	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1290144321;alleles=A%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	209	214	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1221683791;alleles=GAAACT%2C-
CDS|ENST00000592654	dbSNP	sequence_variant	215	215	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1282783829;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	218	218	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1437248151;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	220	220	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs189129818;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	235	235	0.0	+	.	consequence_type=missense_variant;id=rs752810524;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	237	237	0.0	+	.	consequence_type=missense_variant;id=rs758247752;alleles=T%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	238	238	0.0	+	.	consequence_type=missense_variant;id=rs1199096532;alleles=T%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	241	241	0.0	+	.	consequence_type=missense_variant;id=rs1286861992;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	242	242	0.0	+	.	consequence_type=synonymous_variant;id=rs777402320;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	243	243	0.0	+	.	consequence_type=missense_variant;id=rs1192808116;alleles=C%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	244	244	0.0	+	.	consequence_type=missense_variant;id=rs1212522731;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	249	249	0.0	+	.	consequence_type=missense_variant;id=rs140455291;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	250	250	0.0	+	.	consequence_type=missense_variant;id=rs757177482;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	262	262	0.0	+	.	consequence_type=missense_variant;id=rs780748535;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	265	265	0.0	+	.	consequence_type=missense_variant;id=rs774451911;alleles=A%2CG%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	277	277	0.0	+	.	consequence_type=missense_variant;id=rs1468231466;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	282	282	0.0	+	.	consequence_type=missense_variant;id=rs3087878;alleles=C%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	287	287	0.0	+	.	consequence_type=synonymous_variant;id=rs375158125;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	292	292	0.0	+	.	consequence_type=missense_variant;id=rs201559014;alleles=A%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	294	294	0.0	+	.	consequence_type=missense_variant;id=rs779784731;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	302	302	0.0	+	.	consequence_type=synonymous_variant;id=rs141656657;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	304	304	0.0	+	.	consequence_type=missense_variant;id=rs1399730029;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	305	305	0.0	+	.	consequence_type=synonymous_variant;id=rs1315823029;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	311	311	0.0	+	.	consequence_type=synonymous_variant;id=rs369434915;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	321	321	0.0	+	.	consequence_type=missense_variant;id=rs1405046109;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	322	322	0.0	+	.	consequence_type=missense_variant;id=rs1284414737;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	323	323	0.0	+	.	consequence_type=synonymous_variant;id=rs184508172;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	326	326	0.0	+	.	consequence_type=missense_variant;id=rs1231776580;alleles=G%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	330	330	0.0	+	.	consequence_type=missense_variant;id=rs1281614790;alleles=C%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	336	336	0.0	+	.	consequence_type=missense_variant;id=rs761306458;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	342	342	0.0	+	.	consequence_type=start_lost;id=rs767459577;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	346	346	0.0	+	.	consequence_type=missense_variant;id=rs367954716;alleles=A%2CC%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	350	350	0.0	+	.	consequence_type=synonymous_variant;id=rs200633656;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	353	353	0.0	+	.	consequence_type=missense_variant;id=rs1018863986;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	362	362	0.0	+	.	consequence_type=missense_variant;id=rs1051019368;alleles=G%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	368	368	0.0	+	.	consequence_type=missense_variant;id=rs779405921;alleles=C%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	374	374	0.0	+	.	consequence_type=synonymous_variant;id=rs1382805858;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	387	387	0.0	+	.	consequence_type=missense_variant;id=rs1463089836;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	388	388	0.0	+	.	consequence_type=missense_variant;id=rs1308984921;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	389	389	0.0	+	.	consequence_type=synonymous_variant;id=rs372318247;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	395	395	0.0	+	.	consequence_type=synonymous_variant;id=rs754577624;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	401	401	0.0	+	.	consequence_type=synonymous_variant;id=rs1391388443;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	403	403	0.0	+	.	consequence_type=missense_variant;id=rs778561485;alleles=T%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	405	405	0.0	+	.	consequence_type=missense_variant;id=rs747390700;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	409	409	0.0	+	.	consequence_type=missense_variant;id=rs1335366133;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	410	410	0.0	+	.	consequence_type=missense_variant;id=rs771371139;alleles=G%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	411	411	0.0	+	.	consequence_type=missense_variant;id=rs563736659;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	413	413	0.0	+	.	consequence_type=synonymous_variant;id=rs746348189;alleles=A%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	414	414	0.0	+	.	consequence_type=missense_variant;id=rs1294041634;alleles=C%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	415	415	0.0	+	.	consequence_type=missense_variant;id=rs1416691571;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	417	417	0.0	+	.	consequence_type=missense_variant;id=rs868718436;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	419	419	0.0	+	.	consequence_type=synonymous_variant;id=rs1229714849;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	426	426	0.0	+	.	consequence_type=missense_variant;id=rs1348860194;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	427	427	0.0	+	.	consequence_type=missense_variant;id=rs770043528;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	433	433	0.0	+	.	consequence_type=missense_variant;id=rs775419569;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	434	434	0.0	+	.	consequence_type=synonymous_variant;id=rs972147914;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	435	435	0.0	+	.	consequence_type=missense_variant;id=rs1297768336;alleles=G%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	436	436	0.0	+	.	consequence_type=missense_variant;id=rs1443418786;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	437	437	0.0	+	.	consequence_type=synonymous_variant;id=rs1338651806;alleles=T%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	438	438	0.0	+	.	consequence_type=missense_variant;id=rs1196722115;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	440	440	0.0	+	.	consequence_type=synonymous_variant;id=rs1244710451;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	445	445	0.0	+	.	consequence_type=missense_variant;id=rs377156745;alleles=G%2CA%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	447	447	0.0	+	.	consequence_type=missense_variant;id=rs1182546534;alleles=A%2CC
CDS|ENST00000592654	dbSNP	sequence_variant	454	454	0.0	+	.	consequence_type=missense_variant;id=rs1391284036;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	458	458	0.0	+	.	consequence_type=synonymous_variant;id=rs1253657974;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	466	466	0.0	+	.	consequence_type=missense_variant;id=rs764230766;alleles=C%2CG%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	467	467	0.0	+	.	consequence_type=synonymous_variant;id=rs1170526700;alleles=G%2CA%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	473	473	0.0	+	.	consequence_type=synonymous_variant;id=rs774578466;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	474	474	0.0	+	.	consequence_type=missense_variant;id=rs761622308;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	479	479	0.0	+	.	consequence_type=synonymous_variant;id=rs767261647;alleles=C%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	481	481	0.0	+	.	consequence_type=missense_variant;id=rs144433221;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	488	488	0.0	+	.	consequence_type=splice_region_variant;id=rs199678185;alleles=C%2CA%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	493	493	0.0	+	.	consequence_type=missense_variant;id=rs1216003679;alleles=T%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	500	500	0.0	+	.	consequence_type=synonymous_variant;id=rs760391896;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	503	503	0.0	+	.	consequence_type=synonymous_variant;id=rs766241230;alleles=C%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	504	504	0.0	+	.	consequence_type=missense_variant;id=rs753759265;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	509	509	0.0	+	.	consequence_type=synonymous_variant;id=rs1269052802;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	512	512	0.0	+	.	consequence_type=synonymous_variant;id=rs147841016;alleles=C%2CG%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	513	513	0.0	+	.	consequence_type=missense_variant;id=rs752448187;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	518	518	0.0	+	.	consequence_type=synonymous_variant;id=rs1250252141;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	519	519	0.0	+	.	consequence_type=missense_variant;id=rs758111913;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	520	520	0.0	+	.	consequence_type=missense_variant;id=rs1421268751;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	522	522	0.0	+	.	consequence_type=missense_variant;id=rs201386803;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	524	524	0.0	+	.	consequence_type=synonymous_variant;id=rs535242567;alleles=C%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	525	525	0.0	+	.	consequence_type=missense_variant;id=rs986408291;alleles=A%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	527	527	0.0	+	.	consequence_type=synonymous_variant;id=rs1418173661;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	538	538	0.0	+	.	consequence_type=missense_variant;id=rs955288678;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	539	539	0.0	+	.	consequence_type=synonymous_variant;id=rs1456376961;alleles=C%2CG%2CT
CDS|ENST00000592654	dbSNP	sequence_variant	540	540	0.0	+	.	consequence_type=missense_variant;id=rs1161073719;alleles=C%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	543	543	0.0	+	.	consequence_type=missense_variant;id=rs1305018160;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	545	545	0.0	+	.	consequence_type=synonymous_variant;id=rs910463482;alleles=G%2CA
CDS|ENST00000592654	dbSNP	sequence_variant	546	546	0.0	+	.	consequence_type=missense_variant;id=rs1366323829;alleles=C%2CG
CDS|ENST00000592654	dbSNP	sequence_variant	200	201	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1453019660;alleles=-%2CTA
CDS|ENST00000592654	dbSNP	sequence_variant	213	213	0.0	+	.	consequence_type=5_prime_UTR_variant;id=rs1043770124;alleles=C%2CT
CDS|ENST00000592654	VCF	splice_region_variant	488	488	0.0	.	.	AC_Male=1;AF_NFE=8.98699e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.49763e-52;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=8.13974e-06;Hom=0;AF_POPMAX=2.97992e-05;AN_POPMAX=33558;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|1|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.43030e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=4.59152e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.29846e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=2.97992e-05;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:8.318e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_end_NF,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=splice_region_variant&synonymous_variant,GMAF=A:0.0002,Amino_acids=G,HGVSp=ENST00000592654.1:c.147C>T(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=T,IMPACT=LOW,EXON=4/4,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=488,CDS_position=147,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=49,AA_MAF=A:0,Codons=ggC/ggT,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592654.1:c.147C>T,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	splice_region_variant	488	488	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=60;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.13501e-03;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.06987e-06;Hom=0;AF_POPMAX=6.53766e-05;AN_POPMAX=15296;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=6.53766e-05;AC_raw=2;AB_MEDIAN=3.53758e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=8.99896e-06;GQ_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.07429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=8.12110e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:8.318e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=A:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0,AFR_MAF=A:0,FLAGS=cds_end_NF,EAS_MAF=A:0.0014,EUR_MAF=A:0,Feature_type=Transcript,DOMAINS=hmmpanther:PTHR11377&hmmpanther:PTHR11377:SF7&Superfamily_domains:SSF55729,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=splice_region_variant&synonymous_variant,GMAF=A:0.0002,Amino_acids=G,HGVSp=ENST00000592654.1:c.147C>A(p.%253D),STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=LOW,EXON=4/4,ExAC_AMR_MAF=A:9.711e-05,cDNA_position=488,CDS_position=147,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs199678185,SAS_MAF=A:0,VARIANT_CLASS=SNV,Protein_position=49,AA_MAF=A:0,Codons=ggC/ggA,ExAC_AFR_MAF=A:8.236e-06,HGVSc=ENST00000592654.1:c.147C>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	237	237	0.0	.	.	AC_Male=1;AF_NFE=9.20793e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-78;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13846e-06;Hom=0;AF_POPMAX=9.20793e-06;AN_POPMAX=108602;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=7.53477e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.60000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=50;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.26429e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09934e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:8.304e-06,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:1.508e-05,AFR_MAF=G:0,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=G:0,cDNA_position=237,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs758247752,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.237e-06,HGVSc=ENST00000592654.1:c.-105T>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	238	238	0.0	.	.	AC_Male=1;AF_NFE=9.20082e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-91;AF_OTH=0.00000e+00;alleles=T%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.13363e-06;Hom=0;AF_POPMAX=9.20082e-06;AN_POPMAX=108686;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=7.52627e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.53571e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=56;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.83900e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=G,IMPACT=MODIFIER,EXON=2/4,cDNA_position=238,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-104T>G
CDS|ENST00000592654	VCF	5_prime_UTR_variant	241	241	0.0	.	.	AC_Male=1;AF_NFE=9.18628e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.16228e-41;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12361e-06;Hom=0;AF_POPMAX=9.18628e-06;AN_POPMAX=108858;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.50875e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.54545e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=33;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.88840e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09927e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=A,IMPACT=MODIFIER,EXON=2/4,cDNA_position=241,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-101G>A
CDS|ENST00000592654	VCF	5_prime_UTR_variant	242	242	0.0	.	.	AC_Male=148;AF_NFE=1.34979e-03;Hom_FIN=0;GQ_MEDIAN=80;AB_HIST_ALT=0|0|4|13|34|85|90|44|24|6|1|2|0|0|1|0|0|0|0|0;AC_FIN=74;DREF_MEDIAN=1.00000e-08;AF_OTH=1.30939e-03;alleles=T%2CC;AF_FIN=3.42910e-03;AC_OTH=7;Hom_Male=0;AC=275;Hom_NFE=0;AF=1.14690e-03;Hom=0;AF_POPMAX=3.42910e-03;AN_POPMAX=21580;AC_NFE=145;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|5|4|20|31|38|39|37|27|29|22|24|7|6|3|2|2|0|1;AF_Male=1.12191e-03;AF_AFR=1.81476e-03;AC_raw=304;AB_MEDIAN=3.07692e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=1.23127e-03;DP_MEDIAN=42;AF_Female=1.17747e-03;GQ_HIST_ALT=4|4|6|8|5|9|8|12|6|14|13|6|13|13|19|10|18|17|12|107;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=5.26862e-02;Hom_AMR=0;AC_EAS=6;AC_Female=127;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.51206e-04;AC_SAS=0;POPMAX=FIN;AC_POPMAX=74;AC_AFR=27;Hom_SAS=0;AC_ASJ=12;AF_raw=1.24619e-03;Hom_Female=0;AF_AMR=1.20409e-04;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=C:0.001857,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=C:0.001923,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=C:0.001052,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=C:0.005814,Allele=C,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=C:0.001447,cDNA_position=242,ExAC_NFE_MAF=C:0.01002,SYMBOL=NMT1,Existing_variation=rs777402320,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=C:1.911e-03,HGVSc=ENST00000592654.1:c.-100T>C,ExAC_Adj_MAF=C:0.000438
CDS|ENST00000592654	VCF	5_prime_UTR_variant	243	243	0.0	.	.	AC_Male=0;AF_NFE=9.18577e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.98107e-80;AF_OTH=0.00000e+00;alleles=C%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12368e-06;Hom=0;AF_POPMAX=9.18577e-06;AN_POPMAX=108864;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=6.42857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=42;AF_Female=9.14645e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.40367e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09930e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=G,IMPACT=MODIFIER,EXON=2/4,cDNA_position=243,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-99C>G
CDS|ENST00000592654	VCF	5_prime_UTR_variant	249	249	0.0	.	.	AC_Male=6;AF_NFE=4.58573e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|3|2|4|8|1|1|0|1|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30957e-54;AF_OTH=1.83352e-04;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=1;Hom_Male=0;AC=21;Hom_NFE=0;AF=8.63501e-05;Hom=0;AF_POPMAX=9.81804e-04;AN_POPMAX=15278;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|2|2|5|2|2|2|0|3|0|0|1|0|1|0|0|1;AF_Male=4.49384e-05;AF_AFR=9.81804e-04;AC_raw=21;AB_MEDIAN=5.21739e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=36;AF_Female=1.36761e-04;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|21;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.54441e-01;Hom_AMR=0;AC_EAS=0;AC_Female=15;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=15;AC_AFR=15;Hom_SAS=0;AC_ASJ=0;AF_raw=8.60860e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:8.336e-05,TREMBL=K7EN82,ExAC_MAF=G:0,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=G:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:3.034e-05,AFR_MAF=G:0,FLAGS=cds_end_NF,EAS_MAF=G:0,EUR_MAF=G:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,GMAF=G:0.0002,STRAND=1,ExAC_SAS_MAF=G:0,EA_MAF=G:0.0011,Allele=G,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=G:0.000789,cDNA_position=249,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs140455291,SAS_MAF=G:0,VARIANT_CLASS=SNV,AA_MAF=G:0,MINIMISED=1,ExAC_AFR_MAF=G:8.236e-05,HGVSc=ENST00000592654.1:c.-93A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	250	250	0.0	.	.	AC_Male=2;AF_NFE=5.50327e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.29463e-76;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.46765e-05;Hom=0;AF_POPMAX=5.50327e-05;AN_POPMAX=109026;AC_NFE=6;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|1|0|0|1|0|0|0|0|0|0|0|0;AF_Male=1.49817e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.64551e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=99;AF_Female=3.64797e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.53507e-01;Hom_AMR=0;AC_EAS=0;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.45964e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:2.508e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:4.569e-05,AFR_MAF=G:0,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=G:0,cDNA_position=250,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs757177482,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:2.471e-05,HGVSc=ENST00000592654.1:c.-92A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	262	262	0.0	.	.	AC_Male=3;AF_NFE=4.59441e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|2|1|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.25893e-54;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=5;Hom_NFE=0;AF=2.05744e-05;Hom=0;AF_POPMAX=4.59441e-05;AN_POPMAX=108828;AC_NFE=5;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|2|1|0|0|1|0|0|0|0|0|0|0|0|0|0;AF_Male=2.24908e-05;AF_AFR=0.00000e+00;AC_raw=5;AB_MEDIAN=5.80645e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.82428e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|5;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.99531e-01;Hom_AMR=0;AC_EAS=0;AC_Female=2;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=5;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.04965e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:4.372e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:8.027e-05,AFR_MAF=T:0,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=T:0,cDNA_position=262,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs780748535,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=T:4.118e-05,HGVSc=ENST00000592654.1:c.-80C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	265	265	0.0	.	.	AC_Male=6;AF_NFE=6.46365e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|1|1|0|3|0|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-50;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=2.88843e-05;Hom=0;AF_POPMAX=6.46365e-05;AN_POPMAX=108298;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|1|1|0|2|1|1|0|0|0|0|0|1|0|0|0|0;AF_Male=4.50857e-05;AF_AFR=0.00000e+00;AC_raw=7;AB_MEDIAN=4.32432e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=38;AF_Female=9.15198e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.86984e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0&G:0,Allele=G,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=T:0&G:0,cDNA_position=265,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000592654.1:c.-77A>G,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	265	265	0.0	.	.	AC_Male=1;AF_NFE=9.23378e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-64;AF_OTH=0.00000e+00;alleles=A%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.12633e-06;Hom=0;AF_POPMAX=9.23378e-06;AN_POPMAX=108298;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=7.51428e-06;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.22727e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=44;AF_Female=0.00000e+00;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.51003e-01;Hom_AMR=0;AC_EAS=0;AC_Female=0;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.09977e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=2,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:9.437e-06&G:3.775e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:1.748e-05&G:6.991e-05,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0&G:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=T:0&G:0,Allele=T,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=T:0&G:0,cDNA_position=265,ExAC_NFE_MAF=T:0&G:0,SYMBOL=NMT1,Existing_variation=rs774451911,VARIANT_CLASS=SNV,ExAC_AFR_MAF=T:8.238e-06&G:3.295e-05,HGVSc=ENST00000592654.1:c.-77A>T,ExAC_Adj_MAF=T:0&G:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	277	277	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.00000e-24;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.15155e-06;Hom=0;AF_POPMAX=2.99330e-05;AN_POPMAX=33408;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.12500e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=32;AF_Female=9.21302e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=2.89217e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10004e-06;Hom_Female=0;AF_AMR=2.99330e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=G,IMPACT=MODIFIER,EXON=2/4,cDNA_position=277,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-65A>G
CDS|ENST00000592654	VCF	5_prime_UTR_variant	294	294	0.0	.	.	AC_Male=0;AF_NFE=9.88807e-06;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-130;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.33099e-06;Hom=0;AF_POPMAX=9.88807e-06;AN_POPMAX=101132;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=5.14563e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=103;AF_Female=9.61908e-06;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=9.33183e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10129e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:1.315e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:2.529e-05,AFR_MAF=G:0,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=G:0,cDNA_position=294,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs779784731,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=G:8.261e-06,HGVSc=ENST00000592654.1:c.-48A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	302	302	0.0	.	.	AC_Male=2;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|1|1|2|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.10793e-31;AF_OTH=0.00000e+00;alleles=A%2CG;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=6;Hom_NFE=0;AF=2.78394e-05;Hom=0;AF_POPMAX=3.99467e-04;AN_POPMAX=15020;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|1|0|1|2|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.68939e-05;AF_AFR=0.00000e+00;AC_raw=6;AB_MEDIAN=4.91379e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=29;AF_Female=4.11794e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|6;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.74988e-01;Hom_AMR=0;AC_EAS=6;AC_Female=4;Hom_AFR=0;Hom_ASJ=0;AF_EAS=3.99467e-04;AC_SAS=0;POPMAX=EAS;AC_POPMAX=6;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=2.46164e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=G:6.366e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=G:0,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=G:0,AFR_MAF=G:0,FLAGS=cds_end_NF,EAS_MAF=G:0,EUR_MAF=G:0.003,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=G:0.001103,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,GMAF=G:0.0006,STRAND=1,ExAC_SAS_MAF=G:0,Allele=G,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=G:0,cDNA_position=302,ExAC_NFE_MAF=G:0,SYMBOL=NMT1,Existing_variation=rs141656657,SAS_MAF=G:0,VARIANT_CLASS=SNV,AA_MAF=G:0,MINIMISED=1,ExAC_AFR_MAF=G:3.314e-05,HGVSc=ENST00000592654.1:c.-40A>G,ExAC_Adj_MAF=G:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	304	304	0.0	.	.	AC_Male=3;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|2|1|1|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=6.30719e-25;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=4;Hom_NFE=0;AF=1.87099e-05;Hom=0;AF_POPMAX=1.31596e-04;AN_POPMAX=30396;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|1|0|1|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=2.55437e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=4.49730e-01;Hom_EAS=0;AC_AMR=4;AF_ASJ=0.00000e+00;DP_MEDIAN=22;AF_Female=1.03795e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|4;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.66438e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AMR;AC_POPMAX=4;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64119e-05;Hom_Female=0;AF_AMR=1.31596e-04;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=T,IMPACT=MODIFIER,EXON=2/4,cDNA_position=304,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-38G>T
CDS|ENST00000592654	VCF	5_prime_UTR_variant	305	305	0.0	.	.	AC_Male=0;AF_NFE=1.12471e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=2.51189e-23;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=4.76844e-06;Hom=0;AF_POPMAX=1.12471e-05;AN_POPMAX=88912;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.92857e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=28;AF_Female=1.05753e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.93464e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10344e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=T,IMPACT=MODIFIER,EXON=2/4,cDNA_position=305,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-37C>T
CDS|ENST00000592654	VCF	5_prime_UTR_variant	311	311	0.0	.	.	AC_Male=6;AF_NFE=8.41548e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|2|3|1|2|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.15518e-38;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=7;Hom_NFE=0;AF=3.50814e-05;Hom=0;AF_POPMAX=8.41548e-05;AN_POPMAX=83180;AC_NFE=7;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|1|0|1|0|2|1|0|1|1|1|0|0|0|0|0|0|0|0|0;AF_Male=5.48296e-05;AF_AFR=0.00000e+00;AC_raw=8;AB_MEDIAN=4.21637e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=30;AF_Female=1.10980e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|7;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.12023e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=7;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=3.28394e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:5.723e-05,TREMBL=K7EN82,ExAC_MAF=A:0.0001,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:0.0001152,AFR_MAF=A:0,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,EA_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=A:0,cDNA_position=311,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs369434915,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:2.496e-05,HGVSc=ENST00000592654.1:c.-31G>A,ExAC_Adj_MAF=A:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	321	321	0.0	.	.	AC_Male=1;AF_NFE=2.58685e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|1|0|1|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.00000e-31;AF_OTH=0.00000e+00;alleles=G%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.06140e-05;Hom=0;AF_POPMAX=2.58685e-05;AN_POPMAX=77314;AC_NFE=2;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0|0|0|0;AF_Male=9.69330e-06;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.87363e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.17280e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=7.91480e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.21760e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=T,IMPACT=MODIFIER,EXON=2/4,cDNA_position=321,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-21G>T
CDS|ENST00000592654	VCF	5_prime_UTR_variant	322	322	0.0	.	.	AC_Male=0;AF_NFE=1.30774e-05;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.99526e-56;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.34920e-06;Hom=0;AF_POPMAX=1.30774e-05;AN_POPMAX=76468;AC_NFE=1;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=3.84615e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=65;AF_Female=1.18189e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=8.26907e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.10985e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=T,IMPACT=MODIFIER,EXON=2/4,cDNA_position=322,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-20C>T
CDS|ENST00000592654	VCF	5_prime_UTR_variant	323	323	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=5.01187e-83;AF_OTH=0.00000e+00;alleles=C%2CT;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.48408e-06;Hom=0;AF_POPMAX=9.03506e-05;AN_POPMAX=11068;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=9.03506e-05;AC_raw=1;AB_MEDIAN=6.75000e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=40;AF_Female=1.21150e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=6.96517e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=AFR;AC_POPMAX=1;AC_AFR=1;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11130e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=T:2.3e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,AMR_MAF=T:0.0008,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=T:0,AFR_MAF=T:0,FLAGS=cds_end_NF,EAS_MAF=T:0,EUR_MAF=T:0,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=T:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,GMAF=T:0.0002,STRAND=1,ExAC_SAS_MAF=T:0,Allele=T,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=T:0.0002112,cDNA_position=323,ExAC_NFE_MAF=T:0,SYMBOL=NMT1,Existing_variation=rs184508172,SAS_MAF=T:0,VARIANT_CLASS=SNV,AA_MAF=T:0,MINIMISED=1,ExAC_AFR_MAF=T:8.398e-06,HGVSc=ENST00000592654.1:c.-19C>T,ExAC_Adj_MAF=T:0
CDS|ENST00000592654	VCF	5_prime_UTR_variant	326	326	0.0	.	.	AC_Male=0;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=99;AB_HIST_ALT=0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=7.94328e-72;AF_OTH=0.00000e+00;alleles=G%2CC;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=1;Hom_NFE=0;AF=5.55759e-06;Hom=0;AF_POPMAX=3.91972e-05;AN_POPMAX=25512;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AF_Male=0.00000e+00;AF_AFR=0.00000e+00;AC_raw=1;AB_MEDIAN=4.82759e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=58;AF_Female=1.22730e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=3.91972e-05;AS_RF=8.51470e-01;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=1;POPMAX=SAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=4.11306e-06;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=C,IMPACT=MODIFIER,EXON=2/4,cDNA_position=326,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-16G>C
CDS|ENST00000592654	VCF	5_prime_UTR_variant	330	330	0.0	.	.	AC_Male=1;AF_NFE=0.00000e+00;Hom_FIN=0;GQ_MEDIAN=70;AB_HIST_ALT=0|0|0|0|1|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=3.97133e-05;AF_OTH=0.00000e+00;alleles=C%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.12740e-05;Hom=0;AF_POPMAX=8.46453e-05;AN_POPMAX=11814;AC_NFE=0;AS_FilterStatus=PASS;Hom_OTH=0;DP_HIST_ALT=0|0|0|1|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.03086e-05;AF_AFR=0.00000e+00;AC_raw=2;AB_MEDIAN=3.94118e-01;Hom_EAS=0;AC_AMR=1;AF_ASJ=0.00000e+00;DP_MEDIAN=24;AF_Female=1.24387e-05;GQ_HIST_ALT=0|0|0|0|0|0|0|0|1|0|0|0|0|0|0|0|0|0|0|1;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.04301e-01;Hom_AMR=0;AC_EAS=1;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=8.46453e-05;AC_SAS=0;POPMAX=EAS;AC_POPMAX=1;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=8.23113e-06;Hom_Female=0;AF_AMR=3.93236e-05;CSQ=ALLELE_NUM=1,SYMBOL_SOURCE=HGNC,ENSP=ENSP00000466827,UNIPARC=UPI0002841054,Consequence=5_prime_UTR_variant,TREMBL=K7EN82,Feature=ENST00000592654,STRAND=1,BIOTYPE=protein_coding,Allele=A,IMPACT=MODIFIER,EXON=2/4,cDNA_position=330,SYMBOL=NMT1,Gene=ENSG00000136448,HGNC_ID=7857,VARIANT_CLASS=SNV,FLAGS=cds_end_NF,Feature_type=Transcript,MINIMISED=1,HGVSc=ENST00000592654.1:c.-12C>A
CDS|ENST00000592654	VCF	5_prime_UTR_variant	336	336	0.0	.	.	AC_Male=1;AF_NFE=2.98686e-05;Hom_FIN=0;GQ_MEDIAN=66;AB_HIST_ALT=0|0|0|2|0|0|0|0|1|0|0|0|0|1|0|0|0|0|0|0;AC_FIN=0;DREF_MEDIAN=1.98974e-04;AF_OTH=0.00000e+00;alleles=G%2CA;AF_FIN=0.00000e+00;AC_OTH=0;Hom_Male=0;AC=2;Hom_NFE=0;AF=1.19832e-05;Hom=0;AF_POPMAX=2.98686e-05;AN_POPMAX=66960;AC_NFE=2;AS_FilterStatus=RF;Hom_OTH=0;DP_HIST_ALT=0|0|2|1|0|1|0|0|0|0|0|0|0|0|0|0|0|0|0|0;AF_Male=1.09965e-05;AF_AFR=0.00000e+00;AC_raw=4;AB_MEDIAN=3.15047e-01;Hom_EAS=0;AC_AMR=0;AF_ASJ=0.00000e+00;DP_MEDIAN=14;AF_Female=1.31645e-05;GQ_HIST_ALT=0|0|1|0|0|0|1|0|0|0|0|0|0|0|0|0|0|0|0|2;Hom_raw=0;AF_SAS=0.00000e+00;AS_RF=1.22455e-02;Hom_AMR=0;AC_EAS=0;AC_Female=1;Hom_AFR=0;Hom_ASJ=0;AF_EAS=0.00000e+00;AC_SAS=0;POPMAX=NFE;AC_POPMAX=2;AC_AFR=0;Hom_SAS=0;AC_ASJ=0;AF_raw=1.64978e-05;Hom_Female=0;AF_AMR=0.00000e+00;CSQ=ALLELE_NUM=1,UNIPARC=UPI0002841054,ExAC_EAS_MAF=A:2.776e-05,TREMBL=K7EN82,Feature=ENST00000592654,BIOTYPE=protein_coding,Gene=ENSG00000136448,HGNC_ID=7857,ExAC_OTH_MAF=A:5.974e-05,AFR_MAF=A:0,FLAGS=cds_end_NF,Feature_type=Transcript,SYMBOL_SOURCE=HGNC,ExAC_FIN_MAF=A:0,ENSP=ENSP00000466827,Consequence=5_prime_UTR_variant,STRAND=1,ExAC_SAS_MAF=A:0,Allele=A,IMPACT=MODIFIER,EXON=2/4,ExAC_AMR_MAF=A:0,cDNA_position=336,ExAC_NFE_MAF=A:0,SYMBOL=NMT1,Existing_variation=rs761306458,VARIANT_CLASS=SNV,MINIMISED=1,ExAC_AFR_MAF=A:8.569e-06,HGVSc=ENST00000592654.1:c.-6G>A,ExAC_Adj_MAF=A:0