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I can't add VAF from population for all of my variants from VCF file

Good morning guys,

I am working on a genomics project, and I want to use the variant allelic frequency (VAF) from population to filter out germline variants from my VCF files. I tried with:

 bcftools annotate --annotations $gnomad_variants --columns AF --output $output --output-type v $input_gz

using the exome file (85Go) from gnomad website, because I work with WES data, but I only get 3000 VAF over 300k variants in my vcf.

Do you have any clue of how to get more VAF, and in a more efficient way, to annotate my VCF files better? I insist on the fact that I don't want to get my MAF but VAF from population.

Thank you very much,
Samuel

genomics vcf gnomad

you have 300k variants and you found only 3000 of them in gnomAD? Something went wrong. Can you share 10 of the ones that are missing?

Hi,

Thank you for your answer,

I got them using ANNOVAR, there you have some that have the AF= and the others don't

chr1    201123772   .   C   T   4.37899 .   DP=2;SGB=-0.379885;RPBZ=0;MQBZ=0;BQBZ=0;NMBZ=0;SCBZ=0;FS=0;MQ0F=0;AC=1;AN=2;DP4=1,0,1,0;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=intergenic;Gene.refGene=ASCL5\x3bTMEM9;GeneDetail.refGene=dist\x3d8400\x3bdist\x3d10999;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END   GT:PL:DP:AD:GP:GQ   0/1:35,0,35:2:1,1:0.000158064,0.999684,0.000158064:35
chr1    201135543   .   G   C   35.9326 .   DP=9;VDB=0.0221621;SGB=-0.511536;RPBZ=0.801784;MQBZ=0;BQBZ=0.46291;NMBZ=-0.707107;SCBZ=-0.707107;FS=0;MQ0F=0;AC=1;AN=2;DP4=6,0,3,0;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=UTR3;Gene.refGene=TMEM9;GeneDetail.refGene=NM_001288564:c.*120C>G\x3bNM_001288566:c.*120C>G\x3bNM_001288568:c.*120C>G\x3bNM_001288567:c.*120C>G\x3bNM_001288569:c.*120C>G\x3bNM_001288571:c.*120C>G\x3bNM_001288570:c.*120C>G\x3bNM_016456:c.*120C>G\x3bNM_001288565:c.*120C>G;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END GT:PL:DP:AD:GP:GQ   0/1:69,0,123:9:6,3:1.2249e-07,1,1.28777e-13:69
chr1    201145820   .   G   T   72.4148 .   DP=3;VDB=0.0221621;SGB=-0.511536;FS=0;MQ0F=0;AC=2;AN=2;DP4=0,0,3,0;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=intronic;Gene.refGene=TMEM9;GeneDetail.refGene=.;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END   GT:PL:DP:AD:GP:GQ   1/1:102,9,0:3:0,3:0,0,1:127
chr1    201157334   .   G   T   41.4148 .   DP=2;VDB=0.02;SGB=-0.453602;FS=0;MQ0F=0;AC=2;AN=2;DP4=0,0,0,2;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=intronic;Gene.refGene=TMEM9;GeneDetail.refGene=.;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END    GT:PL:DP:AD:GP:GQ   1/1:71,6,0:2:0,2:0,0,1:127
chr1    201174887   .   C   A   4.37899 .   DP=2;SGB=-0.379885;RPBZ=0;MQBZ=0;BQBZ=0;NMBZ=0;SCBZ=0;FS=0;MQ0F=0;AC=1;AN=2;DP4=1,0,1,0;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=intergenic;Gene.refGene=TMEM9\x3bIGFN1;GeneDetail.refGene=dist\x3d3305\x3bdist\x3d15937;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END   GT:PL:DP:AD:GP:GQ   0/1:35,0,35:2:1,1:0.000158064,0.999684,0.000158064:35
chr1    201177778   .   C   T   21.2837 .   DP=3;SGB=-0.379885;RPBZ=1;MQBZ=0;BQBZ=1;NMBZ=-1;SCBZ=0;FS=0;MQ0F=0;AC=1;AN=2;DP4=1,0,1,0;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=intergenic;Gene.refGene=TMEM9\x3bIGFN1;GeneDetail.refGene=dist\x3d6196\x3bdist\x3d13046;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END  GT:PL:DP:AD:GP:GQ   0/1:54,0,35:2:1,1:1.35988e-06,0.999767,0.000231332:36
chr1    201199934   .   T   C   155.487 .   DP=40;VDB=0.230965;SGB=-0.670168;RPBZ=-2.67353;MQBZ=0;MQSBZ=0;BQBZ=0.901457;NMBZ=0.363879;SCBZ=-0.856499;FS=0;MQ0F=0;AC=1;AN=2;DP4=8,20,5,5;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=intronic;Gene.refGene=IGFN1;GeneDetail.refGene=.;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END  GT:PL:DP:AD:GP:GQ   0/1:189,0,255:38:28,10:1.60505e-19,1,6.20086e-27:127
chr1    201209738   .   A   G   148.287 .   DP=246;VDB=0.212968;SGB=-0.693147;RPBZ=0.999561;MQBZ=-4.13408;MQSBZ=2.76703;BQBZ=0.718089;NMBZ=7.53256;SCBZ=2.22265;FS=0;MQ0F=0.0203252;AC=1;AN=2;DP4=140,31,59,10;MQ=51;ANNOVAR_DATE=2020-06-08;Func.refGene=exonic;Gene.refGene=IGFN1;GeneDetail.refGene=.;ExonicFunc.refGene=synonymous_SNV;AAChange.refGene=IGFN1:NM_001164586:exon12:c.A4845G:p.G1615G;ALLELE_END;AF=0.0758308 GT:PL:DP:AD:GP:GQ   0/1:182,0,255:240:171,64:8.91751e-19,1,5.59366e-27:127
chr1    201209776   .   A   G   144.974 .   DP=246;VDB=0.981223;SGB=-0.693147;RPBZ=-1.80167;MQBZ=-4.61034;MQSBZ=0.301843;BQBZ=0.822387;NMBZ=5.62233;SCBZ=-0.656655;FS=0;MQ0F=0.0772358;AC=1;AN=2;DP4=111,28,90,3;MQ=35;ANNOVAR_DATE=2020-06-08;Func.refGene=exonic;Gene.refGene=IGFN1;GeneDetail.refGene=.;ExonicFunc.refGene=nonsynonymous_SNV;AAChange.refGene=IGFN1:NM_001164586:exon12:c.A4883G:p.E1628G;ALLELE_END;AF=0.0860138    GT:PL:DP:AD:GP:GQ   0/1:178,0,255:232:139,89:1.50686e-18,1,8.31511e-27:127
chr1    201209796   .   A   G   176.111 .   DP=244;VDB=0.004529;SGB=-0.693147;RPBZ=-6.06726;MQBZ=-5.22149;MQSBZ=1.2987;BQBZ=0.536083;NMBZ=4.28046;SCBZ=-2.26132;FS=0;MQ0F=0.0860656;AC=1;AN=2;DP4=98,29,100,4;MQ=32;ANNOVAR_DATE=2020-06-08;Func.refGene=exonic;Gene.refGene=IGFN1;GeneDetail.refGene=.;ExonicFunc.refGene=nonsynonymous_SNV;AAChange.refGene=IGFN1:NM_001164586:exon12:c.A4903G:p.K1635E;ALLELE_END;AF=0.226855    GT:PL:DP:AD:GP:GQ   0/1:209,0,255:231:127,104:1.06277e-21,1,9.36485e-27:127
chr1    201225142   .   G   T   18.2553 .   DP=8;VDB=0.02;SGB=-0.453602;RPBZ=2.02424;MQBZ=0;MQSBZ=0;BQBZ=0.57735;NMBZ=0;SCBZ=0;FS=0;MQ0F=0;AC=1;AN=2;DP4=1,5,0,2;MQ=60;ANNOVAR_DATE=2020-06-08;Func.refGene=intronic;Gene.refGene=IGFN1;GeneDetail.refGene=.;ExonicFunc.refGene=.;AAChange.refGene=.;ALLELE_END GT:PL:DP:AD:GP:GQ   0/1:52,0,164:8:6,2:9.31038e-06,0.999991,6.74473e-18:50

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