Hello Friends
I have created vcf file for my samples using GATK. After variant calling i used snpEff for annotation.
Now my vcf annotation files has :-
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT
in my format column there is information regarding to effect predicted by snpeff
I want a way to seperate this effects with my chrom pos id ref alt qual
means my file should have number of RSid having similar effect like synonymous variants etc
any help Thanks
1 answer
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Cancer_L001 chr1 976554 rs19127 C G 197.77 PASS ABHet=0.500;AC=1;AF=0.500;AN=2;BaseQRankSum=-1.068;DB;DP=24;Dels=0.00;ExcessHet=3.0103;FS=0.000;HaplotypeScore=0.0000;MLEAC=1;MLEAF=0.500;MQ=60.00;MQ0=0;MQRankSum=-0.491;QD=8.24;ReadPosRankSum=-1.415;SOR=0.446;ANN=G|splice_region_variant&synonymous_variant|LOW|AGRN|AGRN|transcript|NM_001305275.1|protein_coding|5/38|c.729C>G|p.Gly243Gly|779/7392|729/6204|243/2067||WARNING_TRANSCRIPT_MULTIPLE_STOP_CODONS,G|splice_region_variant&synonymous_variant|LOW|AGRN|AGRN|transcript|NM_198576.3|protein_coding|5/36|c.729C>G|p.Gly243Gly|779/7326|729/6138|243/2045|| GT:AD:DP:GQ:PL 0/1:12,12:24:99:226,0,265
and i tried java -jar ~/tools/snpEff/SnpSift.jar extractFields Mysample.ann.vcf CHROM POS ID REF AF FILTER ANN[].EFFECT ANN[].IMPACT > test.ann.vcf
after this when i open my test.ann.vcf file it looks like this
CHROM POS ID REF AF FILTER ANN[].EFFECT ANN[].IMPACT
chr1 976554 rs19127 C 0.5 PASS splice_region_variant&synonymous_variant splice_region_variant&synonymous_variant LOW LOW
means it has shifted one column ahead splice_region_variant&synonymous_variant splice_region_variant&synonymous_variant should be in ANN[].EFFECT column and LOW LOW in ANN[].IMPACT. But it has shifted one column ahead
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Would you mind posting few lines of your
vcf file, and also what you've tried so far?