Thanks for the answer and the link! The vcf file makes much more sense after reading that documentation you provided.
Pipes within VCF INFO Column
Sorry if this has been posted before but I cannot find an answer anywhere. I am trying to make sense of the INFO column of a .vcf file that was generated using whole exome sequencing (Illumina). Specifically, what do the number of pipes mean in the data below (| vs || vs ||||, etc.). Thanks!
ANN=A|intron_variant|MODIFIER|PSAP|5660|Transcript|NM_001042465.1|protein_coding||13/14|NM_001042465.1:c.1441-22C>T|||||||rs885828||-1||SNV|EntrezGene||YES||||NP_001035930.1|||||G|G||||||||10:g.73578503G>A|0.4062|0.4592|0.3689|0.5982|0.2793|0.2935|0.4392|0.2714|0.3389|0.4469|0.4446|0.2387|0.6208|0.3522|0.2768|0.3038|0.2545|0.6208|gnomAD_EAS|benign|||18639233||||,A|intron_variant|MODIFIER|PSAP|5660|Transcript|NM_001042465.2|protein_coding||13/14|NM_001042465.2:c.1441-22C>T|||||||rs885828||-1||SNV|EntrezGene||YES||||NP_001035930.1|||||G|G|OK|||||||10:g.73578503G>A|0.4062|0.4592|0.3689|0.5982|0.2793|0.2935|0.4392|0.2714|0.3389|0.4469|0.4446|0.2387|0.6208|0.3522|0.2768|0.3038|0.2545|0.6208|gnomAD_EAS|benign|||18639233||||,A|intron_variant|MODIFIER|PSAP|5660|Transcript|NM_001042466.1|protein_coding||13/14|NM_001042466.1:c.1438-22C>T|||||||rs885828||-1||SNV|EntrezGene||||||NP_001035931.1|||||G|G||||||||10:g.73578503G>A|0.4062|0.4592|0.3689|0.5982|0.2793|0.2935|0.4392|0.2714|0.3389|0.4469|0.4446|0.2387|0.6208|0.3522|0.2768|0.3038|0.2545|0.6208|gnomAD_EAS|benign|||18639233||||,A|intron_variant|MODIFIER|PSAP|5660|Transcript|NM_001042466.2|protein_coding||13/14|NM_001042466.2:c.1438-22C>T|||||||rs885828||-1||SNV|EntrezGene||||||NP_001035931.1|||||G|G|OK|||||||10:g.73578503G>A|0.4062|0.4592|0.3689|0.5982|0.2793|0.2935|0.4392|0.2714|0.3389|0.4469|0.4446|0.2387|0.6208|0.3522|0.2768|0.3038|0.2545|0.6208|gnomAD_EAS|benign|||18639233||||,A|intron_variant|MODIFIER|PSAP|5660|Transcript|NM_002778.2|protein_coding||12/13|NM_002778.2:c.1432-22C>T|||||||rs885828||-1||SNV|EntrezGene||||||NP_002769.1|||||G|G||||||||10:g.73578503G>A|0.4062|0.4592|0.3689|0.5982|0.2793|0.2935|0.4392|0.2714|0.3389|0.4469|0.4446|0.2387|0.6208|0.3522|0.2768|0.3038|0.2545|0.6208|gnomAD_EAS|benign|||18639233||||,A|intron_variant|MODIFIER|PSAP|5660|Transcript|NM_002778.3|protein_coding||12/13|NM_002778.3:c.1432-22C>T|||||||rs885828||-1||SNV|EntrezGene||||||NP_002769.1|||||G|G|OK|||||||10:g.73578503G>A|0.4062|0.4592|0.3689|0.5982|0.2793|0.2935|0.4392|0.2714|0.3389|0.4469|0.4446|0.2387|0.6208|0.3522|0.2768|0.3038|0.2545|0.6208|gnomAD_EAS|benign|||18639233||||
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pipe '|' is just a separator '||' means that there is a missing value.
You should have a look at the ANN spec for snpEff: http://snpeff.sourceforge.net/VCFannotationformat_v1.0.pdf
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it it answers you need, please validate+close by clicking the green mark on the left
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