Entering edit mode
5.4 years ago
c.clarido
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110
Hello community,
CSQ=T|intron_variant&non_coding_transcript_variant|MODIFIER|AL627309.1|ENSG00000238009|Transcript|ENST00000466430|lincRNA||2/3||||||||||-1||Clone_based_ensembl_gene||||||||||||||||||||||1:96806-96806|0.0024263|1:96806-96806&rs868804354|3.31236e-05&7.19867e-02,T|intron_variant&non_coding_transcript_variant|MODIFIER|AL627309.1|ENSG00000238009|Transcript|ENST00000477740|lincRNA||3/3||||||||||-1||Clone_based_ensembl_gene||||||||||||||||||||||1:96806-96806|0.0024263|1:96806-96806&rs868804354|3.31236e-05&7.19867e-02
Here I have a CSQ field of a variant. What does '&' mean here: 3.31236e-05&7.19867e-02,T ?
what is the definition header for
INFO=<ID=CSQ
? what are the column corresponding to your annotation ?I'm sorry, I don't understand what you mean. Do you perhaps mean this?:
yes (my messsage was messed-up by the biostar engine) , what is the column in the header corresponding to 3.31236e-05&7.19867e-02 ?
It is the gnomAD_AF I don't understand the format: AF1&AF2,T
is it this variant ? https://gnomad.broadinstitute.org/variant/1-96806-C-T
yes sir: rs868804354
I would have say that there are two alternative alleles at this position, or two values for genomes and exomes, but I don't even find the same AF values at that position in gnomad...