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Description
Using:
VariantAnnotation_1.49.1txdb = AnnotationHub::AnnotationHub()[["AH100643"]](UCSC seq styles)genome = BSgenome.Hsapiens.NCBI.GRCh38::BSgenome.Hsapiens.NCBI.GRCh38(UCSC seq styles)
I've got the following variant:
chr1:3826659-3826710 (genomic)
"CGATTCTTTACACACCCCAGTTCTTTGTGCACCCCAATTCTTTACATACCCT" (ref) -> "C" (alt)
( ^ exon 16 end <--- )
This overlaps transcript ENST00000378230, which has the following exons:
seqnames ranges strand | exon_id exon_rank
<Rle> <IRanges> <Rle> | <character> <integer>
chr1 3829266-3829373 - | ENSE00001690217 15
chr1 3826708-3826744 - | ENSE00001730754 16
chr1 3826370-3826436 - | ENSE00001769704 17
so the deletion only partially affects exon 16, and then the intron after. The predictCoding function reports:
REFCODON: CAGGACATTCAAGGAGGGAAAGCAGCCCCTGCTGAAGCTCTGGGAATCCCGGAT (= QDIQGGKAAPAEALGIPD)
VARCODON: CGT (= R; GT from extending into the intron?)
CDSLOC: 2186-2188
The sequence of each exon listed above is:
15: GCACGGAGAAAAGCGGCTACAGAAGAAGCAGAAAAACAAAAGAAAGAAGAAATAAAAGCTTTACAAGGGCAGCTGGCAGCACTGAAAGAAATTCAGGCTGAAGTTCAG
16: GAAAAAGAAAGTGATGCTGTGAAGCCAAAGAATCAGG [AGG = revcomp of variant end]
^ refcodon start
17: ACATTCAAGGAGGGAAAGCAGCCCCTGCTGAAGCTCTGGGAATCCCGGATGAGCACTATCTAGATAA
refcodon end ^ (but this exon should not be altered)
So this looks like VariantAnnotation incorrectly extends the REFCODON from one exon to the next, while the VARCODON extens into the (deleted part of the) intron?
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