Variant #0000000103 (NC_000012.11:g.25380167C>T, NC_000012.11(NM_004985.3):c.290+1G>A (KRAS))

Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.25380167C>T
Reference -
DB-ID KRAS_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2020-06-23 13:17:50 +00:00 (UTC)
Date last edited 2020-07-09 12:09:02 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRAS NM_004985.3 ./? 3 c.290+1G>A r.spl? p.?
KRAS NM_033360.2 ./? 3 c.290+1G>A r.spl? p.?