Variant #0000000042 (NC_000013.10:g.32969071G>C, NC_000013.10(NM_000059.3):c.9501+1G>C (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.32969071G>C
Reference -
DB-ID BRCA2_000013
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 2018-12-07 11:21:44 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ./+? 25 c.9501+1G>C r.spl? p.?