Variant #0001276031 (NC_000013.10:g.32972626A>T, NM_000059.3:c.9976A>T (BRCA2))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.32972626A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BRCA2_000419
Frequency 84/13006
Freq. EA 72/8600
Freq. AA 12/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:41:01 +02:00 (CEST)
Date last edited 2018-08-27 19:18:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ?/? c.9976A>T r.(?) p.(Lys3326*)