Variant #0001275623 (NC_000013.10:g.32893207T>A, NC_000013.10(NM_000059.3):c.68-7T>A (BRCA2))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.32893207T>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BRCA2_000011
Frequency 14/12932
Freq. EA 13/8574
Freq. AA 1/4358
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 2016-12-24 12:48:39 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ?/? c.68-7T>A r.(=) p.(=)