Variant #0001275821 (NC_000013.10:g.32914044T>G, NM_000059.3:c.5552T>G (BRCA2))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.32914044T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BRCA2_000209
Frequency 2/13004
Freq. EA 2/8598
Freq. AA 0/4406
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 2018-08-23 00:27:41 +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.5552T>G r.(?) p.(Ile1851Ser)