Variant #0001596116 (NC_000017.10:g.41249297G>T, NM_007294.3:c.557C>A (BRCA1))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.41249297G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BRCA1_000222
Frequency 30/13002
Freq. EA 0/8596
Freq. AA 30/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2014-02-19 09:28:04 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BRCA1 NM_007294.3 ?/? c.557C>A r.(?) p.(Ser186Tyr)