Variant #0001596134 (NC_000017.10:g.41258456A>G, NC_000017.10(NM_007294.3):c.212+17T>C (BRCA1))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.41258456A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BRCA1_000240
Frequency 1/12990
Freq. EA 0/8588
Freq. AA 1/4402
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 2013-05-05 17:52:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BRCA1 NM_007294.3 ?/? c.212+17T>C r.(=) p.(=)