Variant #0001514387 (NC_000016.9:g.75269765G>A, NM_014567.3:c.1032C>T (BCAR1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.75269765G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCAR1_000126
Frequency 1/12782
Freq. EA 1/8472
Freq. AA 0/4310
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 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 14:39:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCAR1 NM_014567.3 ?/? c.1032C>T r.(=) p.(=)