Variant #0001039501 (NC_000010.10:g.133782067A>G, NM_004052.2:c.546T>C (BNIP3))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.133782067A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BNIP3_000002
Frequency 21/13006
Freq. EA 0/8600
Freq. AA 21/4406
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 16:30:47 +02:00 (CEST)
Date last edited 2013-05-04 21:00:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BNIP3 NM_004052.2 ?/? c.546T>C r.(=) p.(=)