Variant #0001039530 (NC_000010.10:g.133786587C>T, NM_004052.2:c.233G>A (BNIP3))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.133786587C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BNIP3_000031
Frequency 37/13006
Freq. EA 0/8600
Freq. AA 37/4406
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 21:00:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BNIP3 NM_004052.2 ?/? c.233G>A r.(?) p.(Arg78Lys)