Variant #0001039532 (NC_000010.10:g.133786611G>A, NM_004052.2:c.209C>T (BNIP3))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.133786611G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BNIP3_000033
Frequency 2/13006
Freq. EA 1/8600
Freq. AA 1/4406
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BNIP3 NM_004052.2 ?/? c.209C>T r.(?) p.(Ser70Leu)