Variant #0000826903 (NC_000008.10:g.26248986G>A, NC_000008.10(NM_004331.2):c.284+44G>A (BNIP3L))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.26248986G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BNIP3L_000018
Frequency 225/13006
Freq. EA 204/8600
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 14:30:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BNIP3L NM_004331.2 ?/? c.284+44G>A r.(=) p.(=)