Variant #0000826911 (NC_000008.10:g.26265477T>C, NC_000008.10(NM_004331.2):c.358-39T>C (BNIP3L))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.26265477T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BNIP3L_000026
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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.358-39T>C r.(=) p.(=)