Variant #0000826930 (NC_000008.10:g.26267861T>C, NC_000008.10(NM_004331.2):c.612-19T>C (BNIP3L))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.26267861T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BNIP3L_000045
Frequency 1/13006
Freq. EA 0/8600
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 14:30:16 +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.612-19T>C r.(=) p.(=)