Variant #0001179695 (NC_000012.11:g.12247880T>G, NC_000012.11(NM_030766.1):c.*339+16T>G (BCL2L14))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.12247880T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2L14_000063
Frequency 1/12986
Freq. EA 1/8586
Freq. AA 0/4400
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 01:48:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L14 NM_030766.1 ?/? c.*339+16T>G r.(=) p.(=)