Variant #0000262947 (NC_000002.11:g.111921835A>G, NM_001204106.1:c.*27A>G (BCL2L11))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.111921835A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2L11_000044
Frequency 401/13006
Freq. EA 2/8600
Freq. AA 399/4406
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 16:22:05 +02:00 (CEST)
Date last edited 2013-05-03 23:13:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L11 NM_001204106.1 ?/? c.*27A>G r.(=) p.(=)