Variant #0001355177 (NC_000014.8:g.99737452C>T, NC_000014.8(NM_138576.2):c.58+46G>A (BCL11B))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.99737452C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL11B_000065
Frequency 2/12816
Freq. EA 0/8476
Freq. AA 2/4340
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 16:41:19 +02:00 (CEST)
Date last edited 2013-05-05 08:33:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL11B NM_138576.2 ?/? c.58+46G>A r.(=) p.(=)