Variant #0001142892 (NC_000011.9:g.111229483A>T, NC_000011.9(NM_006235.2):c.147+30T>A (POU2AF1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.111229483A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID POU2AF1_000046
Frequency 595/12902
Freq. EA 484/8546
Freq. AA 111/4356
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 16:37:25 +02:00 (CEST)
Date last edited 2013-05-05 00:26:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
POU2AF1 NM_006235.2 ?/? c.147+30T>A r.(=) p.(=)