Variant #0001142888 (NC_000011.9:g.111228602C>A, NC_000011.9(NM_006235.2):c.148-40G>T (POU2AF1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.111228602C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID POU2AF1_000038
Frequency 1029/12988
Freq. EA 538/8592
Freq. AA 491/4396
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.148-40G>T r.(=) p.(=)