Variant #0001076212 (NC_000011.9:g.32449540G>A, NM_000378.4:c.834C>T (WT1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.32449540G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID WT1_000053
Frequency 4/12980
Freq. EA 0/8586
Freq. AA 4/4394
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 2019-04-09 10:28:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
WT1 NM_000378.4 ?/? c.834C>T r.? p.?