Variant #0001076210 (NC_000011.9:g.32449486C>T, NC_000011.9(NM_000378.4):c.872+16G>A (WT1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.32449486C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID WT1_000049
Frequency 3729/12988
Freq. EA 1242/8592
Freq. AA 2487/4396
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 2013-05-04 22:12:11 +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.872+16G>A r.(=) p.(=)