Variant #0001076217 (NC_000011.9:g.32450032C>T, NC_000011.9(NM_000378.4):c.769+11G>A (WT1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.32450032C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID WT1_000052
Frequency 1/13002
Freq. EA 1/8598
Freq. AA 0/4404
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 10:28:20 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
WT1 NM_000378.4 ?/? c.769+11G>A r.(=) p.(=)