Variant #0000454502 (NC_000004.11:g.86022del, NM_182524.2:c.627del (ZNF595))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.86022del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF595_000029
Frequency 4374/4520
Freq. EA 2940/3044
Freq. AA 1434/1476
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 16:25:12 +02:00 (CEST)
Date last edited 2014-04-28 05:56:31 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF595 NM_182524.2 ?/? c.627del r.(?) p.(Phe209Leufs*35)