Variant #0000454538 (NC_000004.11:g.87033C>T, NM_182524.2:c.1638C>T (ZNF595))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.87033C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF595_000068
Frequency 1/12618
Freq. EA 1/8478
Freq. AA 0/4140
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 2014-03-27 15:42:02 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF595 NM_182524.2 ?/? c.1638C>T N/A N/A