Variant #0000454539 (NC_000004.11:g.87055A>G, NM_182524.2:c.1660A>G (ZNF595))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.87055A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF595_000069
Frequency 1/12680
Freq. EA 0/8482
Freq. AA 1/4198
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 2014-03-02 15:59:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF595 NM_182524.2 ?/? c.1660A>G N/A N/A