Variant #0000454484 (NC_000004.11:g.85689T>C, NM_182524.2:c.294T>C (ZNF595))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.85689T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF595_000014
Frequency 1/12602
Freq. EA 1/8490
Freq. AA 0/4112
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 2014-06-12 11:45:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF595 NM_182524.2 ?/? c.294T>C r.(=) p.(=)