Variant #0000454551 (NC_000004.11:g.87368A>G, NM_182524.2:c.*28A>G (ZNF595))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.87368A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF595_000081
Frequency 1/12328
Freq. EA 0/8346
Freq. AA 1/3982
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 2014-05-23 14:25:23 +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.*28A>G r.(=) p.(=)