Variant #0000809710 (NC_000008.10:g.194679G>C, NM_173539.2:c.284G>C (ZNF596))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.194679G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF596_000045
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 16:29:29 +02:00 (CEST)
Date last edited 2014-05-22 00:25:25 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF596 NM_173539.2 ?/? c.284G>C r.(?) p.(Gly95Ala)