Variant #0000454479 (NC_000004.11:g.60070A>T, NC_000004.11(NM_182524.2):c.226+24A>T (ZNF595))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.60070A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF595_000009
Frequency 3/12952
Freq. EA 3/8596
Freq. AA 0/4356
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 2014-05-04 16:26:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF595 NM_182524.2 ?/? c.226+24A>T r.(=) p.(=)