Variant #0000454904 (NC_000004.11:g.437761G>C, NM_133474.2:c.495C>G (ZNF721))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.437761G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF721_000125
Frequency 1/12850
Freq. EA 1/8552
Freq. AA 0/4298
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 2018-08-23 02:28:35 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF721 NM_133474.2 ?/? c.495C>G r.(?) p.(Tyr165*)
ABCA11P NR_002451.2 ?/? n.357-16999C>G r.(?) p.(Tyr165*)