Variant #0000454864 (NC_000004.11:g.436991C>T, NM_133474.2:c.1265G>A (ZNF721))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.436991C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF721_000079
Frequency 1/12538
Freq. EA 1/8440
Freq. AA 0/4098
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 07:26:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF721 NM_133474.2 ?/? c.1265G>A r.(?) p.(Arg422His)
ABCA11P NR_002451.2 ?/? n.357-16229G>A r.(?) p.(Arg422His)