Variant #0000454852 (NC_000004.11:g.436697C>G, NM_133474.2:c.1559G>C (ZNF721))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.436697C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF721_000062
Frequency 1/12664
Freq. EA 0/8490
Freq. AA 1/4174
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 00:05:11 +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.1559G>C r.(?) p.(Arg520Thr)
ABCA11P NR_002451.2 ?/? n.357-15935G>C r.(?) p.(Arg520Thr)