Variant #0000454835 (NC_000004.11:g.436348A>G, NM_133474.2:c.1908T>C (ZNF721))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.436348A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF721_000065
Frequency 2/12396
Freq. EA 0/8378
Freq. AA 2/4018
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 05:15:55 +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.1908T>C r.(=) p.(=)
ABCA11P NR_002451.2 ?/? n.357-15586T>C r.(=) p.(=)