Variant #0000454847 (NC_000004.11:g.436601G>C, NM_133474.2:c.1655C>G (ZNF721))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.436601G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF721_000052
Frequency 1/12732
Freq. EA 0/8518
Freq. AA 1/4214
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 10:02:54 +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.1655C>G r.(?) p.(Thr552Ser)
ABCA11P NR_002451.2 ?/? n.357-15839C>G r.(?) p.(Thr552Ser)