Variant #0003025596 (NC_000004.11:g.438080C>A, NM_133474.3:c.176G>T (ZNF721))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.438080C>A
DB-ID -
dbSNP ID rs75465770
gnomAD frequency 441/245860
gnomAD homozygote count 6/122495
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF721 NM_133474.3 ./. c.176G>T r.(?) p.(Cys59Phe)
ABCA11P NR_002451.2 ./. n.357-17318G>T r.(=) p.(=)