Variant #0003025602 (NC_000004.11:g.438085G>T, NM_133474.3:c.171C>A (ZNF721))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.438085G>T
DB-ID -
dbSNP ID rs377359107
gnomAD frequency 2/245794
gnomAD homozygote count 0/122891
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF721 NM_133474.3 ./. c.171C>A r.(?) p.(Asn57Lys)
ABCA11P NR_002451.2 ./. n.357-17323C>A r.(=) p.(=)