Variant #0003022376 (NC_000004.11:g.59986C>G, NM_182524.2:c.166C>G (ZNF595))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.59986C>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/246256
gnomAD homozygote count 0/123127
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     
ZNF595 NM_182524.2 ./. c.166C>G r.(?) p.(Leu56Val)