Variant #0003022397 (NC_000004.11:g.85675T>G, NM_182524.2:c.280T>G (ZNF595))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.85675T>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/245280
gnomAD homozygote count 0/122639
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     
ZNF595 NM_182524.2 ./. c.280T>G r.(?) p.(Ser94Ala)