Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.29673328G>ACA156041ZFP57c.783C>T (p.Cys261=)
c.567C>T (p.Cys189=)
c.531C>T (p.Cys177=)
c.723C>T (p.Cys241=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.29673328G>TCA251577ZFP57c.783C>A (p.Cys261Ter)
c.567C>A (p.Cys189Ter)
c.531C>A (p.Cys177Ter)
c.723C>A (p.Cys241Ter)
ClinVar dbSNP

Number of alleles fetched