Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.29673328G>A | CA156041 | ZFP57 | c.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 |
6 | g.29673328G>T | CA251577 | ZFP57 | c.783C>A (p.Cys261Ter) c.567C>A (p.Cys189Ter) c.531C>A (p.Cys177Ter) c.723C>A (p.Cys241Ter) | ClinVar dbSNP |