Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.29673368C>T | CA251583 | ZFP57 | c.743G>A (p.Arg248His) c.527G>A (p.Arg176His) c.491G>A (p.Arg164His) c.683G>A (p.Arg228His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.29673368C= | CA1618399091 | ZFP57 | c.743G= (p.Arg248=) c.527G= (p.Arg176=) c.491G= (p.Arg164=) c.683G= (p.Arg228=) | dbSNP |