Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.50342047G>A | CA214442 | ZMYND10 | c.967C>T (p.Gln323Ter) c.952C>T (p.Gln318Ter) c.838C>T (p.Gln280Ter) n.1122C>T n.53-116C>T c.730C>T (p.Gln244Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.50342047G= | CA1363902086 | ZMYND10 | c.967C= (p.Gln323=) c.952C= (p.Gln318=) c.838C= (p.Gln280=) n.1122C= n.53-116C= c.730C= (p.Gln244=) | dbSNP |