Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.122284272T>G | CA119495 | CASR | c.2087T>G (p.Leu696Arg) c.2348T>G (p.Leu783Arg) c.2318T>G (p.Leu773Arg) c.1835T>G (p.Leu612Arg) c.1730T>G (p.Leu577Arg) | ClinVar dbSNP |
3 | g.122284272T= | CA1397872068 | CASR | c.2087T= (p.Leu696=) c.2348T= (p.Leu783=) c.2318T= (p.Leu773=) c.1835T= (p.Leu612=) c.1730T= (p.Leu577=) | dbSNP |