| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.122282161G>A | CA119547 | CASR | c.1426G>A (p.Gly476Arg) c.1687G>A (p.Gly563Arg) c.1657G>A (p.Gly553Arg) c.1174G>A (p.Gly392Arg) c.1069G>A (p.Gly357Arg) | ClinVar dbSNP |
| 3 | g.122282161G= | CA1397885808 | CASR | c.1426G= (p.Gly476=) c.1687G= (p.Gly563=) c.1657G= (p.Gly553=) c.1174G= (p.Gly392=) c.1069G= (p.Gly357=) | dbSNP |