Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.64809792A>G | CA475163496 | MEN1 | c.318T>C (p.Tyr106=) c.79T>C n.350T>C n.70T>C n.358T>C n.385T>C c.44T>C | dbSNP |
11 | g.64809792A>T | CA16613689 | MEN1 | c.318T>A (p.Tyr106Ter) c.79T>A n.350T>A n.70T>A n.358T>A n.385T>A c.44T>A | ClinVar dbSNP |