| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.63442411C>G | CA16621790 | KCNQ2 | c.811G>C (p.Gly271Arg) n.549G>C c.292G>C (p.Gly98Arg) c.469G>C (p.Gly157Arg) n.937G>C c.176G>C c.232G>C (p.Gly78Arg) n.636G>C c.690+2248G>C (n.690+2248G>C) c.742G>C (p.Gly248Arg) | ClinVar dbSNP |
| 20 | g.63442411C>T | CA409653339 | KCNQ2 | c.811G>A (p.Gly271Ser) n.549G>A c.292G>A (p.Gly98Ser) c.469G>A (p.Gly157Ser) n.937G>A c.176G>A c.232G>A (p.Gly78Ser) n.636G>A c.690+2248G>A (n.690+2248G>A) c.742G>A (p.Gly248Ser) | ClinVar dbSNP |
| 20 | g.63442411C= | CA2374793473 | KCNQ2 | c.811G= (p.Gly271=) n.549G= c.292G= (p.Gly98=) c.469G= (p.Gly157=) n.937G= c.176G= c.232G= (p.Gly78=) n.636G= c.690+2248G= (n.690+2248G=) c.742G= (p.Gly248=) | dbSNP |