| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.17387595C>A | CA119833 | KCNJ11 | c.236G>T (p.Cys79Phe) c.497G>T (p.Cys166Phe) n.655G>T | ClinVar dbSNP |
| 11 | g.17387595C>T | CA341720 | KCNJ11 | c.236G>A (p.Cys79Tyr) c.497G>A (p.Cys166Tyr) n.655G>A | ClinVar dbSNP |
| 11 | g.17387595C= | CA1955119324 | KCNJ11 | c.236G= (p.Cys79=) c.497G= (p.Cys166=) n.655G= | dbSNP |