| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.17387226C>G | CA277103 | KCNJ11 | c.605G>C (p.Gly202Ala) c.866G>C (p.Gly289Ala) n.1024G>C | ClinVar dbSNP |
| 11 | g.17387226C>A | CA277326 | KCNJ11 | c.605G>T (p.Gly202Val) c.866G>T (p.Gly289Val) n.1024G>T | ClinVar dbSNP COSMIC |
| 11 | g.17387226C= | CA1955119173 | KCNJ11 | c.605G= (p.Gly202=) c.866G= (p.Gly289=) n.1024G= | dbSNP |