| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.150947011G>A | CA458644744 | KCNH2 | n.4029C>T c.3196C>T (p.Leu1066=) c.2176C>T (p.Leu726=) c.2896C>T (p.Leu966=) c.3046C>T (p.Leu1016=) c.3019C>T (p.Leu1007=) | ClinVar dbSNP |
| 7 | g.150947011G>C | CA008093 | KCNH2 | n.4029C>G c.3196C>G (p.Leu1066Val) c.2176C>G (p.Leu726Val) c.2896C>G (p.Leu966Val) c.3046C>G (p.Leu1016Val) c.3019C>G (p.Leu1007Val) | ClinVar dbSNP |