| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.150974797G>C | CA006358 | KCNH2 | c.221C>G (p.Thr74Arg) c.44C>G (p.Thr15Arg) n.444C>G | ClinVar dbSNP |
| 7 | g.150974797G>A | CA006365 | KCNH2 | c.221C>T (p.Thr74Met) c.44C>T (p.Thr15Met) n.444C>T | ClinVar dbSNP |
| 7 | g.150974797G= | CA1752462227 | KCNH2 | c.221C= (p.Thr74=) c.44C= (p.Thr15=) n.444C= | dbSNP |