| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.150974825T>G | CA006061 | KCNH2 | c.193A>C (p.Thr65Pro) c.16A>C (p.Thr6Pro) n.416A>C | ClinVar dbSNP |
| 7 | g.150974825T>C | CA369865663 | KCNH2 | c.193A>G (p.Thr65Ala) c.16A>G (p.Thr6Ala) n.416A>G | dbSNP |
| 7 | g.150974825T= | CA1752440883 | KCNH2 | c.193A= (p.Thr65=) c.16A= (p.Thr6=) n.416A= | dbSNP |
| 7 | g.150974825T>A | CA369865660 | KCNH2 | c.193A>T (p.Thr65Ser) c.16A>T (p.Thr6Ser) n.416A>T | dbSNP |