| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.150949031C>G | CA006729 | KCNH2 | n.3250G>C c.2417G>C (p.Gly806Ala) c.1397G>C (p.Gly466Ala) c.2117G>C (p.Gly706Ala) c.2267G>C (p.Gly756Ala) c.2240G>C (p.Gly747Ala) | ClinVar dbSNP |
| 7 | g.150949031C>T | CA006718 | KCNH2 | n.3250G>A c.2417G>A (p.Gly806Glu) c.1397G>A (p.Gly466Glu) c.2117G>A (p.Gly706Glu) c.2267G>A (p.Gly756Glu) c.2240G>A (p.Gly747Glu) | ClinVar dbSNP |