| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.150951511C>T | CA005807 | KCNH2 | c.1882G>A (p.Gly628Ser) c.862G>A (p.Gly288Ser) c.1534G>A (p.Gly512Ser) c.1582G>A (p.Gly528Ser) c.1732G>A (p.Gly578Ser) c.1705G>A (p.Gly569Ser) | ClinVar dbSNP |
| 7 | g.150951511C>G | CA005813 | KCNH2 | c.1882G>C (p.Gly628Arg) c.862G>C (p.Gly288Arg) c.1534G>C (p.Gly512Arg) c.1582G>C (p.Gly528Arg) c.1732G>C (p.Gly578Arg) c.1705G>C (p.Gly569Arg) | ClinVar dbSNP |