| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.2570668T>A | CA007313 | KCNQ1 | c.257T>A (p.Val86Asp) c.478-12767T>A (n.478-12767T>A) c.518T>A (p.Val173Asp) c.137T>A (p.Val46Asp) c.124-12767T>A (n.124-12767T>A) | ClinVar dbSNP |
| 11 | g.2570668T= | CA1948239598 | KCNQ1 | c.257T= (p.Val86=) c.478-12767T= (n.478-12767T=) c.518T= (p.Val173=) c.137T= (p.Val46=) c.124-12767T= (n.124-12767T=) | dbSNP |