| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.128911776T>A | CA383248667 | KCNJ5 | c.503T>A (p.Leu168His) | dbSNP |
| 11 | g.128911776T>G | CA232154 | KCNJ5 | c.503T>G (p.Leu168Arg) | ClinVar dbSNP COSMIC |
| 11 | g.128911776T= | CA2008292708 | KCNJ5 | c.503T= (p.Leu168=) | dbSNP |