| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73329725C>T | CA393093935 | HCN4 | c.1438G>A (p.Gly480Ser) c.220G>A (p.Gly74Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73329725C>G | CA117313 | HCN4 | c.1438G>C (p.Gly480Arg) c.220G>C (p.Gly74Arg) | ClinVar dbSNP |
| 15 | g.73329725C= | CA2187167635 | HCN4 | c.1438G= (p.Gly480=) c.220G= (p.Gly74=) | dbSNP |