| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73329719C>T | CA202778 | HCN4 | c.1444G>A (p.Gly482Arg) c.226G>A (p.Gly76Arg) | ClinVar dbSNP |
| 15 | g.73329719C>G | CA16043942 | HCN4 | c.1444G>C (p.Gly482Arg) c.226G>C (p.Gly76Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329719C= | CA2187167606 | HCN4 | c.1444G= (p.Gly482=) c.226G= (p.Gly76=) | dbSNP |