| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45461967C>T | CA359705027 | HCN1 | c.890G>A (p.Arg297Lys) n.53G>A | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45461967C>G | CA163274 | HCN1 | c.890G>C (p.Arg297Thr) n.53G>C | ClinVar dbSNP |
| 5 | g.45461967C= | CA1543688382 | HCN1 | c.890G= (p.Arg297=) n.53G= | dbSNP |