| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45396550C>T | CA16044317 | HCN1 | c.1172G>A (p.Gly391Asp) n.335G>A | ClinVar dbSNP COSMIC |
| 5 | g.45396550C>A | CA359705262 | HCN1 | c.1172G>T (p.Gly391Val) n.335G>T | ClinVar dbSNP |
| 5 | g.45396550C= | CA1543652930 | HCN1 | c.1172G= (p.Gly391=) n.335G= | dbSNP |