| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38606058C>T | CA014560 | SCN5A | c.1231G>A (p.Val411Met) c.1102G>A (p.Val368Met) | ClinVar dbSNP |
| 3 | g.38606058C= | CA1358585963 | SCN5A | c.1231G= (p.Val411=) c.1102G= (p.Val368=) | dbSNP |
| 3 | g.38606058C>G | CA352148742 | SCN5A | c.1231G>C (p.Val411Leu) c.1102G>C (p.Val368Leu) | dbSNP |