| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38609776C>T | CA019920 | SCN5A | c.892G>A (p.Gly298Ser) c.763G>A (p.Gly255Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38609776C>G | CA352150398 | SCN5A | c.892G>C (p.Gly298Arg) c.763G>C (p.Gly255Arg) | dbSNP |
| 3 | g.38609776C= | CA1358587645 | SCN5A | c.892G= (p.Gly298=) c.763G= (p.Gly255=) | dbSNP |