| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38551391C>T | CA018812 | SCN5A | c.4978G>A (p.Gly1660Arg) c.4981G>A (p.Gly1661Arg) c.4927G>A (p.Gly1643Arg) c.4819G>A (p.Gly1607Arg) c.4882G>A (p.Gly1628Arg) c.4852G>A (p.Gly1618Arg) c.4924G>A (p.Gly1642Arg) | ClinVar dbSNP gnomAD v4 |
| 3 | g.38551391C>G | CA018819 | SCN5A | c.4978G>C (p.Gly1660Arg) c.4981G>C (p.Gly1661Arg) c.4927G>C (p.Gly1643Arg) c.4819G>C (p.Gly1607Arg) c.4882G>C (p.Gly1628Arg) c.4852G>C (p.Gly1618Arg) c.4924G>C (p.Gly1642Arg) | ClinVar dbSNP gnomAD v4 |