| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38560170C>T | CA017985 | SCN5A | c.4219G>A (p.Gly1407Arg) c.4222G>A (p.Gly1408Arg) c.4060G>A (p.Gly1354Arg) c.4093G>A (p.Gly1365Arg) | ClinVar dbSNP gnomAD v4 |
| 3 | g.38560170C= | CA1358565651 | SCN5A | c.4219G= (p.Gly1407=) c.4222G= (p.Gly1408=) c.4060G= (p.Gly1354=) c.4093G= (p.Gly1365=) | dbSNP |
| 3 | g.38560170C>G | CA352146220 | SCN5A | c.4219G>C (p.Gly1407Arg) c.4222G>C (p.Gly1408Arg) c.4060G>C (p.Gly1354Arg) c.4093G>C (p.Gly1365Arg) | dbSNP |