| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38585690C>A | CA16611280 | SCN5A | c.2787+1G>T (n.2787+1G>T) c.2658+1G>T (n.2658+1G>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38585690C= | CA1358577375 | SCN5A | c.2787+1G= (n.2787+1G=) c.2658+1G= (n.2658+1G=) | dbSNP |