| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38606034G>A | CA16043398 | SCN5A | c.1255C>T (p.Gln419Ter) c.1126C>T (p.Gln376Ter) | ClinVar dbSNP |
| 3 | g.38606034G>C | CA352148654 | SCN5A | c.1255C>G (p.Gln419Glu) c.1126C>G (p.Gln376Glu) | ClinVar dbSNP |
| 3 | g.38606034G= | CA1358585952 | SCN5A | c.1255C= (p.Gln419=) c.1126C= (p.Gln376=) | dbSNP |