| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38551289G>A | CA352142443 | SCN5A | c.5080C>T (p.Gln1694Ter) c.5083C>T (p.Gln1695Ter) c.5029C>T (p.Gln1677Ter) c.4921C>T (p.Gln1641Ter) c.4984C>T (p.Gln1662Ter) c.4954C>T (p.Gln1652Ter) c.5026C>T (p.Gln1676Ter) | ClinVar dbSNP |
| 3 | g.38551289G= | CA1358557779 | SCN5A | c.5080C= (p.Gln1694=) c.5083C= (p.Gln1695=) c.5029C= (p.Gln1677=) c.4921C= (p.Gln1641=) c.4984C= (p.Gln1662=) c.4954C= (p.Gln1652=) c.5026C= (p.Gln1676=) | dbSNP |