| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38603887G>T | CA015266 | SCN5A | c.1715C>A (p.Ala572Asp) c.1586C>A (p.Ala529Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38603887G>C | CA72939170 | SCN5A | c.1715C>G (p.Ala572Gly) c.1586C>G (p.Ala529Gly) | ClinVar dbSNP gnomAD v4 |
| 3 | g.38603887G>A | CA015275 | SCN5A | c.1715C>T (p.Ala572Val) c.1586C>T (p.Ala529Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38603887G= | CA1358584945 | SCN5A | c.1715C= (p.Ala572=) c.1586C= (p.Ala529=) | dbSNP |