| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38550967T>C | CA019212 | SCN5A | c.5402A>G (p.Asp1801Gly) c.5405A>G (p.Asp1802Gly) c.5351A>G (p.Asp1784Gly) c.5243A>G (p.Asp1748Gly) c.5306A>G (p.Asp1769Gly) c.5276A>G (p.Asp1759Gly) c.5348A>G (p.Asp1783Gly) | ClinVar dbSNP |
| 3 | g.38550967T>G | CA352141181 | SCN5A | c.5402A>C (p.Asp1801Ala) c.5405A>C (p.Asp1802Ala) c.5351A>C (p.Asp1784Ala) c.5243A>C (p.Asp1748Ala) c.5306A>C (p.Asp1769Ala) c.5276A>C (p.Asp1759Ala) c.5348A>C (p.Asp1783Ala) | dbSNP |