Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38556460A>G | CA018241 | SCN5A | c.4415T>C (p.Phe1472Ser) c.4418T>C (p.Phe1473Ser) c.4364T>C (p.Phe1455Ser) c.4256T>C (p.Phe1419Ser) c.4289T>C (p.Phe1430Ser) c.4361T>C (p.Phe1454Ser) | ClinVar dbSNP |
3 | g.38556460A>C | CA018247 | SCN5A | c.4415T>G (p.Phe1472Cys) c.4418T>G (p.Phe1473Cys) c.4364T>G (p.Phe1455Cys) c.4256T>G (p.Phe1419Cys) c.4289T>G (p.Phe1430Cys) c.4361T>G (p.Phe1454Cys) | ClinVar dbSNP |