| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.63941915C>T | CA117849 | SCN4A | c.4367G>A (p.Gly1456Glu) | ClinVar dbSNP |
| 17 | g.63941915C= | CA2270161171 | SCN4A | c.4367G= (p.Gly1456=) | dbSNP |
| 17 | g.63941915C>A | CA400616151 | SCN4A | c.4367G>T (p.Gly1456Val) | ClinVar dbSNP |