| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.110911090T>C | CA010454 | MYL2 | c.488A>G (p.Glu163Gly) c.431A>G (p.Glu144Gly) c.446A>G (p.Glu149Gly) | ClinVar dbSNP |
| 12 | g.110911090T>G | CA010447 | MYL2 | c.488A>C (p.Glu163Ala) c.431A>C (p.Glu144Ala) c.446A>C (p.Glu149Ala) | ClinVar dbSNP |
| 12 | g.110911090T= | CA2063066592 | MYL2 | c.488A= (p.Glu163=) c.431A= (p.Glu144=) c.446A= (p.Glu149=) | dbSNP |