| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.110915781T>C | CA009829 | MYL2 | c.103A>G (p.Ile35Val) c.46A>G (p.Ile16Val) c.94-1457A>G (n.94-1457A>G) | ClinVar dbSNP gnomAD v4 |
| 12 | g.110915781T>G | CA386699555 | MYL2 | c.103A>C (p.Ile35Leu) c.46A>C (p.Ile16Leu) c.94-1457A>C (n.94-1457A>C) | dbSNP gnomAD v4 |
| 12 | g.110915781T= | CA2063075033 | MYL2 | c.103A= (p.Ile35=) c.46A= (p.Ile16=) c.94-1457A= (n.94-1457A=) | dbSNP |