| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.110914200C>G | CA009968 | MYL2 | c.260G>C (p.Gly87Ala) c.203G>C (p.Gly68Ala) c.218G>C (p.Gly73Ala) n.91G>C | ClinVar dbSNP |
| 12 | g.110914200C>T | CA386698668 | MYL2 | c.260G>A (p.Gly87Glu) c.203G>A (p.Gly68Glu) c.218G>A (p.Gly73Glu) n.91G>A | ClinVar dbSNP |
| 12 | g.110914200C= | CA2063072387 | MYL2 | c.260G= (p.Gly87=) c.203G= (p.Gly68=) c.218G= (p.Gly73=) n.91G= | dbSNP |