| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.110913324C>A | CA010026 | MYL2 | c.275G>T (p.Gly92Val) c.218G>T (p.Gly73Val) c.233G>T (p.Gly78Val) n.106G>T | ClinVar dbSNP |
| 12 | g.110913324C>T | CA386698175 | MYL2 | c.275G>A (p.Gly92Glu) c.218G>A (p.Gly73Glu) c.233G>A (p.Gly78Glu) n.106G>A | ClinVar dbSNP |
| 12 | g.110913324C= | CA2063070958 | MYL2 | c.275G= (p.Gly92=) c.218G= (p.Gly73=) c.233G= (p.Gly78=) n.106G= | dbSNP |