| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.46860702C>T | CA013722 | MYL3 | c.281G>A (p.Arg94His) n.503G>A n.239G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.46860702C= | CA1362297631 | MYL3 | c.281G= (p.Arg94=) n.503G= n.239G= | dbSNP |
| 3 | g.46860702C>G | CA352497878 | MYL3 | c.281G>C (p.Arg94Pro) n.503G>C n.239G>C | ClinVar dbSNP gnomAD v4 |