| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.101980418T>G | CA16043477 | DYNC1H1 | c.829T>G (p.Phe277Val) n.948T>G c.*338T>G (n.*338T>G) c.*560T>G (n.*560T>G) | ClinVar dbSNP |
| 14 | g.101980418T= | CA2159590747 | DYNC1H1 | c.829T= (p.Phe277=) n.948T= c.*338T= (n.*338T=) c.*560T= (n.*560T=) | dbSNP |