| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.36058795G>A | CA259979 | WDR62 | c.193G>A (p.Val65Met) n.257G>A n.202G>A n.516G>A n.284G>A c.175G>A (p.Val59Met) | ClinVar dbSNP |
| 19 | g.36058795G= | CA2333949807 | WDR62 | c.193G= (p.Val65=) n.257G= n.202G= n.516G= n.284G= c.175G= (p.Val59=) | dbSNP |