| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.137156924G>A | CA153027 | GRIN1 | c.918G>A (p.Val306=) c.855G>A (p.Val285=) n.285G>A n.2365G>A c.901G>A (p.Gly301Arg) n.932G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.137156924G= | CA1630848147 | GRIN1 | c.918G= (p.Val306=) c.855G= (p.Val285=) n.285G= n.2365G= c.901G= (p.Gly301=) n.932G= | dbSNP |