| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.10180247C>T | CA16607095 | GRIN2A | c.165G>A (p.Trp55Ter) n.649G>A n.598G>A n.566G>A c.321G>A (p.Trp107Ter) | ClinVar dbSNP |
| 16 | g.10180247C>A | CA394715595 | GRIN2A | c.165G>T (p.Trp55Cys) n.649G>T n.598G>T n.566G>T c.321G>T (p.Trp107Cys) | dbSNP |