| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9829476A>C | CA145319 | GRIN2A | c.1954T>G (p.Phe652Val) c.1483T>G (p.Phe495Val) n.1547T>G c.1543T>G (p.Phe515Val) n.1593T>G c.1795T>G (p.Phe599Val) c.1696T>G (p.Phe566Val) c.2110T>G (p.Phe704Val) | ClinVar dbSNP |
| 16 | g.9829476A= | CA2206726990 | GRIN2A | c.1954T= (p.Phe652=) c.1483T= (p.Phe495=) n.1547T= c.1543T= (p.Phe515=) n.1593T= c.1795T= (p.Phe599=) c.1696T= (p.Phe566=) c.2110T= (p.Phe704=) | dbSNP |