| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9822382T>C | CA314943 | GRIN2A | c.2050A>G (p.Thr684Ala) c.1579A>G (p.Thr527Ala) n.1643A>G c.1639A>G (p.Thr547Ala) n.1689A>G c.1891A>G (p.Thr631Ala) c.1792A>G (p.Thr598Ala) c.2206A>G (p.Thr736Ala) | ClinVar dbSNP |
| 16 | g.9822382T= | CA2206723647 | GRIN2A | c.2050A= (p.Thr684=) c.1579A= (p.Thr527=) n.1643A= c.1639A= (p.Thr547=) n.1689A= c.1891A= (p.Thr631=) c.1792A= (p.Thr598=) c.2206A= (p.Thr736=) | dbSNP |