| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9840706G>A | CA145316 | GRIN2A | c.1592C>T (p.Thr531Met) c.1121C>T (p.Thr374Met) n.1185C>T n.2076C>T c.1181C>T (p.Thr394Met) n.1231C>T c.1433C>T (p.Thr478Met) c.1334C>T (p.Thr445Met) c.1748C>T (p.Thr583Met) | ClinVar dbSNP |
| 16 | g.9840706G>T | CA394800300 | GRIN2A | c.1592C>A (p.Thr531Lys) c.1121C>A (p.Thr374Lys) n.1185C>A n.2076C>A c.1181C>A (p.Thr394Lys) n.1231C>A c.1433C>A (p.Thr478Lys) c.1334C>A (p.Thr445Lys) c.1748C>A (p.Thr583Lys) | dbSNP |