| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.13561125A>G | CA233131023 | GRIN2B | c.*1658T>C (n.*1658T>C) c.69+47478T>C (n.69+47478T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.13561125A= | CA2017436971 | GRIN2B | c.*1658T= (n.*1658T=) c.69+47478T= (n.69+47478T=) | dbSNP |