| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.13567146C>T | CA16619493 | GRIN2B | c.2477G>A (p.Gly826Glu) n.737G>A c.69+41457G>A (n.69+41457G>A) c.263G>A (p.Gly88Glu) | ClinVar dbSNP |
| 12 | g.13567146C= | CA2017439092 | GRIN2B | c.2477G= (p.Gly826=) n.737G= c.69+41457G= (n.69+41457G=) c.263G= (p.Gly88=) | dbSNP |