| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.13567228C>T | CA16043466 | GRIN2B | c.2395G>A (p.Gly799Ser) n.655G>A c.69+41375G>A (n.69+41375G>A) c.181G>A (p.Gly61Ser) | ClinVar dbSNP |
| 12 | g.13567228C= | CA2017439127 | GRIN2B | c.2395G= (p.Gly799=) n.655G= c.69+41375G= (n.69+41375G=) c.181G= (p.Gly61=) | dbSNP |