| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.13865797C>A | CA384053400 | GRIN2B | c.411+1G>T (n.411+1G>T) | ClinVar dbSNP |
| 12 | g.13865797C>T | CA16609333 | GRIN2B | c.411+1G>A (n.411+1G>A) | ClinVar dbSNP |
| 12 | g.13865797C= | CA2017578155 | GRIN2B | c.411+1G= (n.411+1G=) | dbSNP |