| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9829585G>T | CA128602 | GRIN2A | c.1845C>A (p.Asn615Lys) c.1374C>A (p.Asn458Lys) n.1438C>A c.1434C>A (p.Asn478Lys) n.1484C>A c.1686C>A (p.Asn562Lys) c.1587C>A (p.Asn529Lys) c.2001C>A (p.Asn667Lys) | ClinVar dbSNP |
| 16 | g.9829585G= | CA2206727026 | GRIN2A | c.1845C= (p.Asn615=) c.1374C= (p.Asn458=) n.1438C= c.1434C= (p.Asn478=) n.1484C= c.1686C= (p.Asn562=) c.1587C= (p.Asn529=) c.2001C= (p.Asn667=) | dbSNP |