| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9829589T>C | CA358154 | GRIN2A | c.1841A>G (p.Asn614Ser) c.1370A>G (p.Asn457Ser) n.1434A>G c.1430A>G (p.Asn477Ser) n.1480A>G c.1682A>G (p.Asn561Ser) c.1583A>G (p.Asn528Ser) c.1997A>G (p.Asn666Ser) | ClinVar dbSNP |
| 16 | g.9829589T= | CA2206727028 | GRIN2A | c.1841A= (p.Asn614=) c.1370A= (p.Asn457=) n.1434A= c.1430A= (p.Asn477=) n.1480A= c.1682A= (p.Asn561=) c.1583A= (p.Asn528=) c.1997A= (p.Asn666=) | dbSNP |