| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9829487T>C | CA314939 | GRIN2A | c.1943A>G (p.Asn648Ser) c.1472A>G (p.Asn491Ser) n.1536A>G c.1532A>G (p.Asn511Ser) n.1582A>G c.1784A>G (p.Asn595Ser) c.1685A>G (p.Asn562Ser) c.2099A>G (p.Asn700Ser) | ClinVar dbSNP |
| 16 | g.9829487T= | CA2206726994 | GRIN2A | c.1943A= (p.Asn648=) c.1472A= (p.Asn491=) n.1536A= c.1532A= (p.Asn511=) n.1582A= c.1784A= (p.Asn595=) c.1685A= (p.Asn562=) c.2099A= (p.Asn700=) | dbSNP |