| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9764617T>C | CA10588015 | GRIN2A | c.2927A>G (p.Asn976Ser) c.2456A>G (p.Asn819Ser) n.2520A>G c.*297A>G (n.*297A>G) c.2516A>G (p.Asn839Ser) n.2566A>G c.2768A>G (p.Asn923Ser) c.2669A>G (p.Asn890Ser) c.3083A>G (p.Asn1028Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.9764617T= | CA2206693328 | GRIN2A | c.2927A= (p.Asn976=) c.2456A= (p.Asn819=) n.2520A= c.*297A= (n.*297A=) c.2516A= (p.Asn839=) n.2566A= c.2768A= (p.Asn923=) c.2669A= (p.Asn890=) c.3083A= (p.Asn1028=) | dbSNP |