| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9829485G>C | CA130441 | GRIN2A | c.1945C>G (p.Leu649Val) c.1474C>G (p.Leu492Val) n.1538C>G c.1534C>G (p.Leu512Val) n.1584C>G c.1786C>G (p.Leu596Val) c.1687C>G (p.Leu563Val) c.2101C>G (p.Leu701Val) | ClinVar dbSNP |
| 16 | g.9829485G= | CA2206726993 | GRIN2A | c.1945C= (p.Leu649=) c.1474C= (p.Leu492=) n.1538C= c.1534C= (p.Leu512=) n.1584C= c.1786C= (p.Leu596=) c.1687C= (p.Leu563=) c.2101C= (p.Leu701=) | dbSNP |