| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.10180098T>C | CA204473 | GRIN2A | c.314A>G (p.Asp105Gly) n.798A>G n.747A>G n.715A>G c.470A>G (p.Asp157Gly) | ClinVar dbSNP |
| 16 | g.10180098T>G | CA394715286 | GRIN2A | c.314A>C (p.Asp105Ala) n.798A>C n.747A>C n.715A>C c.470A>C (p.Asp157Ala) | dbSNP |
| 16 | g.10180098T>A | CA394715287 | GRIN2A | c.314A>T (p.Asp105Val) n.798A>T n.747A>T n.715A>T c.470A>T (p.Asp157Val) | dbSNP |
| 16 | g.10180098T= | CA2206912416 | GRIN2A | c.314A= (p.Asp105=) n.798A= n.747A= n.715A= c.470A= (p.Asp157=) | dbSNP |