| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.123427954C>A | CA120935 | GRIA3 | c.1891C>A (p.Arg631Ser) n.5217+9296G>T | ClinVar dbSNP |
| X | g.123427954C>T | CA414259543 | GRIA3 | c.1891C>T (p.Arg631Cys) n.5217+9296G>A | ClinVar dbSNP gnomAD v4 |
| X | g.123427954C= | CA2455894160 | GRIA3 | c.1891C= (p.Arg631=) n.5217+9296G= | dbSNP |