| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.123427951G>C | CA151420 | GRIA3 | c.1888G>C (p.Gly630Arg) n.5217+9299C>G | ClinVar dbSNP |
| X | g.123427951G>A | CA414259524 | GRIA3 | c.1888G>A (p.Gly630Arg) n.5217+9299C>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC |
| X | g.123427951G= | CA2455894159 | GRIA3 | c.1888G= (p.Gly630=) n.5217+9299C= | dbSNP |