Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.123465757G>T | CA414266320 | GRIA3 | c.2324+645G>T (n.2324+645G>T) c.2408G>T (p.Gly803Val) n.4959+997C>A | ClinVar dbSNP |
X | g.123465757G>A | CA16609121 | GRIA3 | c.2324+645G>A (n.2324+645G>A) c.2408G>A (p.Gly803Glu) n.4959+997C>T | ClinVar dbSNP |