Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.243552928C>A | CA345670430 | AKT3 | c.964G>T (p.Asp322Tyr) c.895G>T (p.Asp299Tyr) c.721G>T (p.Asp241Tyr) c.781G>T (p.Asp261Tyr) n.1975G>T c.838G>T (p.Asp280Tyr) c.1067G>T (n.1067G>T) c.274G>T (p.Asp92Tyr) | ClinVar dbSNP |
1 | g.243552928C>T | CA16617120 | AKT3 | c.964G>A (p.Asp322Asn) c.895G>A (p.Asp299Asn) c.721G>A (p.Asp241Asn) c.781G>A (p.Asp261Asn) n.1975G>A c.838G>A (p.Asp280Asn) c.1067G>A (n.1067G>A) c.274G>A (p.Asp92Asn) | ClinVar dbSNP |