| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.25891855T>C | CA127801 | APP | n.2045A>G n.475A>G n.744A>G c.2078A>G (p.Glu693Gly) c.1853A>G (p.Glu618Gly) c.1685A>G (p.Glu562Gly) c.2021A>G (p.Glu674Gly) c.2024A>G (p.Glu675Gly) c.1748A>G (p.Glu583Gly) c.1910A>G (p.Glu637Gly) c.2006A>G (p.Glu669Gly) n.425A>G c.1967A>G (p.Glu656Gly) c.1799A>G (p.Glu600Gly) | ClinVar dbSNP |
| 21 | g.25891855T= | CA2383551644 | APP | n.2045A= n.475A= n.744A= c.2078A= (p.Glu693=) c.1853A= (p.Glu618=) c.1685A= (p.Glu562=) c.2021A= (p.Glu674=) c.2024A= (p.Glu675=) c.1748A= (p.Glu583=) c.1910A= (p.Glu637=) c.2006A= (p.Glu669=) n.425A= c.1967A= (p.Glu656=) c.1799A= (p.Glu600=) | dbSNP |