| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.25891783A>C | CA127793 | APP | n.2117T>G n.547T>G n.816T>G c.2150T>G (p.Val717Gly) c.1925T>G (p.Val642Gly) c.1757T>G (p.Val586Gly) c.2093T>G (p.Val698Gly) c.2096T>G (p.Val699Gly) c.1820T>G (p.Val607Gly) c.1982T>G (p.Val661Gly) c.2078T>G (p.Val693Gly) n.497T>G c.2039T>G (p.Val680Gly) c.1871T>G (p.Val624Gly) | ClinVar dbSNP |
| 21 | g.25891783A= | CA2383551610 | APP | n.2117T= n.547T= n.816T= c.2150T= (p.Val717=) c.1925T= (p.Val642=) c.1757T= (p.Val586=) c.2093T= (p.Val698=) c.2096T= (p.Val699=) c.1820T= (p.Val607=) c.1982T= (p.Val661=) c.2078T= (p.Val693=) n.497T= c.2039T= (p.Val680=) c.1871T= (p.Val624=) | dbSNP |