| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.25891793T>C | CA127814 | APP | n.2107A>G n.537A>G n.806A>G c.2140A>G (p.Thr714Ala) c.1915A>G (p.Thr639Ala) c.1747A>G (p.Thr583Ala) c.2083A>G (p.Thr695Ala) c.2086A>G (p.Thr696Ala) c.1810A>G (p.Thr604Ala) c.1972A>G (p.Thr658Ala) c.2068A>G (p.Thr690Ala) n.487A>G c.2029A>G (p.Thr677Ala) c.1861A>G (p.Thr621Ala) | ClinVar dbSNP COSMIC |
| 21 | g.25891793T= | CA2383551619 | APP | n.2107A= n.537A= n.806A= c.2140A= (p.Thr714=) c.1915A= (p.Thr639=) c.1747A= (p.Thr583=) c.2083A= (p.Thr695=) c.2086A= (p.Thr696=) c.1810A= (p.Thr604=) c.1972A= (p.Thr658=) c.2068A= (p.Thr690=) n.487A= c.2029A= (p.Thr677=) c.1861A= (p.Thr621=) | dbSNP |