Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.25897619G>A | CA258118 | APP | n.1985C>T n.415C>T n.684C>T c.2018C>T (p.Ala673Val) c.1793C>T (p.Ala598Val) c.1625C>T (p.Ala542Val) c.1961C>T (p.Ala654Val) c.1964C>T (p.Ala655Val) c.1688C>T (p.Ala563Val) c.1850C>T (p.Ala617Val) c.1946C>T (p.Ala649Val) n.365C>T c.1907C>T (p.Ala636Val) c.1739C>T (p.Ala580Val) | ClinVar dbSNP |
21 | g.25897619G>C | CA409806410 | APP | n.1985C>G n.415C>G n.684C>G c.2018C>G (p.Ala673Gly) c.1793C>G (p.Ala598Gly) c.1625C>G (p.Ala542Gly) c.1961C>G (p.Ala654Gly) c.1964C>G (p.Ala655Gly) c.1688C>G (p.Ala563Gly) c.1850C>G (p.Ala617Gly) c.1946C>G (p.Ala649Gly) n.365C>G c.1907C>G (p.Ala636Gly) c.1739C>G (p.Ala580Gly) | dbSNP |