| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.148811650T>G | CA16602850 | EZH2 | n.3822A>C c.*984A>C (n.*984A>C) c.*818A>C (n.*818A>C) n.3641A>C n.2813A>C n.2238A>C n.2300A>C c.1922A>C (p.Glu641Ala) c.1790A>C (p.Glu597Ala) c.1907A>C (p.Glu636Ala) n.174A>C c.1754A>C (p.Glu585Ala) c.1880A>C (p.Glu627Ala) c.*1912A>C (n.*1912A>C) c.1931A>C (p.Glu644Ala) c.1904A>C (p.Glu635Ala) c.1778A>C (p.Glu593Ala) c.1946A>C (p.Glu649Ala) c.1919A>C (p.Glu640Ala) c.1898A>C (p.Glu633Ala) c.1895A>C (p.Glu632Ala) c.1856A>C (p.Glu619Ala) c.1829A>C (p.Glu610Ala) c.1823A>C (p.Glu608Ala) c.1820A>C (p.Glu607Ala) c.1814A>C (p.Glu605Ala) c.1805A>C (p.Glu602Ala) c.1802A>C (p.Glu601Ala) c.1688A>C (p.Glu563Ala) c.1595A>C (p.Glu532Ala) n.515+6565T>G n.722+6565T>G c.1883A>C (p.Glu628Ala) c.1580A>C (p.Glu527Ala) c.1808A>C (p.Glu603Ala) n.4296A>C n.4952A>C n.5412A>C | ClinVar dbSNP |
| 7 | g.148811650T>A | CA16602849 | EZH2 | n.3822A>T c.*984A>T (n.*984A>T) c.*818A>T (n.*818A>T) n.3641A>T n.2813A>T n.2238A>T n.2300A>T c.1922A>T (p.Glu641Val) c.1790A>T (p.Glu597Val) c.1907A>T (p.Glu636Val) n.174A>T c.1754A>T (p.Glu585Val) c.1880A>T (p.Glu627Val) c.*1912A>T (n.*1912A>T) c.1931A>T (p.Glu644Val) c.1904A>T (p.Glu635Val) c.1778A>T (p.Glu593Val) c.1946A>T (p.Glu649Val) c.1919A>T (p.Glu640Val) c.1898A>T (p.Glu633Val) c.1895A>T (p.Glu632Val) c.1856A>T (p.Glu619Val) c.1829A>T (p.Glu610Val) c.1823A>T (p.Glu608Val) c.1820A>T (p.Glu607Val) c.1814A>T (p.Glu605Val) c.1805A>T (p.Glu602Val) c.1802A>T (p.Glu601Val) c.1688A>T (p.Glu563Val) c.1595A>T (p.Glu532Val) n.515+6565T>A n.722+6565T>A c.1883A>T (p.Glu628Val) c.1580A>T (p.Glu527Val) c.1808A>T (p.Glu603Val) n.4296A>T n.4952A>T n.5412A>T | ClinVar dbSNP COSMIC |