| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.148811635T>C | CA369713035 | EZH2 | n.3837A>G c.*999A>G (n.*999A>G) c.*833A>G (n.*833A>G) n.3656A>G n.2828A>G n.2253A>G n.2315A>G c.1937A>G (p.Tyr646Cys) c.1805A>G (p.Tyr602Cys) c.1922A>G (p.Tyr641Cys) n.189A>G c.1769A>G (p.Tyr590Cys) c.1895A>G (p.Tyr632Cys) c.*1927A>G (n.*1927A>G) c.1946A>G (p.Tyr649Cys) c.1919A>G (p.Tyr640Cys) c.1793A>G (p.Tyr598Cys) c.1961A>G (p.Tyr654Cys) c.1934A>G (p.Tyr645Cys) c.1913A>G (p.Tyr638Cys) c.1910A>G (p.Tyr637Cys) c.1871A>G (p.Tyr624Cys) c.1844A>G (p.Tyr615Cys) c.1838A>G (p.Tyr613Cys) c.1835A>G (p.Tyr612Cys) c.1829A>G (p.Tyr610Cys) c.1820A>G (p.Tyr607Cys) c.1817A>G (p.Tyr606Cys) c.1703A>G (p.Tyr568Cys) c.1610A>G (p.Tyr537Cys) n.515+6550T>C n.722+6550T>C c.1898A>G (p.Tyr633Cys) c.1595A>G (p.Tyr532Cys) c.1823A>G (p.Tyr608Cys) n.4311A>G n.4967A>G n.5427A>G | dbSNP COSMIC COSMIC |
| 7 | g.148811635T>G | CA16602671 | EZH2 | n.3837A>C c.*999A>C (n.*999A>C) c.*833A>C (n.*833A>C) n.3656A>C n.2828A>C n.2253A>C n.2315A>C c.1937A>C (p.Tyr646Ser) c.1805A>C (p.Tyr602Ser) c.1922A>C (p.Tyr641Ser) n.189A>C c.1769A>C (p.Tyr590Ser) c.1895A>C (p.Tyr632Ser) c.*1927A>C (n.*1927A>C) c.1946A>C (p.Tyr649Ser) c.1919A>C (p.Tyr640Ser) c.1793A>C (p.Tyr598Ser) c.1961A>C (p.Tyr654Ser) c.1934A>C (p.Tyr645Ser) c.1913A>C (p.Tyr638Ser) c.1910A>C (p.Tyr637Ser) c.1871A>C (p.Tyr624Ser) c.1844A>C (p.Tyr615Ser) c.1838A>C (p.Tyr613Ser) c.1835A>C (p.Tyr612Ser) c.1829A>C (p.Tyr610Ser) c.1820A>C (p.Tyr607Ser) c.1817A>C (p.Tyr606Ser) c.1703A>C (p.Tyr568Ser) c.1610A>C (p.Tyr537Ser) n.515+6550T>G n.722+6550T>G c.1898A>C (p.Tyr633Ser) c.1595A>C (p.Tyr532Ser) c.1823A>C (p.Tyr608Ser) n.4311A>C n.4967A>C n.5427A>C | ClinVar dbSNP COSMIC COSMIC |
| 7 | g.148811635T>A | CA16602259 | EZH2 | n.3837A>T c.*999A>T (n.*999A>T) c.*833A>T (n.*833A>T) n.3656A>T n.2828A>T n.2253A>T n.2315A>T c.1937A>T (p.Tyr646Phe) c.1805A>T (p.Tyr602Phe) c.1922A>T (p.Tyr641Phe) n.189A>T c.1769A>T (p.Tyr590Phe) c.1895A>T (p.Tyr632Phe) c.*1927A>T (n.*1927A>T) c.1946A>T (p.Tyr649Phe) c.1919A>T (p.Tyr640Phe) c.1793A>T (p.Tyr598Phe) c.1961A>T (p.Tyr654Phe) c.1934A>T (p.Tyr645Phe) c.1913A>T (p.Tyr638Phe) c.1910A>T (p.Tyr637Phe) c.1871A>T (p.Tyr624Phe) c.1844A>T (p.Tyr615Phe) c.1838A>T (p.Tyr613Phe) c.1835A>T (p.Tyr612Phe) c.1829A>T (p.Tyr610Phe) c.1820A>T (p.Tyr607Phe) c.1817A>T (p.Tyr606Phe) c.1703A>T (p.Tyr568Phe) c.1610A>T (p.Tyr537Phe) n.515+6550T>A n.722+6550T>A c.1898A>T (p.Tyr633Phe) c.1595A>T (p.Tyr532Phe) c.1823A>T (p.Tyr608Phe) n.4311A>T n.4967A>T n.5427A>T | ClinVar dbSNP COSMIC COSMIC |
| 7 | g.148811635T= | CA1751424143 | EZH2 | n.3837A= c.*999A= (n.*999A=) c.*833A= (n.*833A=) n.3656A= n.2828A= n.2253A= n.2315A= c.1937A= (p.Tyr646=) c.1805A= (p.Tyr602=) c.1922A= (p.Tyr641=) n.189A= c.1769A= (p.Tyr590=) c.1895A= (p.Tyr632=) c.*1927A= (n.*1927A=) c.1946A= (p.Tyr649=) c.1919A= (p.Tyr640=) c.1793A= (p.Tyr598=) c.1961A= (p.Tyr654=) c.1934A= (p.Tyr645=) c.1913A= (p.Tyr638=) c.1910A= (p.Tyr637=) c.1871A= (p.Tyr624=) c.1844A= (p.Tyr615=) c.1838A= (p.Tyr613=) c.1835A= (p.Tyr612=) c.1829A= (p.Tyr610=) c.1820A= (p.Tyr607=) c.1817A= (p.Tyr606=) c.1703A= (p.Tyr568=) c.1610A= (p.Tyr537=) n.515+6550T= n.722+6550T= c.1898A= (p.Tyr633=) c.1595A= (p.Tyr532=) c.1823A= (p.Tyr608=) n.4311A= n.4967A= n.5427A= | dbSNP |