| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.42323046C>T | CA399582847 | STAT3 | c.1846G>A (p.Glu616Lys) c.*238G>A (n.*238G>A) c.1819G>A (p.Glu607Lys) n.1299G>A c.*234G>A (n.*234G>A) c.1942G>A (p.Glu648Lys) n.2046G>A c.1825G>A (p.Glu609Lys) c.1762G>A (p.Glu588Lys) c.1861G>A (p.Glu621Lys) n.2283G>A c.1750G>A (p.Glu584Lys) n.2263G>A n.2089G>A c.1552G>A (p.Glu518Lys) n.815G>A c.1768G>A (p.Glu590Lys) c.1786G>A (p.Glu596Lys) | dbSNP COSMIC |
| 17 | g.42323046C>A | CA399582844 | STAT3 | c.1846G>T (p.Glu616Ter) c.*238G>T (n.*238G>T) c.1819G>T (p.Glu607Ter) n.1299G>T c.*234G>T (n.*234G>T) c.1942G>T (p.Glu648Ter) n.2046G>T c.1825G>T (p.Glu609Ter) c.1762G>T (p.Glu588Ter) c.1861G>T (p.Glu621Ter) n.2283G>T c.1750G>T (p.Glu584Ter) n.2263G>T n.2089G>T c.1552G>T (p.Glu518Ter) n.815G>T c.1768G>T (p.Glu590Ter) c.1786G>T (p.Glu596Ter) | dbSNP |
| 17 | g.42323046C>G | CA16620411 | STAT3 | c.1846G>C (p.Glu616Gln) c.*238G>C (n.*238G>C) c.1819G>C (p.Glu607Gln) n.1299G>C c.*234G>C (n.*234G>C) c.1942G>C (p.Glu648Gln) n.2046G>C c.1825G>C (p.Glu609Gln) c.1762G>C (p.Glu588Gln) c.1861G>C (p.Glu621Gln) n.2283G>C c.1750G>C (p.Glu584Gln) n.2263G>C n.2089G>C c.1552G>C (p.Glu518Gln) n.815G>C c.1768G>C (p.Glu590Gln) c.1786G>C (p.Glu596Gln) | ClinVar dbSNP |
| 17 | g.42323046C= | CA2260430983 | STAT3 | c.1846G= (p.Glu616=) c.*238G= (n.*238G=) c.1819G= (p.Glu607=) n.1299G= c.*234G= (n.*234G=) c.1942G= (p.Glu648=) n.2046G= c.1825G= (p.Glu609=) c.1762G= (p.Glu588=) c.1861G= (p.Glu621=) n.2283G= c.1750G= (p.Glu584=) n.2263G= n.2089G= c.1552G= (p.Glu518=) n.815G= c.1768G= (p.Glu590=) c.1786G= (p.Glu596=) | dbSNP |