Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.42322474C>T | CA341510 | STAT3 | c.1909G>A (p.Val637Met) c.*301G>A (n.*301G>A) c.1882G>A (p.Val628Met) n.1362G>A c.*297G>A (n.*297G>A) c.2005G>A (p.Val669Met) n.2109G>A c.1888G>A (p.Val630Met) c.1825G>A (p.Val609Met) c.1924G>A (p.Val642Met) n.2346G>A c.1813G>A (p.Val605Met) n.2326G>A n.2152G>A c.1615G>A (p.Val539Met) c.1831G>A (p.Val611Met) c.1849G>A (p.Val617Met) | ClinVar dbSNP |
17 | g.42322474C>A | CA399582495 | STAT3 | c.1909G>T (p.Val637Leu) c.*301G>T (n.*301G>T) c.1882G>T (p.Val628Leu) n.1362G>T c.*297G>T (n.*297G>T) c.2005G>T (p.Val669Leu) n.2109G>T c.1888G>T (p.Val630Leu) c.1825G>T (p.Val609Leu) c.1924G>T (p.Val642Leu) n.2346G>T c.1813G>T (p.Val605Leu) n.2326G>T n.2152G>T c.1615G>T (p.Val539Leu) c.1831G>T (p.Val611Leu) c.1849G>T (p.Val617Leu) | ClinVar dbSNP |
17 | g.42322474C>G | CA399582497 | STAT3 | c.1909G>C (p.Val637Leu) c.*301G>C (n.*301G>C) c.1882G>C (p.Val628Leu) n.1362G>C c.*297G>C (n.*297G>C) c.2005G>C (p.Val669Leu) n.2109G>C c.1888G>C (p.Val630Leu) c.1825G>C (p.Val609Leu) c.1924G>C (p.Val642Leu) n.2346G>C c.1813G>C (p.Val605Leu) n.2326G>C n.2152G>C c.1615G>C (p.Val539Leu) c.1831G>C (p.Val611Leu) c.1849G>C (p.Val617Leu) | dbSNP |