| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121498525T>G | CA16602868 | FGFR2 | c.1645A>C (p.Ile549Leu) c.1636A>C (p.Ile546Leu) c.466A>C (p.Ile156Leu) n.984A>C c.1291A>C (p.Ile431Leu) n.462A>C c.*344A>C (n.*344A>C) n.3983A>C n.2655A>C c.1642A>C (p.Ile548Leu) c.1369A>C (p.Ile457Leu) c.1375A>C (p.Ile459Leu) c.1378A>C (p.Ile460Leu) c.1300A>C (p.Ile434Leu) c.1294A>C (p.Ile432Leu) c.1306A>C (p.Ile436Leu) c.418A>C (p.Ile140Leu) c.958A>C (p.Ile320Leu) c.*689A>C (n.*689A>C) c.1297A>C (p.Ile433Leu) n.2092A>C c.1696A>C (p.Ile566Leu) c.1693A>C (p.Ile565Leu) c.1702A>C (p.Ile568Leu) c.1435A>C (p.Ile479Leu) c.1357A>C (p.Ile453Leu) c.1699A>C (p.Ile567Leu) c.1354A>C (p.Ile452Leu) c.1348A>C (p.Ile450Leu) c.1432A>C (p.Ile478Leu) c.1429A>C (p.Ile477Leu) c.1426A>C (p.Ile476Leu) c.472A>C (p.Ile158Leu) n.2078A>C | ClinVar dbSNP |
| 10 | g.121498525T>C | CA378321453 | FGFR2 | c.1645A>G (p.Ile549Val) c.1636A>G (p.Ile546Val) c.466A>G (p.Ile156Val) n.984A>G c.1291A>G (p.Ile431Val) n.462A>G c.*344A>G (n.*344A>G) n.3983A>G n.2655A>G c.1642A>G (p.Ile548Val) c.1369A>G (p.Ile457Val) c.1375A>G (p.Ile459Val) c.1378A>G (p.Ile460Val) c.1300A>G (p.Ile434Val) c.1294A>G (p.Ile432Val) c.1306A>G (p.Ile436Val) c.418A>G (p.Ile140Val) c.958A>G (p.Ile320Val) c.*689A>G (n.*689A>G) c.1297A>G (p.Ile433Val) n.2092A>G c.1696A>G (p.Ile566Val) c.1693A>G (p.Ile565Val) c.1702A>G (p.Ile568Val) c.1435A>G (p.Ile479Val) c.1357A>G (p.Ile453Val) c.1699A>G (p.Ile567Val) c.1354A>G (p.Ile452Val) c.1348A>G (p.Ile450Val) c.1432A>G (p.Ile478Val) c.1429A>G (p.Ile477Val) c.1426A>G (p.Ile476Val) c.472A>G (p.Ile158Val) n.2078A>G | dbSNP |