| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121498528T>C | CA16602615 | FGFR2 | c.1642A>G (p.Ile548Val) c.1633A>G (p.Ile545Val) c.463A>G (p.Ile155Val) n.981A>G c.1288A>G (p.Ile430Val) n.459A>G c.*341A>G (n.*341A>G) n.3980A>G n.2652A>G c.1639A>G (p.Ile547Val) c.1366A>G (p.Ile456Val) c.1372A>G (p.Ile458Val) c.1375A>G (p.Ile459Val) c.1297A>G (p.Ile433Val) c.1291A>G (p.Ile431Val) c.1303A>G (p.Ile435Val) c.415A>G (p.Ile139Val) c.955A>G (p.Ile319Val) c.*686A>G (n.*686A>G) c.1294A>G (p.Ile432Val) n.2089A>G c.1693A>G (p.Ile565Val) c.1690A>G (p.Ile564Val) c.1699A>G (p.Ile567Val) c.1432A>G (p.Ile478Val) c.1354A>G (p.Ile452Val) c.1696A>G (p.Ile566Val) c.1351A>G (p.Ile451Val) c.1345A>G (p.Ile449Val) c.1429A>G (p.Ile477Val) c.1426A>G (p.Ile476Val) c.1423A>G (p.Ile475Val) c.469A>G (p.Ile157Val) n.2075A>G | ClinVar dbSNP COSMIC |
| 10 | g.121498528T= | CA1941017706 | FGFR2 | c.1642A= (p.Ile548=) c.1633A= (p.Ile545=) c.463A= (p.Ile155=) n.981A= c.1288A= (p.Ile430=) n.459A= c.*341A= (n.*341A=) n.3980A= n.2652A= c.1639A= (p.Ile547=) c.1366A= (p.Ile456=) c.1372A= (p.Ile458=) c.1375A= (p.Ile459=) c.1297A= (p.Ile433=) c.1291A= (p.Ile431=) c.1303A= (p.Ile435=) c.415A= (p.Ile139=) c.955A= (p.Ile319=) c.*686A= (n.*686A=) c.1294A= (p.Ile432=) n.2089A= c.1693A= (p.Ile565=) c.1690A= (p.Ile564=) c.1699A= (p.Ile567=) c.1432A= (p.Ile478=) c.1354A= (p.Ile452=) c.1696A= (p.Ile566=) c.1351A= (p.Ile451=) c.1345A= (p.Ile449=) c.1429A= (p.Ile477=) c.1426A= (p.Ile476=) c.1423A= (p.Ile475=) c.469A= (p.Ile157=) n.2075A= | dbSNP |