Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.121515280T>C | CA122987 | FGFR2 | c.1127A>G (p.Tyr376Cys) c.1124A>G (p.Tyr375Cys) c.-47A>G (n.-47A>G) n.472A>G c.779A>G (p.Tyr260Cys) c.404-11339A>G (n.404-11339A>G) n.3471A>G c.857A>G (p.Tyr286Cys) c.1130A>G (p.Tyr377Cys) c.860A>G (p.Tyr287Cys) c.782A>G (p.Tyr261Cys) c.939+4699A>G (n.939+4699A>G) c.788A>G (p.Tyr263Cys) n.333A>G c.440A>G (p.Tyr147Cys) c.*171A>G (n.*171A>G) n.1574A>G c.1184A>G (p.Tyr395Cys) c.1181A>G (p.Tyr394Cys) c.917A>G (p.Tyr306Cys) c.839A>G (p.Tyr280Cys) c.836A>G (p.Tyr279Cys) c.914A>G (p.Tyr305Cys) n.1560A>G | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
10 | g.121515280T>A | CA378327313 | FGFR2 | c.1127A>T (p.Tyr376Phe) c.1124A>T (p.Tyr375Phe) c.-47A>T (n.-47A>T) n.472A>T c.779A>T (p.Tyr260Phe) c.404-11339A>T (n.404-11339A>T) n.3471A>T c.857A>T (p.Tyr286Phe) c.1130A>T (p.Tyr377Phe) c.860A>T (p.Tyr287Phe) c.782A>T (p.Tyr261Phe) c.939+4699A>T (n.939+4699A>T) c.788A>T (p.Tyr263Phe) n.333A>T c.440A>T (p.Tyr147Phe) c.*171A>T (n.*171A>T) n.1574A>T c.1184A>T (p.Tyr395Phe) c.1181A>T (p.Tyr394Phe) c.917A>T (p.Tyr306Phe) c.839A>T (p.Tyr280Phe) c.836A>T (p.Tyr279Phe) c.914A>T (p.Tyr305Phe) n.1560A>T | ClinVar dbSNP |
10 | g.121515280T>G | CA378327315 | FGFR2 | c.1127A>C (p.Tyr376Ser) c.1124A>C (p.Tyr375Ser) c.-47A>C (n.-47A>C) n.472A>C c.779A>C (p.Tyr260Ser) c.404-11339A>C (n.404-11339A>C) n.3471A>C c.857A>C (p.Tyr286Ser) c.1130A>C (p.Tyr377Ser) c.860A>C (p.Tyr287Ser) c.782A>C (p.Tyr261Ser) c.939+4699A>C (n.939+4699A>C) c.788A>C (p.Tyr263Ser) n.333A>C c.440A>C (p.Tyr147Ser) c.*171A>C (n.*171A>C) n.1574A>C c.1184A>C (p.Tyr395Ser) c.1181A>C (p.Tyr394Ser) c.917A>C (p.Tyr306Ser) c.839A>C (p.Tyr280Ser) c.836A>C (p.Tyr279Ser) c.914A>C (p.Tyr305Ser) n.1560A>C | dbSNP |