| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121515283T>C | CA16603134 | FGFR2 | c.1124A>G (p.Asp375Gly) c.1121A>G (p.Asp374Gly) c.-50A>G (n.-50A>G) n.469A>G c.776A>G (p.Asp259Gly) c.404-11342A>G (n.404-11342A>G) n.3468A>G c.854A>G (p.Asp285Gly) c.1127A>G (p.Asp376Gly) c.857A>G (p.Asp286Gly) c.779A>G (p.Asp260Gly) c.939+4696A>G (n.939+4696A>G) c.785A>G (p.Asp262Gly) n.330A>G c.437A>G (p.Asp146Gly) c.*168A>G (n.*168A>G) n.1571A>G c.1181A>G (p.Asp394Gly) c.1178A>G (p.Asp393Gly) c.914A>G (p.Asp305Gly) c.836A>G (p.Asp279Gly) c.833A>G (p.Asp278Gly) c.911A>G (p.Asp304Gly) n.1557A>G | ClinVar dbSNP |
| 10 | g.121515283T>G | CA378327333 | FGFR2 | c.1124A>C (p.Asp375Ala) c.1121A>C (p.Asp374Ala) c.-50A>C (n.-50A>C) n.469A>C c.776A>C (p.Asp259Ala) c.404-11342A>C (n.404-11342A>C) n.3468A>C c.854A>C (p.Asp285Ala) c.1127A>C (p.Asp376Ala) c.857A>C (p.Asp286Ala) c.779A>C (p.Asp260Ala) c.939+4696A>C (n.939+4696A>C) c.785A>C (p.Asp262Ala) n.330A>C c.437A>C (p.Asp146Ala) c.*168A>C (n.*168A>C) n.1571A>C c.1181A>C (p.Asp394Ala) c.1178A>C (p.Asp393Ala) c.914A>C (p.Asp305Ala) c.836A>C (p.Asp279Ala) c.833A>C (p.Asp278Ala) c.911A>C (p.Asp304Ala) n.1557A>C | dbSNP |
| 10 | g.121515283T>A | CA378327328 | FGFR2 | c.1124A>T (p.Asp375Val) c.1121A>T (p.Asp374Val) c.-50A>T (n.-50A>T) n.469A>T c.776A>T (p.Asp259Val) c.404-11342A>T (n.404-11342A>T) n.3468A>T c.854A>T (p.Asp285Val) c.1127A>T (p.Asp376Val) c.857A>T (p.Asp286Val) c.779A>T (p.Asp260Val) c.939+4696A>T (n.939+4696A>T) c.785A>T (p.Asp262Val) n.330A>T c.437A>T (p.Asp146Val) c.*168A>T (n.*168A>T) n.1571A>T c.1181A>T (p.Asp394Val) c.1178A>T (p.Asp393Val) c.914A>T (p.Asp305Val) c.836A>T (p.Asp279Val) c.833A>T (p.Asp278Val) c.911A>T (p.Asp304Val) n.1557A>T | dbSNP |