Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121517378C>ACA16043909FGFR2c.1025G>T (p.Cys342Phe)
c.-146G>T (p.=)
n.373G>T
n.680G>T
c.680G>T (p.Cys227Phe)
c.404-13437G>T (p.=)
n.3372G>T
n.1025G>T
c.758G>T (p.Cys253Phe)
c.1031G>T (p.Cys344Phe)
c.820+1304G>T (p.=)
c.1087+1304G>T (p.=)
c.742+1304G>T (p.=)
c.939+2601G>T (p.=)
c.749-2059G>T (p.=)
n.234G>T
c.341G>T (p.Cys114Phe)
n.1434G>T
c.*72G>T (p.=)
n.1475G>T
c.1144+1304G>T (p.=)
c.1082G>T (p.Cys361Phe)
c.877+1304G>T (p.=)
c.799+1304G>T (p.=)
c.737G>T (p.Cys246Phe)
c.815G>T (p.Cys272Phe)
n.1461G>T
ClinVar dbSNP
10g.121517378C>GCA10575447FGFR2c.1025G>C (p.Cys342Ser)
c.-146G>C (p.=)
n.373G>C
n.680G>C
c.680G>C (p.Cys227Ser)
c.404-13437G>C (p.=)
n.3372G>C
n.1025G>C
c.758G>C (p.Cys253Ser)
c.1031G>C (p.Cys344Ser)
c.820+1304G>C (p.=)
c.1087+1304G>C (p.=)
c.742+1304G>C (p.=)
c.939+2601G>C (p.=)
c.749-2059G>C (p.=)
n.234G>C
c.341G>C (p.Cys114Ser)
n.1434G>C
c.*72G>C (p.=)
n.1475G>C
c.1144+1304G>C (p.=)
c.1082G>C (p.Cys361Ser)
c.877+1304G>C (p.=)
c.799+1304G>C (p.=)
c.737G>C (p.Cys246Ser)
c.815G>C (p.Cys272Ser)
n.1461G>C
ClinVar dbSNP
10g.121517378C>TCA280168FGFR2c.1025G>A (p.Cys342Tyr)
c.-146G>A (p.=)
n.373G>A
n.680G>A
c.680G>A (p.Cys227Tyr)
c.404-13437G>A (p.=)
n.3372G>A
n.1025G>A
c.758G>A (p.Cys253Tyr)
c.1031G>A (p.Cys344Tyr)
c.820+1304G>A (p.=)
c.1087+1304G>A (p.=)
c.742+1304G>A (p.=)
c.939+2601G>A (p.=)
c.749-2059G>A (p.=)
n.234G>A
c.341G>A (p.Cys114Tyr)
n.1434G>A
c.*72G>A (p.=)
n.1475G>A
c.1144+1304G>A (p.=)
c.1082G>A (p.Cys361Tyr)
c.877+1304G>A (p.=)
c.799+1304G>A (p.=)
c.737G>A (p.Cys246Tyr)
c.815G>A (p.Cys272Tyr)
n.1461G>A
ClinVar dbSNP

Number of alleles fetched