Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121496701T>CCA16043906FGFR2c.1697A>G (p.Glu566Gly)
c.1688A>G (p.Glu563Gly)
c.518A>G (p.Glu173Gly)
n.1036A>G
c.1343A>G (p.Glu448Gly)
n.514A>G
n.106A>G
c.*396A>G (n.*396A>G)
n.4035A>G
n.2707A>G
c.1694A>G (p.Glu565Gly)
c.1421A>G (p.Glu474Gly)
c.1427A>G (p.Glu476Gly)
c.1430A>G (p.Glu477Gly)
c.1352A>G (p.Glu451Gly)
c.1346A>G (p.Glu449Gly)
c.1358A>G (p.Glu453Gly)
c.470A>G (p.Glu157Gly)
c.1010A>G (p.Glu337Gly)
c.*741A>G (n.*741A>G)
c.1349A>G (p.Glu450Gly)
n.2144A>G
c.1748A>G (p.Glu583Gly)
c.1745A>G (p.Glu582Gly)
c.1754A>G (p.Glu585Gly)
c.1487A>G (p.Glu496Gly)
c.1409A>G (p.Glu470Gly)
c.1751A>G (p.Glu584Gly)
c.1406A>G (p.Glu469Gly)
c.1400A>G (p.Glu467Gly)
c.1484A>G (p.Glu495Gly)
c.1481A>G (p.Glu494Gly)
c.1478A>G (p.Glu493Gly)
c.524A>G (p.Glu175Gly)
n.2130A>G
ClinVar dbSNP
10g.121496701T>GCA280192FGFR2c.1697A>C (p.Glu566Ala)
c.1688A>C (p.Glu563Ala)
c.518A>C (p.Glu173Ala)
n.1036A>C
c.1343A>C (p.Glu448Ala)
n.514A>C
n.106A>C
c.*396A>C (n.*396A>C)
n.4035A>C
n.2707A>C
c.1694A>C (p.Glu565Ala)
c.1421A>C (p.Glu474Ala)
c.1427A>C (p.Glu476Ala)
c.1430A>C (p.Glu477Ala)
c.1352A>C (p.Glu451Ala)
c.1346A>C (p.Glu449Ala)
c.1358A>C (p.Glu453Ala)
c.470A>C (p.Glu157Ala)
c.1010A>C (p.Glu337Ala)
c.*741A>C (n.*741A>C)
c.1349A>C (p.Glu450Ala)
n.2144A>C
c.1748A>C (p.Glu583Ala)
c.1745A>C (p.Glu582Ala)
c.1754A>C (p.Glu585Ala)
c.1487A>C (p.Glu496Ala)
c.1409A>C (p.Glu470Ala)
c.1751A>C (p.Glu584Ala)
c.1406A>C (p.Glu469Ala)
c.1400A>C (p.Glu467Ala)
c.1484A>C (p.Glu495Ala)
c.1481A>C (p.Glu494Ala)
c.1478A>C (p.Glu493Ala)
c.524A>C (p.Glu175Ala)
n.2130A>C
ClinVar dbSNP
10g.121496701T>ACA378320641FGFR2c.1697A>T (p.Glu566Val)
c.1688A>T (p.Glu563Val)
c.518A>T (p.Glu173Val)
n.1036A>T
c.1343A>T (p.Glu448Val)
n.514A>T
n.106A>T
c.*396A>T (n.*396A>T)
n.4035A>T
n.2707A>T
c.1694A>T (p.Glu565Val)
c.1421A>T (p.Glu474Val)
c.1427A>T (p.Glu476Val)
c.1430A>T (p.Glu477Val)
c.1352A>T (p.Glu451Val)
c.1346A>T (p.Glu449Val)
c.1358A>T (p.Glu453Val)
c.470A>T (p.Glu157Val)
c.1010A>T (p.Glu337Val)
c.*741A>T (n.*741A>T)
c.1349A>T (p.Glu450Val)
n.2144A>T
c.1748A>T (p.Glu583Val)
c.1745A>T (p.Glu582Val)
c.1754A>T (p.Glu585Val)
c.1487A>T (p.Glu496Val)
c.1409A>T (p.Glu470Val)
c.1751A>T (p.Glu584Val)
c.1406A>T (p.Glu469Val)
c.1400A>T (p.Glu467Val)
c.1484A>T (p.Glu495Val)
c.1481A>T (p.Glu494Val)
c.1478A>T (p.Glu493Val)
c.524A>T (p.Glu175Val)
n.2130A>T
dbSNP

Number of alleles fetched