Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121517386_121517392delCA645568650FGFR2c.1012_1018del (p.Gly338IlefsTer18)
c.745_751del (p.Gly249IlefsTer18)
c.1018_1024del (p.Gly340IlefsTer18)
c.667_673del (p.Gly223IlefsTer18)
c.820+1291_820+1297del (p.=)
c.1087+1291_1087+1297del (p.=)
c.742+1291_742+1297del (p.=)
c.939+2588_939+2594del (p.=)
c.749-2072_749-2066del (p.=)
n.221_227del
c.328_334del (p.Gly110IlefsTer18)
n.1421_1427del
c.*59_*65del (p.=)
n.1462_1468del
c.1144+1291_1144+1297del (p.=)
c.1069_1075del (p.Gly357IlefsTer18)
c.877+1291_877+1297del (p.=)
c.799+1291_799+1297del (p.=)
c.724_730del (p.Gly242IlefsTer18)
c.802_808del (p.Gly268IlefsTer18)
c.-159_-153del (p.=)
n.1448_1454del
COSMIC COSMIC COSMIC
10g.121517390_121517391delinsCCCA1941024611FGFR2c.1012_1013delinsGG (p.Gly338=)
c.745_746delinsGG (p.Gly249=)
c.1018_1019delinsGG (p.Gly340=)
c.667_668delinsGG (p.Gly223=)
c.820+1291_820+1292delinsGG (p.=)
c.1087+1291_1087+1292delinsGG (p.=)
c.742+1291_742+1292delinsGG (p.=)
c.939+2588_939+2589delinsGG (p.=)
c.749-2072_749-2071delinsGG (p.=)
n.221_222delinsGG
c.328_329delinsGG (p.Gly110=)
n.1421_1422delinsGG
c.*59_*60delinsGG (p.=)
n.1462_1463delinsGG
c.1144+1291_1144+1292delinsGG (p.=)
c.1069_1070delinsGG (p.Gly357=)
c.877+1291_877+1292delinsGG (p.=)
c.799+1291_799+1292delinsGG (p.=)
c.724_725delinsGG (p.Gly242=)
c.802_803delinsGG (p.Gly268=)
c.-159_-158delinsGG (p.=)
n.1448_1449delinsGG
10g.121517390_121517391delinsTTCA658658022FGFR2c.1012_1013delinsAA (p.Gly338Lys)
c.745_746delinsAA (p.Gly249Lys)
c.1018_1019delinsAA (p.Gly340Lys)
c.667_668delinsAA (p.Gly223Lys)
c.820+1291_820+1292delinsAA (p.=)
c.1087+1291_1087+1292delinsAA (p.=)
c.742+1291_742+1292delinsAA (p.=)
c.939+2588_939+2589delinsAA (p.=)
c.749-2072_749-2071delinsAA (p.=)
n.221_222delinsAA
c.328_329delinsAA (p.Gly110Lys)
n.1421_1422delinsAA
c.*59_*60delinsAA (p.=)
n.1462_1463delinsAA
c.1144+1291_1144+1292delinsAA (p.=)
c.1069_1070delinsAA (p.Gly357Lys)
c.877+1291_877+1292delinsAA (p.=)
c.799+1291_799+1292delinsAA (p.=)
c.724_725delinsAA (p.Gly242Lys)
c.802_803delinsAA (p.Gly268Lys)
c.-159_-158delinsAA (p.=)
n.1448_1449delinsAA
ClinVar dbSNP
10g.121517391C>ACA378328091FGFR2c.1012G>T (p.Gly338Trp)
c.745G>T (p.Gly249Trp)
c.1018G>T (p.Gly340Trp)
c.667G>T (p.Gly223Trp)
c.820+1291G>T (p.=)
c.1087+1291G>T (p.=)
c.742+1291G>T (p.=)
c.939+2588G>T (p.=)
c.749-2072G>T (p.=)
n.221G>T
c.328G>T (p.Gly110Trp)
n.1421G>T
c.*59G>T (p.=)
n.1462G>T
c.1144+1291G>T (p.=)
c.1069G>T (p.Gly357Trp)
c.877+1291G>T (p.=)
c.799+1291G>T (p.=)
c.724G>T (p.Gly242Trp)
c.802G>T (p.Gly268Trp)
c.-159G>T (p.=)
n.1448G>T
ClinVar
10g.121517391C=CA1941024612FGFR2c.1012G= (p.Gly338=)
c.745G= (p.Gly249=)
c.1018G= (p.Gly340=)
c.667G= (p.Gly223=)
c.820+1291G= (p.=)
c.1087+1291G= (p.=)
c.742+1291G= (p.=)
c.939+2588G= (p.=)
c.749-2072G= (p.=)
n.221G=
c.328G= (p.Gly110=)
n.1421G=
c.*59G= (p.=)
n.1462G=
c.1144+1291G= (p.=)
c.1069G= (p.Gly357=)
c.877+1291G= (p.=)
c.799+1291G= (p.=)
c.724G= (p.Gly242=)
c.802G= (p.Gly268=)
c.-159G= (p.=)
n.1448G=
10g.121517391C>GCA16043912FGFR2c.1012G>C (p.Gly338Arg)
c.745G>C (p.Gly249Arg)
c.1018G>C (p.Gly340Arg)
c.667G>C (p.Gly223Arg)
c.820+1291G>C (p.=)
c.1087+1291G>C (p.=)
c.742+1291G>C (p.=)
c.939+2588G>C (p.=)
c.749-2072G>C (p.=)
n.221G>C
c.328G>C (p.Gly110Arg)
n.1421G>C
c.*59G>C (p.=)
n.1462G>C
c.1144+1291G>C (p.=)
c.1069G>C (p.Gly357Arg)
c.877+1291G>C (p.=)
c.799+1291G>C (p.=)
c.724G>C (p.Gly242Arg)
c.802G>C (p.Gly268Arg)
c.-159G>C (p.=)
n.1448G>C
ClinVar
10g.121517391C>TCA378328094FGFR2c.1012G>A (p.Gly338Arg)
c.745G>A (p.Gly249Arg)
c.1018G>A (p.Gly340Arg)
c.667G>A (p.Gly223Arg)
c.820+1291G>A (p.=)
c.1087+1291G>A (p.=)
c.742+1291G>A (p.=)
c.939+2588G>A (p.=)
c.749-2072G>A (p.=)
n.221G>A
c.328G>A (p.Gly110Arg)
n.1421G>A
c.*59G>A (p.=)
n.1462G>A
c.1144+1291G>A (p.=)
c.1069G>A (p.Gly357Arg)
c.877+1291G>A (p.=)
c.799+1291G>A (p.=)
c.724G>A (p.Gly242Arg)
c.802G>A (p.Gly268Arg)
c.-159G>A (p.=)
n.1448G>A
ClinVar
10g.121517392A=CA1941024613FGFR2c.1011T= (p.Ala337=)
c.744T= (p.Ala248=)
c.1017T= (p.Ala339=)
c.666T= (p.Ala222=)
c.820+1290T= (p.=)
c.1087+1290T= (p.=)
c.742+1290T= (p.=)
c.939+2587T= (p.=)
c.749-2073T= (p.=)
n.220T=
c.327T= (p.Ala109=)
n.1420T=
c.*58T= (p.=)
n.1461T=
c.1144+1290T= (p.=)
c.1068T= (p.Ala356=)
c.877+1290T= (p.=)
c.799+1290T= (p.=)
c.723T= (p.Ala241=)
c.801T= (p.Ala267=)
c.-160T= (p.=)
n.1447T=
10g.121517392A>GCA10587075FGFR2c.1011T>C (p.Ala337=)
c.744T>C (p.Ala248=)
c.1017T>C (p.Ala339=)
c.666T>C (p.Ala222=)
c.820+1290T>C (p.=)
c.1087+1290T>C (p.=)
c.742+1290T>C (p.=)
c.939+2587T>C (p.=)
c.749-2073T>C (p.=)
n.220T>C
c.327T>C (p.Ala109=)
n.1420T>C
c.*58T>C (p.=)
n.1461T>C
c.1144+1290T>C (p.=)
c.1068T>C (p.Ala356=)
c.877+1290T>C (p.=)
c.799+1290T>C (p.=)
c.723T>C (p.Ala241=)
c.801T>C (p.Ala267=)
c.-160T>C (p.=)
n.1447T>C
ClinVar dbSNP
10g.121517393G>ACA378328099FGFR2c.1010C>T (p.Ala337Val)
c.743C>T (p.Ala248Val)
c.1016C>T (p.Ala339Val)
c.665C>T (p.Ala222Val)
c.820+1289C>T (p.=)
c.1087+1289C>T (p.=)
c.742+1289C>T (p.=)
c.939+2586C>T (p.=)
c.749-2074C>T (p.=)
n.219C>T
c.326C>T (p.Ala109Val)
n.1419C>T
c.*57C>T (p.=)
n.1460C>T
c.1144+1289C>T (p.=)
c.1067C>T (p.Ala356Val)
c.877+1289C>T (p.=)
c.799+1289C>T (p.=)
c.722C>T (p.Ala241Val)
c.800C>T (p.Ala267Val)
c.-161C>T (p.=)
n.1446C>T
COSMIC COSMIC COSMIC
10g.121517393G>CCA378328101FGFR2c.1010C>G (p.Ala337Gly)
c.743C>G (p.Ala248Gly)
c.1016C>G (p.Ala339Gly)
c.665C>G (p.Ala222Gly)
c.820+1289C>G (p.=)
c.1087+1289C>G (p.=)
c.742+1289C>G (p.=)
c.939+2586C>G (p.=)
c.749-2074C>G (p.=)
n.219C>G
c.326C>G (p.Ala109Gly)
n.1419C>G
c.*57C>G (p.=)
n.1460C>G
c.1144+1289C>G (p.=)
c.1067C>G (p.Ala356Gly)
c.877+1289C>G (p.=)
c.799+1289C>G (p.=)
c.722C>G (p.Ala241Gly)
c.800C>G (p.Ala267Gly)
c.-161C>G (p.=)
n.1446C>G
10g.121517393G>TCA378328103FGFR2c.1010C>A (p.Ala337Asp)
c.743C>A (p.Ala248Asp)
c.1016C>A (p.Ala339Asp)
c.665C>A (p.Ala222Asp)
c.820+1289C>A (p.=)
c.1087+1289C>A (p.=)
c.742+1289C>A (p.=)
c.939+2586C>A (p.=)
c.749-2074C>A (p.=)
n.219C>A
c.326C>A (p.Ala109Asp)
n.1419C>A
c.*57C>A (p.=)
n.1460C>A
c.1144+1289C>A (p.=)
c.1067C>A (p.Ala356Asp)
c.877+1289C>A (p.=)
c.799+1289C>A (p.=)
c.722C>A (p.Ala241Asp)
c.800C>A (p.Ala267Asp)
c.-161C>A (p.=)
n.1446C>A
10g.121517394C>ACA378328108FGFR2c.1009G>T (p.Ala337Ser)
c.742G>T (p.Ala248Ser)
c.1015G>T (p.Ala339Ser)
c.664G>T (p.Ala222Ser)
c.820+1288G>T (p.=)
c.1087+1288G>T (p.=)
c.742+1288G>T (p.=)
c.939+2585G>T (p.=)
c.749-2075G>T (p.=)
n.218G>T
c.325G>T (p.Ala109Ser)
n.1418G>T
c.*56G>T (p.=)
n.1459G>T
c.1144+1288G>T (p.=)
c.1066G>T (p.Ala356Ser)
c.877+1288G>T (p.=)
c.799+1288G>T (p.=)
c.721G>T (p.Ala241Ser)
c.799G>T (p.Ala267Ser)
c.-162G>T (p.=)
n.1445G>T
10g.121517394C=CA1941024614FGFR2c.1009G= (p.Ala337=)
c.742G= (p.Ala248=)
c.1015G= (p.Ala339=)
c.664G= (p.Ala222=)
c.820+1288G= (p.=)
c.1087+1288G= (p.=)
c.742+1288G= (p.=)
c.939+2585G= (p.=)
c.749-2075G= (p.=)
n.218G=
c.325G= (p.Ala109=)
n.1418G=
c.*56G= (p.=)
n.1459G=
c.1144+1288G= (p.=)
c.1066G= (p.Ala356=)
c.877+1288G= (p.=)
c.799+1288G= (p.=)
c.721G= (p.Ala241=)
c.799G= (p.Ala267=)
c.-162G= (p.=)
n.1445G=
10g.121517394C>GCA280240FGFR2c.1009G>C (p.Ala337Pro)
c.742G>C (p.Ala248Pro)
c.1015G>C (p.Ala339Pro)
c.664G>C (p.Ala222Pro)
c.820+1288G>C (p.=)
c.1087+1288G>C (p.=)
c.742+1288G>C (p.=)
c.939+2585G>C (p.=)
c.749-2075G>C (p.=)
n.218G>C
c.325G>C (p.Ala109Pro)
n.1418G>C
c.*56G>C (p.=)
n.1459G>C
c.1144+1288G>C (p.=)
c.1066G>C (p.Ala356Pro)
c.877+1288G>C (p.=)
c.799+1288G>C (p.=)
c.721G>C (p.Ala241Pro)
c.799G>C (p.Ala267Pro)
c.-162G>C (p.=)
n.1445G>C
ClinVar dbSNP
10g.121517394C>TCA128691FGFR2c.1009G>A (p.Ala337Thr)
c.742G>A (p.Ala248Thr)
c.1015G>A (p.Ala339Thr)
c.664G>A (p.Ala222Thr)
c.820+1288G>A (p.=)
c.1087+1288G>A (p.=)
c.742+1288G>A (p.=)
c.939+2585G>A (p.=)
c.749-2075G>A (p.=)
n.218G>A
c.325G>A (p.Ala109Thr)
n.1418G>A
c.*56G>A (p.=)
n.1459G>A
c.1144+1288G>A (p.=)
c.1066G>A (p.Ala356Thr)
c.877+1288G>A (p.=)
c.799+1288G>A (p.=)
c.721G>A (p.Ala241Thr)
c.799G>A (p.Ala267Thr)
c.-162G>A (p.=)
n.1445G>A
ClinVar dbSNP
10g.121517395G>ACA5720878FGFR2c.1008C>T (p.Asp336=)
c.741C>T (p.Asp247=)
c.1014C>T (p.Asp338=)
c.663C>T (p.Asp221=)
c.820+1287C>T (p.=)
c.1087+1287C>T (p.=)
c.742+1287C>T (p.=)
c.939+2584C>T (p.=)
c.749-2076C>T (p.=)
n.217C>T
c.324C>T (p.Asp108=)
n.1417C>T
c.*55C>T (p.=)
n.1458C>T
c.1144+1287C>T (p.=)
c.1065C>T (p.Asp355=)
c.877+1287C>T (p.=)
c.799+1287C>T (p.=)
c.720C>T (p.Asp240=)
c.798C>T (p.Asp266=)
c.-163C>T (p.=)
n.1444C>T
dbSNP ExAC gnomAD
10g.121517395G>CCA378328119FGFR2c.1008C>G (p.Asp336Glu)
c.741C>G (p.Asp247Glu)
c.1014C>G (p.Asp338Glu)
c.663C>G (p.Asp221Glu)
c.820+1287C>G (p.=)
c.1087+1287C>G (p.=)
c.742+1287C>G (p.=)
c.939+2584C>G (p.=)
c.749-2076C>G (p.=)
n.217C>G
c.324C>G (p.Asp108Glu)
n.1417C>G
c.*55C>G (p.=)
n.1458C>G
c.1144+1287C>G (p.=)
c.1065C>G (p.Asp355Glu)
c.877+1287C>G (p.=)
c.799+1287C>G (p.=)
c.720C>G (p.Asp240Glu)
c.798C>G (p.Asp266Glu)
c.-163C>G (p.=)
n.1444C>G
10g.121517395G=CA1941024615FGFR2c.1008C= (p.Asp336=)
c.741C= (p.Asp247=)
c.1014C= (p.Asp338=)
c.663C= (p.Asp221=)
c.820+1287C= (p.=)
c.1087+1287C= (p.=)
c.742+1287C= (p.=)
c.939+2584C= (p.=)
c.749-2076C= (p.=)
n.217C=
c.324C= (p.Asp108=)
n.1417C=
c.*55C= (p.=)
n.1458C=
c.1144+1287C= (p.=)
c.1065C= (p.Asp355=)
c.877+1287C= (p.=)
c.799+1287C= (p.=)
c.720C= (p.Asp240=)
c.798C= (p.Asp266=)
c.-163C= (p.=)
n.1444C=
10g.121517395G>TCA378328122FGFR2c.1008C>A (p.Asp336Glu)
c.741C>A (p.Asp247Glu)
c.1014C>A (p.Asp338Glu)
c.663C>A (p.Asp221Glu)
c.820+1287C>A (p.=)
c.1087+1287C>A (p.=)
c.742+1287C>A (p.=)
c.939+2584C>A (p.=)
c.749-2076C>A (p.=)
n.217C>A
c.324C>A (p.Asp108Glu)
n.1417C>A
c.*55C>A (p.=)
n.1458C>A
c.1144+1287C>A (p.=)
c.1065C>A (p.Asp355Glu)
c.877+1287C>A (p.=)
c.799+1287C>A (p.=)
c.720C>A (p.Asp240Glu)
c.798C>A (p.Asp266Glu)
c.-163C>A (p.=)
n.1444C>A
10g.121517396T>ACA378328124FGFR2c.1007A>T (p.Asp336Val)
c.740A>T (p.Asp247Val)
c.1013A>T (p.Asp338Val)
c.662A>T (p.Asp221Val)
c.820+1286A>T (p.=)
c.1087+1286A>T (p.=)
c.742+1286A>T (p.=)
c.939+2583A>T (p.=)
c.749-2077A>T (p.=)
n.216A>T
c.323A>T (p.Asp108Val)
n.1416A>T
c.*54A>T (p.=)
n.1457A>T
c.1144+1286A>T (p.=)
c.1064A>T (p.Asp355Val)
c.877+1286A>T (p.=)
c.799+1286A>T (p.=)
c.719A>T (p.Asp240Val)
c.797A>T (p.Asp266Val)
c.-164A>T (p.=)
n.1443A>T
10g.121517396T>CCA16043913FGFR2c.1007A>G (p.Asp336Gly)
c.740A>G (p.Asp247Gly)
c.1013A>G (p.Asp338Gly)
c.662A>G (p.Asp221Gly)
c.820+1286A>G (p.=)
c.1087+1286A>G (p.=)
c.742+1286A>G (p.=)
c.939+2583A>G (p.=)
c.749-2077A>G (p.=)
n.216A>G
c.323A>G (p.Asp108Gly)
n.1416A>G
c.*54A>G (p.=)
n.1457A>G
c.1144+1286A>G (p.=)
c.1064A>G (p.Asp355Gly)
c.877+1286A>G (p.=)
c.799+1286A>G (p.=)
c.719A>G (p.Asp240Gly)
c.797A>G (p.Asp266Gly)
c.-164A>G (p.=)
n.1443A>G
ClinVar
10g.121517396T>GCA378328128FGFR2c.1007A>C (p.Asp336Ala)
c.740A>C (p.Asp247Ala)
c.1013A>C (p.Asp338Ala)
c.662A>C (p.Asp221Ala)
c.820+1286A>C (p.=)
c.1087+1286A>C (p.=)
c.742+1286A>C (p.=)
c.939+2583A>C (p.=)
c.749-2077A>C (p.=)
n.216A>C
c.323A>C (p.Asp108Ala)
n.1416A>C
c.*54A>C (p.=)
n.1457A>C
c.1144+1286A>C (p.=)
c.1064A>C (p.Asp355Ala)
c.877+1286A>C (p.=)
c.799+1286A>C (p.=)
c.719A>C (p.Asp240Ala)
c.797A>C (p.Asp266Ala)
c.-164A>C (p.=)
n.1443A>C
10g.121517396T=CA1941024616FGFR2c.1007A= (p.Asp336=)
c.740A= (p.Asp247=)
c.1013A= (p.Asp338=)
c.662A= (p.Asp221=)
c.820+1286A= (p.=)
c.1087+1286A= (p.=)
c.742+1286A= (p.=)
c.939+2583A= (p.=)
c.749-2077A= (p.=)
n.216A=
c.323A= (p.Asp108=)
n.1416A=
c.*54A= (p.=)
n.1457A=
c.1144+1286A= (p.=)
c.1064A= (p.Asp355=)
c.877+1286A= (p.=)
c.799+1286A= (p.=)
c.719A= (p.Asp240=)
c.797A= (p.Asp266=)
c.-164A= (p.=)
n.1443A=
10g.121517397C>ACA378328131FGFR2c.1006G>T (p.Asp336Tyr)
c.739G>T (p.Asp247Tyr)
c.1012G>T (p.Asp338Tyr)
c.661G>T (p.Asp221Tyr)
c.820+1285G>T (p.=)
c.1087+1285G>T (p.=)
c.742+1285G>T (p.=)
c.939+2582G>T (p.=)
c.749-2078G>T (p.=)
n.215G>T
c.322G>T (p.Asp108Tyr)
n.1415G>T
c.*53G>T (p.=)
n.1456G>T
c.1144+1285G>T (p.=)
c.1063G>T (p.Asp355Tyr)
c.877+1285G>T (p.=)
c.799+1285G>T (p.=)
c.718G>T (p.Asp240Tyr)
c.796G>T (p.Asp266Tyr)
c.-165G>T (p.=)
n.1442G>T
10g.121517397C>GCA378328132FGFR2c.1006G>C (p.Asp336His)
c.739G>C (p.Asp247His)
c.1012G>C (p.Asp338His)
c.661G>C (p.Asp221His)
c.820+1285G>C (p.=)
c.1087+1285G>C (p.=)
c.742+1285G>C (p.=)
c.939+2582G>C (p.=)
c.749-2078G>C (p.=)
n.215G>C
c.322G>C (p.Asp108His)
n.1415G>C
c.*53G>C (p.=)
n.1456G>C
c.1144+1285G>C (p.=)
c.1063G>C (p.Asp355His)
c.877+1285G>C (p.=)
c.799+1285G>C (p.=)
c.718G>C (p.Asp240His)
c.796G>C (p.Asp266His)
c.-165G>C (p.=)
n.1442G>C
10g.121517397C>TCA378328133FGFR2c.1006G>A (p.Asp336Asn)
c.739G>A (p.Asp247Asn)
c.1012G>A (p.Asp338Asn)
c.661G>A (p.Asp221Asn)
c.820+1285G>A (p.=)
c.1087+1285G>A (p.=)
c.742+1285G>A (p.=)
c.939+2582G>A (p.=)
c.749-2078G>A (p.=)
n.215G>A
c.322G>A (p.Asp108Asn)
n.1415G>A
c.*53G>A (p.=)
n.1456G>A
c.1144+1285G>A (p.=)
c.1063G>A (p.Asp355Asn)
c.877+1285G>A (p.=)
c.799+1285G>A (p.=)
c.718G>A (p.Asp240Asn)
c.796G>A (p.Asp266Asn)
c.-165G>A (p.=)
n.1442G>A
10g.121517398C>ACA378328135FGFR2c.1005G>T (p.Glu335Asp)
c.738G>T (p.Glu246Asp)
c.1011G>T (p.Glu337Asp)
c.660G>T (p.Glu220Asp)
c.820+1284G>T (p.=)
c.1087+1284G>T (p.=)
c.742+1284G>T (p.=)
c.939+2581G>T (p.=)
c.749-2079G>T (p.=)
n.214G>T
c.321G>T (p.Glu107Asp)
n.1414G>T
c.*52G>T (p.=)
n.1455G>T
c.1144+1284G>T (p.=)
c.1062G>T (p.Glu354Asp)
c.877+1284G>T (p.=)
c.799+1284G>T (p.=)
c.717G>T (p.Glu239Asp)
c.795G>T (p.Glu265Asp)
c.-166G>T (p.=)
n.1441G>T
COSMIC COSMIC COSMIC
10g.121517398C>GCA378328139FGFR2c.1005G>C (p.Glu335Asp)
c.738G>C (p.Glu246Asp)
c.1011G>C (p.Glu337Asp)
c.660G>C (p.Glu220Asp)
c.820+1284G>C (p.=)
c.1087+1284G>C (p.=)
c.742+1284G>C (p.=)
c.939+2581G>C (p.=)
c.749-2079G>C (p.=)
n.214G>C
c.321G>C (p.Glu107Asp)
n.1414G>C
c.*52G>C (p.=)
n.1455G>C
c.1144+1284G>C (p.=)
c.1062G>C (p.Glu354Asp)
c.877+1284G>C (p.=)
c.799+1284G>C (p.=)
c.717G>C (p.Glu239Asp)
c.795G>C (p.Glu265Asp)
c.-166G>C (p.=)
n.1441G>C
10g.121517399T>ACA378328152FGFR2c.1004A>T (p.Glu335Val)
c.737A>T (p.Glu246Val)
c.1010A>T (p.Glu337Val)
c.659A>T (p.Glu220Val)
c.820+1283A>T (p.=)
c.1087+1283A>T (p.=)
c.742+1283A>T (p.=)
c.939+2580A>T (p.=)
c.749-2080A>T (p.=)
n.213A>T
c.320A>T (p.Glu107Val)
n.1413A>T
c.*51A>T (p.=)
n.1454A>T
c.1144+1283A>T (p.=)
c.1061A>T (p.Glu354Val)
c.877+1283A>T (p.=)
c.799+1283A>T (p.=)
c.716A>T (p.Glu239Val)
c.794A>T (p.Glu265Val)
c.-167A>T (p.=)
n.1440A>T
10g.121517399T>CCA378328149FGFR2c.1004A>G (p.Glu335Gly)
c.737A>G (p.Glu246Gly)
c.1010A>G (p.Glu337Gly)
c.659A>G (p.Glu220Gly)
c.820+1283A>G (p.=)
c.1087+1283A>G (p.=)
c.742+1283A>G (p.=)
c.939+2580A>G (p.=)
c.749-2080A>G (p.=)
n.213A>G
c.320A>G (p.Glu107Gly)
n.1413A>G
c.*51A>G (p.=)
n.1454A>G
c.1144+1283A>G (p.=)
c.1061A>G (p.Glu354Gly)
c.877+1283A>G (p.=)
c.799+1283A>G (p.=)
c.716A>G (p.Glu239Gly)
c.794A>G (p.Glu265Gly)
c.-167A>G (p.=)
n.1440A>G
10g.121517399T>GCA378328143FGFR2c.1004A>C (p.Glu335Ala)
c.737A>C (p.Glu246Ala)
c.1010A>C (p.Glu337Ala)
c.659A>C (p.Glu220Ala)
c.820+1283A>C (p.=)
c.1087+1283A>C (p.=)
c.742+1283A>C (p.=)
c.939+2580A>C (p.=)
c.749-2080A>C (p.=)
n.213A>C
c.320A>C (p.Glu107Ala)
n.1413A>C
c.*51A>C (p.=)
n.1454A>C
c.1144+1283A>C (p.=)
c.1061A>C (p.Glu354Ala)
c.877+1283A>C (p.=)
c.799+1283A>C (p.=)
c.716A>C (p.Glu239Ala)
c.794A>C (p.Glu265Ala)
c.-167A>C (p.=)
n.1440A>C
10g.121517400C>ACA378328156FGFR2c.1003G>T (p.Glu335Ter)
c.736G>T (p.Glu246Ter)
c.1009G>T (p.Glu337Ter)
c.658G>T (p.Glu220Ter)
c.820+1282G>T (p.=)
c.1087+1282G>T (p.=)
c.742+1282G>T (p.=)
c.939+2579G>T (p.=)
c.749-2081G>T (p.=)
n.212G>T
c.319G>T (p.Glu107Ter)
n.1412G>T
c.*50G>T (p.=)
n.1453G>T
c.1144+1282G>T (p.=)
c.1060G>T (p.Glu354Ter)
c.877+1282G>T (p.=)
c.799+1282G>T (p.=)
c.715G>T (p.Glu239Ter)
c.793G>T (p.Glu265Ter)
c.-168G>T (p.=)
n.1439G>T
10g.121517400C>GCA378328162FGFR2c.1003G>C (p.Glu335Gln)
c.736G>C (p.Glu246Gln)
c.1009G>C (p.Glu337Gln)
c.658G>C (p.Glu220Gln)
c.820+1282G>C (p.=)
c.1087+1282G>C (p.=)
c.742+1282G>C (p.=)
c.939+2579G>C (p.=)
c.749-2081G>C (p.=)
n.212G>C
c.319G>C (p.Glu107Gln)
n.1412G>C
c.*50G>C (p.=)
n.1453G>C
c.1144+1282G>C (p.=)
c.1060G>C (p.Glu354Gln)
c.877+1282G>C (p.=)
c.799+1282G>C (p.=)
c.715G>C (p.Glu239Gln)
c.793G>C (p.Glu265Gln)
c.-168G>C (p.=)
n.1439G>C
10g.121517400C>TCA378328159FGFR2c.1003G>A (p.Glu335Lys)
c.736G>A (p.Glu246Lys)
c.1009G>A (p.Glu337Lys)
c.658G>A (p.Glu220Lys)
c.820+1282G>A (p.=)
c.1087+1282G>A (p.=)
c.742+1282G>A (p.=)
c.939+2579G>A (p.=)
c.749-2081G>A (p.=)
n.212G>A
c.319G>A (p.Glu107Lys)
n.1412G>A
c.*50G>A (p.=)
n.1453G>A
c.1144+1282G>A (p.=)
c.1060G>A (p.Glu354Lys)
c.877+1282G>A (p.=)
c.799+1282G>A (p.=)
c.715G>A (p.Glu239Lys)
c.793G>A (p.Glu265Lys)
c.-168G>A (p.=)
n.1439G>A
10g.121517401A=CA1941024617FGFR2c.1002T= (p.Phe334=)
c.735T= (p.Phe245=)
c.1008T= (p.Phe336=)
c.657T= (p.Phe219=)
c.820+1281T= (p.=)
c.1087+1281T= (p.=)
c.742+1281T= (p.=)
c.939+2578T= (p.=)
c.749-2082T= (p.=)
n.211T=
c.318T= (p.Phe106=)
n.1411T=
c.*49T= (p.=)
n.1452T=
c.1144+1281T= (p.=)
c.1059T= (p.Phe353=)
c.877+1281T= (p.=)
c.799+1281T= (p.=)
c.714T= (p.Phe238=)
c.792T= (p.Phe264=)
c.-169T= (p.=)
n.1438T=
10g.121517401A>CCA378328165FGFR2c.1002T>G (p.Phe334Leu)
c.735T>G (p.Phe245Leu)
c.1008T>G (p.Phe336Leu)
c.657T>G (p.Phe219Leu)
c.820+1281T>G (p.=)
c.1087+1281T>G (p.=)
c.742+1281T>G (p.=)
c.939+2578T>G (p.=)
c.749-2082T>G (p.=)
n.211T>G
c.318T>G (p.Phe106Leu)
n.1411T>G
c.*49T>G (p.=)
n.1452T>G
c.1144+1281T>G (p.=)
c.1059T>G (p.Phe353Leu)
c.877+1281T>G (p.=)
c.799+1281T>G (p.=)
c.714T>G (p.Phe238Leu)
c.792T>G (p.Phe264Leu)
c.-169T>G (p.=)
n.1438T>G
10g.121517401A>GCA214310228FGFR2c.1002T>C (p.Phe334=)
c.735T>C (p.Phe245=)
c.1008T>C (p.Phe336=)
c.657T>C (p.Phe219=)
c.820+1281T>C (p.=)
c.1087+1281T>C (p.=)
c.742+1281T>C (p.=)
c.939+2578T>C (p.=)
c.749-2082T>C (p.=)
n.211T>C
c.318T>C (p.Phe106=)
n.1411T>C
c.*49T>C (p.=)
n.1452T>C
c.1144+1281T>C (p.=)
c.1059T>C (p.Phe353=)
c.877+1281T>C (p.=)
c.799+1281T>C (p.=)
c.714T>C (p.Phe238=)
c.792T>C (p.Phe264=)
c.-169T>C (p.=)
n.1438T>C
dbSNP gnomAD
10g.121517401A>TCA378328166FGFR2c.1002T>A (p.Phe334Leu)
c.735T>A (p.Phe245Leu)
c.1008T>A (p.Phe336Leu)
c.657T>A (p.Phe219Leu)
c.820+1281T>A (p.=)
c.1087+1281T>A (p.=)
c.742+1281T>A (p.=)
c.939+2578T>A (p.=)
c.749-2082T>A (p.=)
n.211T>A
c.318T>A (p.Phe106Leu)
n.1411T>A
c.*49T>A (p.=)
n.1452T>A
c.1144+1281T>A (p.=)
c.1059T>A (p.Phe353Leu)
c.877+1281T>A (p.=)
c.799+1281T>A (p.=)
c.714T>A (p.Phe238Leu)
c.792T>A (p.Phe264Leu)
c.-169T>A (p.=)
n.1438T>A
10g.121517402A=CA1941024618FGFR2c.1001T= (p.Phe334=)
c.734T= (p.Phe245=)
c.1007T= (p.Phe336=)
c.656T= (p.Phe219=)
c.820+1280T= (p.=)
c.1087+1280T= (p.=)
c.742+1280T= (p.=)
c.939+2577T= (p.=)
c.749-2083T= (p.=)
n.210T=
c.317T= (p.Phe106=)
n.1410T=
c.*48T= (p.=)
n.1451T=
c.1144+1280T= (p.=)
c.1058T= (p.Phe353=)
c.877+1280T= (p.=)
c.799+1280T= (p.=)
c.713T= (p.Phe238=)
c.791T= (p.Phe264=)
c.-170T= (p.=)
n.1437T=
10g.121517402A>CCA378328168FGFR2c.1001T>G (p.Phe334Cys)
c.734T>G (p.Phe245Cys)
c.1007T>G (p.Phe336Cys)
c.656T>G (p.Phe219Cys)
c.820+1280T>G (p.=)
c.1087+1280T>G (p.=)
c.742+1280T>G (p.=)
c.939+2577T>G (p.=)
c.749-2083T>G (p.=)
n.210T>G
c.317T>G (p.Phe106Cys)
n.1410T>G
c.*48T>G (p.=)
n.1451T>G
c.1144+1280T>G (p.=)
c.1058T>G (p.Phe353Cys)
c.877+1280T>G (p.=)
c.799+1280T>G (p.=)
c.713T>G (p.Phe238Cys)
c.791T>G (p.Phe264Cys)
c.-170T>G (p.=)
n.1437T>G
10g.121517402A>GCA378328170FGFR2c.1001T>C (p.Phe334Ser)
c.734T>C (p.Phe245Ser)
c.1007T>C (p.Phe336Ser)
c.656T>C (p.Phe219Ser)
c.820+1280T>C (p.=)
c.1087+1280T>C (p.=)
c.742+1280T>C (p.=)
c.939+2577T>C (p.=)
c.749-2083T>C (p.=)
n.210T>C
c.317T>C (p.Phe106Ser)
n.1410T>C
c.*48T>C (p.=)
n.1451T>C
c.1144+1280T>C (p.=)
c.1058T>C (p.Phe353Ser)
c.877+1280T>C (p.=)
c.799+1280T>C (p.=)
c.713T>C (p.Phe238Ser)
c.791T>C (p.Phe264Ser)
c.-170T>C (p.=)
n.1437T>C
10g.121517402A>TCA5720879FGFR2c.1001T>A (p.Phe334Tyr)
c.734T>A (p.Phe245Tyr)
c.1007T>A (p.Phe336Tyr)
c.656T>A (p.Phe219Tyr)
c.820+1280T>A (p.=)
c.1087+1280T>A (p.=)
c.742+1280T>A (p.=)
c.939+2577T>A (p.=)
c.749-2083T>A (p.=)
n.210T>A
c.317T>A (p.Phe106Tyr)
n.1410T>A
c.*48T>A (p.=)
n.1451T>A
c.1144+1280T>A (p.=)
c.1058T>A (p.Phe353Tyr)
c.877+1280T>A (p.=)
c.799+1280T>A (p.=)
c.713T>A (p.Phe238Tyr)
c.791T>A (p.Phe264Tyr)
c.-170T>A (p.=)
n.1437T>A
dbSNP ExAC gnomAD
10g.121517403A>CCA378328179FGFR2c.1000T>G (p.Phe334Val)
c.733T>G (p.Phe245Val)
c.1006T>G (p.Phe336Val)
c.655T>G (p.Phe219Val)
c.820+1279T>G (p.=)
c.1087+1279T>G (p.=)
c.742+1279T>G (p.=)
c.939+2576T>G (p.=)
c.749-2084T>G (p.=)
n.209T>G
c.316T>G (p.Phe106Val)
n.1409T>G
c.*47T>G (p.=)
n.1450T>G
c.1144+1279T>G (p.=)
c.1057T>G (p.Phe353Val)
c.877+1279T>G (p.=)
c.799+1279T>G (p.=)
c.712T>G (p.Phe238Val)
c.790T>G (p.Phe264Val)
c.-171T>G (p.=)
n.1436T>G
10g.121517403A>GCA378328180FGFR2c.1000T>C (p.Phe334Leu)
c.733T>C (p.Phe245Leu)
c.1006T>C (p.Phe336Leu)
c.655T>C (p.Phe219Leu)
c.820+1279T>C (p.=)
c.1087+1279T>C (p.=)
c.742+1279T>C (p.=)
c.939+2576T>C (p.=)
c.749-2084T>C (p.=)
n.209T>C
c.316T>C (p.Phe106Leu)
n.1409T>C
c.*47T>C (p.=)
n.1450T>C
c.1144+1279T>C (p.=)
c.1057T>C (p.Phe353Leu)
c.877+1279T>C (p.=)
c.799+1279T>C (p.=)
c.712T>C (p.Phe238Leu)
c.790T>C (p.Phe264Leu)
c.-171T>C (p.=)
n.1436T>C
10g.121517403A>TCA378328184FGFR2c.1000T>A (p.Phe334Ile)
c.733T>A (p.Phe245Ile)
c.1006T>A (p.Phe336Ile)
c.655T>A (p.Phe219Ile)
c.820+1279T>A (p.=)
c.1087+1279T>A (p.=)
c.742+1279T>A (p.=)
c.939+2576T>A (p.=)
c.749-2084T>A (p.=)
n.209T>A
c.316T>A (p.Phe106Ile)
n.1409T>A
c.*47T>A (p.=)
n.1450T>A
c.1144+1279T>A (p.=)
c.1057T>A (p.Phe353Ile)
c.877+1279T>A (p.=)
c.799+1279T>A (p.=)
c.712T>A (p.Phe238Ile)
c.790T>A (p.Phe264Ile)
c.-171T>A (p.=)
n.1436T>A
10g.121517405G>ACA378328189FGFR2c.998C>T (p.Thr333Ile)
c.731C>T (p.Thr244Ile)
c.1004C>T (p.Thr335Ile)
c.653C>T (p.Thr218Ile)
c.820+1277C>T (p.=)
c.1087+1277C>T (p.=)
c.742+1277C>T (p.=)
c.939+2574C>T (p.=)
c.749-2086C>T (p.=)
n.207C>T
c.314C>T (p.Thr105Ile)
n.1407C>T
c.*45C>T (p.=)
n.1448C>T
c.1144+1277C>T (p.=)
c.1055C>T (p.Thr352Ile)
c.877+1277C>T (p.=)
c.799+1277C>T (p.=)
c.710C>T (p.Thr237Ile)
c.788C>T (p.Thr263Ile)
c.-173C>T (p.=)
n.1434C>T
10g.121517405G>CCA378328191FGFR2c.998C>G (p.Thr333Ser)
c.731C>G (p.Thr244Ser)
c.1004C>G (p.Thr335Ser)
c.653C>G (p.Thr218Ser)
c.820+1277C>G (p.=)
c.1087+1277C>G (p.=)
c.742+1277C>G (p.=)
c.939+2574C>G (p.=)
c.749-2086C>G (p.=)
n.207C>G
c.314C>G (p.Thr105Ser)
n.1407C>G
c.*45C>G (p.=)
n.1448C>G
c.1144+1277C>G (p.=)
c.1055C>G (p.Thr352Ser)
c.877+1277C>G (p.=)
c.799+1277C>G (p.=)
c.710C>G (p.Thr237Ser)
c.788C>G (p.Thr263Ser)
c.-173C>G (p.=)
n.1434C>G
10g.121517405G>TCA378328194FGFR2c.998C>A (p.Thr333Asn)
c.731C>A (p.Thr244Asn)
c.1004C>A (p.Thr335Asn)
c.653C>A (p.Thr218Asn)
c.820+1277C>A (p.=)
c.1087+1277C>A (p.=)
c.742+1277C>A (p.=)
c.939+2574C>A (p.=)
c.749-2086C>A (p.=)
n.207C>A
c.314C>A (p.Thr105Asn)
n.1407C>A
c.*45C>A (p.=)
n.1448C>A
c.1144+1277C>A (p.=)
c.1055C>A (p.Thr352Asn)
c.877+1277C>A (p.=)
c.799+1277C>A (p.=)
c.710C>A (p.Thr237Asn)
c.788C>A (p.Thr263Asn)
c.-173C>A (p.=)
n.1434C>A
10g.121517406T>ACA378328200FGFR2c.997A>T (p.Thr333Ser)
c.730A>T (p.Thr244Ser)
c.1003A>T (p.Thr335Ser)
c.652A>T (p.Thr218Ser)
c.820+1276A>T (p.=)
c.1087+1276A>T (p.=)
c.742+1276A>T (p.=)
c.939+2573A>T (p.=)
c.749-2087A>T (p.=)
n.206A>T
c.313A>T (p.Thr105Ser)
n.1406A>T
c.*44A>T (p.=)
n.1447A>T
c.1144+1276A>T (p.=)
c.1054A>T (p.Thr352Ser)
c.877+1276A>T (p.=)
c.799+1276A>T (p.=)
c.709A>T (p.Thr237Ser)
c.787A>T (p.Thr263Ser)
c.-174A>T (p.=)
n.1433A>T

Number of alleles fetched