Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121517383A>CCA378328014FGFR2c.1020T>G (p.Tyr340Ter)
c.753T>G (p.Tyr251Ter)
c.1026T>G (p.Tyr342Ter)
c.675T>G (p.Tyr225Ter)
c.820+1299T>G (p.=)
c.1087+1299T>G (p.=)
c.742+1299T>G (p.=)
c.939+2596T>G (p.=)
c.749-2064T>G (p.=)
n.229T>G
c.336T>G (p.Tyr112Ter)
n.1429T>G
c.*67T>G (p.=)
n.1470T>G
c.1144+1299T>G (p.=)
c.1077T>G (p.Tyr359Ter)
c.877+1299T>G (p.=)
c.799+1299T>G (p.=)
c.732T>G (p.Tyr244Ter)
c.810T>G (p.Tyr270Ter)
c.-151T>G (p.=)
n.1456T>G
10g.121517383A>TCA378328017FGFR2c.1020T>A (p.Tyr340Ter)
c.753T>A (p.Tyr251Ter)
c.1026T>A (p.Tyr342Ter)
c.675T>A (p.Tyr225Ter)
c.820+1299T>A (p.=)
c.1087+1299T>A (p.=)
c.742+1299T>A (p.=)
c.939+2596T>A (p.=)
c.749-2064T>A (p.=)
n.229T>A
c.336T>A (p.Tyr112Ter)
n.1429T>A
c.*67T>A (p.=)
n.1470T>A
c.1144+1299T>A (p.=)
c.1077T>A (p.Tyr359Ter)
c.877+1299T>A (p.=)
c.799+1299T>A (p.=)
c.732T>A (p.Tyr244Ter)
c.810T>A (p.Tyr270Ter)
c.-151T>A (p.=)
n.1456T>A
10g.121517384T>ACA378328021FGFR2c.1019A>T (p.Tyr340Phe)
c.752A>T (p.Tyr251Phe)
c.1025A>T (p.Tyr342Phe)
c.674A>T (p.Tyr225Phe)
c.820+1298A>T (p.=)
c.1087+1298A>T (p.=)
c.742+1298A>T (p.=)
c.939+2595A>T (p.=)
c.749-2065A>T (p.=)
n.228A>T
c.335A>T (p.Tyr112Phe)
n.1428A>T
c.*66A>T (p.=)
n.1469A>T
c.1144+1298A>T (p.=)
c.1076A>T (p.Tyr359Phe)
c.877+1298A>T (p.=)
c.799+1298A>T (p.=)
c.731A>T (p.Tyr244Phe)
c.809A>T (p.Tyr270Phe)
c.-152A>T (p.=)
n.1455A>T
10g.121517384T>CCA378328024FGFR2c.1019A>G (p.Tyr340Cys)
c.752A>G (p.Tyr251Cys)
c.1025A>G (p.Tyr342Cys)
c.674A>G (p.Tyr225Cys)
c.820+1298A>G (p.=)
c.1087+1298A>G (p.=)
c.742+1298A>G (p.=)
c.939+2595A>G (p.=)
c.749-2065A>G (p.=)
n.228A>G
c.335A>G (p.Tyr112Cys)
n.1428A>G
c.*66A>G (p.=)
n.1469A>G
c.1144+1298A>G (p.=)
c.1076A>G (p.Tyr359Cys)
c.877+1298A>G (p.=)
c.799+1298A>G (p.=)
c.731A>G (p.Tyr244Cys)
c.809A>G (p.Tyr270Cys)
c.-152A>G (p.=)
n.1455A>G
ClinVar
10g.121517384T>GCA378328027FGFR2c.1019A>C (p.Tyr340Ser)
c.752A>C (p.Tyr251Ser)
c.1025A>C (p.Tyr342Ser)
c.674A>C (p.Tyr225Ser)
c.820+1298A>C (p.=)
c.1087+1298A>C (p.=)
c.742+1298A>C (p.=)
c.939+2595A>C (p.=)
c.749-2065A>C (p.=)
n.228A>C
c.335A>C (p.Tyr112Ser)
n.1428A>C
c.*66A>C (p.=)
n.1469A>C
c.1144+1298A>C (p.=)
c.1076A>C (p.Tyr359Ser)
c.877+1298A>C (p.=)
c.799+1298A>C (p.=)
c.731A>C (p.Tyr244Ser)
c.809A>C (p.Tyr270Ser)
c.-152A>C (p.=)
n.1455A>C
10g.121517384T=CA1941024605FGFR2c.1019A= (p.Tyr340=)
c.752A= (p.Tyr251=)
c.1025A= (p.Tyr342=)
c.674A= (p.Tyr225=)
c.820+1298A= (p.=)
c.1087+1298A= (p.=)
c.742+1298A= (p.=)
c.939+2595A= (p.=)
c.749-2065A= (p.=)
n.228A=
c.335A= (p.Tyr112=)
n.1428A=
c.*66A= (p.=)
n.1469A=
c.1144+1298A= (p.=)
c.1076A= (p.Tyr359=)
c.877+1298A= (p.=)
c.799+1298A= (p.=)
c.731A= (p.Tyr244=)
c.809A= (p.Tyr270=)
c.-152A= (p.=)
n.1455A=
10g.121517385A=CA1941024606FGFR2c.1018T= (p.Tyr340=)
c.751T= (p.Tyr251=)
c.1024T= (p.Tyr342=)
c.673T= (p.Tyr225=)
c.820+1297T= (p.=)
c.1087+1297T= (p.=)
c.742+1297T= (p.=)
c.939+2594T= (p.=)
c.749-2066T= (p.=)
n.227T=
c.334T= (p.Tyr112=)
n.1427T=
c.*65T= (p.=)
n.1468T=
c.1144+1297T= (p.=)
c.1075T= (p.Tyr359=)
c.877+1297T= (p.=)
c.799+1297T= (p.=)
c.730T= (p.Tyr244=)
c.808T= (p.Tyr270=)
c.-153T= (p.=)
n.1454T=
10g.121517385A>CCA378328030FGFR2c.1018T>G (p.Tyr340Asp)
c.751T>G (p.Tyr251Asp)
c.1024T>G (p.Tyr342Asp)
c.673T>G (p.Tyr225Asp)
c.820+1297T>G (p.=)
c.1087+1297T>G (p.=)
c.742+1297T>G (p.=)
c.939+2594T>G (p.=)
c.749-2066T>G (p.=)
n.227T>G
c.334T>G (p.Tyr112Asp)
n.1427T>G
c.*65T>G (p.=)
n.1468T>G
c.1144+1297T>G (p.=)
c.1075T>G (p.Tyr359Asp)
c.877+1297T>G (p.=)
c.799+1297T>G (p.=)
c.730T>G (p.Tyr244Asp)
c.808T>G (p.Tyr270Asp)
c.-153T>G (p.=)
n.1454T>G
10g.121517385A>GCA280169FGFR2c.1018T>C (p.Tyr340His)
c.751T>C (p.Tyr251His)
c.1024T>C (p.Tyr342His)
c.673T>C (p.Tyr225His)
c.820+1297T>C (p.=)
c.1087+1297T>C (p.=)
c.742+1297T>C (p.=)
c.939+2594T>C (p.=)
c.749-2066T>C (p.=)
n.227T>C
c.334T>C (p.Tyr112His)
n.1427T>C
c.*65T>C (p.=)
n.1468T>C
c.1144+1297T>C (p.=)
c.1075T>C (p.Tyr359His)
c.877+1297T>C (p.=)
c.799+1297T>C (p.=)
c.730T>C (p.Tyr244His)
c.808T>C (p.Tyr270His)
c.-153T>C (p.=)
n.1454T>C
ClinVar dbSNP
10g.121517385A>TCA378328034FGFR2c.1018T>A (p.Tyr340Asn)
c.751T>A (p.Tyr251Asn)
c.1024T>A (p.Tyr342Asn)
c.673T>A (p.Tyr225Asn)
c.820+1297T>A (p.=)
c.1087+1297T>A (p.=)
c.742+1297T>A (p.=)
c.939+2594T>A (p.=)
c.749-2066T>A (p.=)
n.227T>A
c.334T>A (p.Tyr112Asn)
n.1427T>A
c.*65T>A (p.=)
n.1468T>A
c.1144+1297T>A (p.=)
c.1075T>A (p.Tyr359Asn)
c.877+1297T>A (p.=)
c.799+1297T>A (p.=)
c.730T>A (p.Tyr244Asn)
c.808T>A (p.Tyr270Asn)
c.-153T>A (p.=)
n.1454T>A
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.121517386T>ACA378328039FGFR2c.1017A>T (p.Glu339Asp)
c.750A>T (p.Glu250Asp)
c.1023A>T (p.Glu341Asp)
c.672A>T (p.Glu224Asp)
c.820+1296A>T (p.=)
c.1087+1296A>T (p.=)
c.742+1296A>T (p.=)
c.939+2593A>T (p.=)
c.749-2067A>T (p.=)
n.226A>T
c.333A>T (p.Glu111Asp)
n.1426A>T
c.*64A>T (p.=)
n.1467A>T
c.1144+1296A>T (p.=)
c.1074A>T (p.Glu358Asp)
c.877+1296A>T (p.=)
c.799+1296A>T (p.=)
c.729A>T (p.Glu243Asp)
c.807A>T (p.Glu269Asp)
c.-154A>T (p.=)
n.1453A>T
10g.121517386T>CCA596347241FGFR2c.1017A>G (p.Glu339=)
c.750A>G (p.Glu250=)
c.1023A>G (p.Glu341=)
c.672A>G (p.Glu224=)
c.820+1296A>G (p.=)
c.1087+1296A>G (p.=)
c.742+1296A>G (p.=)
c.939+2593A>G (p.=)
c.749-2067A>G (p.=)
n.226A>G
c.333A>G (p.Glu111=)
n.1426A>G
c.*64A>G (p.=)
n.1467A>G
c.1144+1296A>G (p.=)
c.1074A>G (p.Glu358=)
c.877+1296A>G (p.=)
c.799+1296A>G (p.=)
c.729A>G (p.Glu243=)
c.807A>G (p.Glu269=)
c.-154A>G (p.=)
n.1453A>G
gnomAD
10g.121517386T>GCA378328042FGFR2c.1017A>C (p.Glu339Asp)
c.750A>C (p.Glu250Asp)
c.1023A>C (p.Glu341Asp)
c.672A>C (p.Glu224Asp)
c.820+1296A>C (p.=)
c.1087+1296A>C (p.=)
c.742+1296A>C (p.=)
c.939+2593A>C (p.=)
c.749-2067A>C (p.=)
n.226A>C
c.333A>C (p.Glu111Asp)
n.1426A>C
c.*64A>C (p.=)
n.1467A>C
c.1144+1296A>C (p.=)
c.1074A>C (p.Glu358Asp)
c.877+1296A>C (p.=)
c.799+1296A>C (p.=)
c.729A>C (p.Glu243Asp)
c.807A>C (p.Glu269Asp)
c.-154A>C (p.=)
n.1453A>C
10g.121517386T=CA1941024607FGFR2c.1017A= (p.Glu339=)
c.750A= (p.Glu250=)
c.1023A= (p.Glu341=)
c.672A= (p.Glu224=)
c.820+1296A= (p.=)
c.1087+1296A= (p.=)
c.742+1296A= (p.=)
c.939+2593A= (p.=)
c.749-2067A= (p.=)
n.226A=
c.333A= (p.Glu111=)
n.1426A=
c.*64A= (p.=)
n.1467A=
c.1144+1296A= (p.=)
c.1074A= (p.Glu358=)
c.877+1296A= (p.=)
c.799+1296A= (p.=)
c.729A= (p.Glu243=)
c.807A= (p.Glu269=)
c.-154A= (p.=)
n.1453A=
10g.121517387T>ACA378328050FGFR2c.1016A>T (p.Glu339Val)
c.749A>T (p.Glu250Val)
c.1022A>T (p.Glu341Val)
c.671A>T (p.Glu224Val)
c.820+1295A>T (p.=)
c.1087+1295A>T (p.=)
c.742+1295A>T (p.=)
c.939+2592A>T (p.=)
c.749-2068A>T (p.=)
n.225A>T
c.332A>T (p.Glu111Val)
n.1425A>T
c.*63A>T (p.=)
n.1466A>T
c.1144+1295A>T (p.=)
c.1073A>T (p.Glu358Val)
c.877+1295A>T (p.=)
c.799+1295A>T (p.=)
c.728A>T (p.Glu243Val)
c.806A>T (p.Glu269Val)
c.-155A>T (p.=)
n.1452A>T
10g.121517387T>CCA378328053FGFR2c.1016A>G (p.Glu339Gly)
c.749A>G (p.Glu250Gly)
c.1022A>G (p.Glu341Gly)
c.671A>G (p.Glu224Gly)
c.820+1295A>G (p.=)
c.1087+1295A>G (p.=)
c.742+1295A>G (p.=)
c.939+2592A>G (p.=)
c.749-2068A>G (p.=)
n.225A>G
c.332A>G (p.Glu111Gly)
n.1425A>G
c.*63A>G (p.=)
n.1466A>G
c.1144+1295A>G (p.=)
c.1073A>G (p.Glu358Gly)
c.877+1295A>G (p.=)
c.799+1295A>G (p.=)
c.728A>G (p.Glu243Gly)
c.806A>G (p.Glu269Gly)
c.-155A>G (p.=)
n.1452A>G
10g.121517387T>GCA378328046FGFR2c.1016A>C (p.Glu339Ala)
c.749A>C (p.Glu250Ala)
c.1022A>C (p.Glu341Ala)
c.671A>C (p.Glu224Ala)
c.820+1295A>C (p.=)
c.1087+1295A>C (p.=)
c.742+1295A>C (p.=)
c.939+2592A>C (p.=)
c.749-2068A>C (p.=)
n.225A>C
c.332A>C (p.Glu111Ala)
n.1425A>C
c.*63A>C (p.=)
n.1466A>C
c.1144+1295A>C (p.=)
c.1073A>C (p.Glu358Ala)
c.877+1295A>C (p.=)
c.799+1295A>C (p.=)
c.728A>C (p.Glu243Ala)
c.806A>C (p.Glu269Ala)
c.-155A>C (p.=)
n.1452A>C
10g.121517388C>ACA378328055FGFR2c.1015G>T (p.Glu339Ter)
c.748G>T (p.Glu250Ter)
c.1021G>T (p.Glu341Ter)
c.670G>T (p.Glu224Ter)
c.820+1294G>T (p.=)
c.1087+1294G>T (p.=)
c.742+1294G>T (p.=)
c.939+2591G>T (p.=)
c.749-2069G>T (p.=)
n.224G>T
c.331G>T (p.Glu111Ter)
n.1424G>T
c.*62G>T (p.=)
n.1465G>T
c.1144+1294G>T (p.=)
c.1072G>T (p.Glu358Ter)
c.877+1294G>T (p.=)
c.799+1294G>T (p.=)
c.727G>T (p.Glu243Ter)
c.805G>T (p.Glu269Ter)
c.-156G>T (p.=)
n.1451G>T
10g.121517388C=CA1941024608FGFR2c.1015G= (p.Glu339=)
c.748G= (p.Glu250=)
c.1021G= (p.Glu341=)
c.670G= (p.Glu224=)
c.820+1294G= (p.=)
c.1087+1294G= (p.=)
c.742+1294G= (p.=)
c.939+2591G= (p.=)
c.749-2069G= (p.=)
n.224G=
c.331G= (p.Glu111=)
n.1424G=
c.*62G= (p.=)
n.1465G=
c.1144+1294G= (p.=)
c.1072G= (p.Glu358=)
c.877+1294G= (p.=)
c.799+1294G= (p.=)
c.727G= (p.Glu243=)
c.805G= (p.Glu269=)
c.-156G= (p.=)
n.1451G=
10g.121517388C>GCA378328058FGFR2c.1015G>C (p.Glu339Gln)
c.748G>C (p.Glu250Gln)
c.1021G>C (p.Glu341Gln)
c.670G>C (p.Glu224Gln)
c.820+1294G>C (p.=)
c.1087+1294G>C (p.=)
c.742+1294G>C (p.=)
c.939+2591G>C (p.=)
c.749-2069G>C (p.=)
n.224G>C
c.331G>C (p.Glu111Gln)
n.1424G>C
c.*62G>C (p.=)
n.1465G>C
c.1144+1294G>C (p.=)
c.1072G>C (p.Glu358Gln)
c.877+1294G>C (p.=)
c.799+1294G>C (p.=)
c.727G>C (p.Glu243Gln)
c.805G>C (p.Glu269Gln)
c.-156G>C (p.=)
n.1451G>C
10g.121517388C>TCA378328061FGFR2c.1015G>A (p.Glu339Lys)
c.748G>A (p.Glu250Lys)
c.1021G>A (p.Glu341Lys)
c.670G>A (p.Glu224Lys)
c.820+1294G>A (p.=)
c.1087+1294G>A (p.=)
c.742+1294G>A (p.=)
c.939+2591G>A (p.=)
c.749-2069G>A (p.=)
n.224G>A
c.331G>A (p.Glu111Lys)
n.1424G>A
c.*62G>A (p.=)
n.1465G>A
c.1144+1294G>A (p.=)
c.1072G>A (p.Glu358Lys)
c.877+1294G>A (p.=)
c.799+1294G>A (p.=)
c.727G>A (p.Glu243Lys)
c.805G>A (p.Glu269Lys)
c.-156G>A (p.=)
n.1451G>A
10g.121517389C=CA1941024609FGFR2c.1014G= (p.Gly338=)
c.747G= (p.Gly249=)
c.1020G= (p.Gly340=)
c.669G= (p.Gly223=)
c.820+1293G= (p.=)
c.1087+1293G= (p.=)
c.742+1293G= (p.=)
c.939+2590G= (p.=)
c.749-2070G= (p.=)
n.223G=
c.330G= (p.Gly110=)
n.1423G=
c.*61G= (p.=)
n.1464G=
c.1144+1293G= (p.=)
c.1071G= (p.Gly357=)
c.877+1293G= (p.=)
c.799+1293G= (p.=)
c.726G= (p.Gly242=)
c.804G= (p.Gly268=)
c.-157G= (p.=)
n.1450G=
10g.121517389C>TCA214310200FGFR2c.1014G>A (p.Gly338=)
c.747G>A (p.Gly249=)
c.1020G>A (p.Gly340=)
c.669G>A (p.Gly223=)
c.820+1293G>A (p.=)
c.1087+1293G>A (p.=)
c.742+1293G>A (p.=)
c.939+2590G>A (p.=)
c.749-2070G>A (p.=)
n.223G>A
c.330G>A (p.Gly110=)
n.1423G>A
c.*61G>A (p.=)
n.1464G>A
c.1144+1293G>A (p.=)
c.1071G>A (p.Gly357=)
c.877+1293G>A (p.=)
c.799+1293G>A (p.=)
c.726G>A (p.Gly242=)
c.804G>A (p.Gly268=)
c.-157G>A (p.=)
n.1450G>A
dbSNP gnomAD COSMIC COSMIC COSMIC
10g.121517390C>ACA378328078FGFR2c.1013G>T (p.Gly338Val)
c.746G>T (p.Gly249Val)
c.1019G>T (p.Gly340Val)
c.668G>T (p.Gly223Val)
c.820+1292G>T (p.=)
c.1087+1292G>T (p.=)
c.742+1292G>T (p.=)
c.939+2589G>T (p.=)
c.749-2071G>T (p.=)
n.222G>T
c.329G>T (p.Gly110Val)
n.1422G>T
c.*60G>T (p.=)
n.1463G>T
c.1144+1292G>T (p.=)
c.1070G>T (p.Gly357Val)
c.877+1292G>T (p.=)
c.799+1292G>T (p.=)
c.725G>T (p.Gly242Val)
c.803G>T (p.Gly268Val)
c.-158G>T (p.=)
n.1449G>T
10g.121517390C=CA1941024610FGFR2c.1013G= (p.Gly338=)
c.746G= (p.Gly249=)
c.1019G= (p.Gly340=)
c.668G= (p.Gly223=)
c.820+1292G= (p.=)
c.1087+1292G= (p.=)
c.742+1292G= (p.=)
c.939+2589G= (p.=)
c.749-2071G= (p.=)
n.222G=
c.329G= (p.Gly110=)
n.1422G=
c.*60G= (p.=)
n.1463G=
c.1144+1292G= (p.=)
c.1070G= (p.Gly357=)
c.877+1292G= (p.=)
c.799+1292G= (p.=)
c.725G= (p.Gly242=)
c.803G= (p.Gly268=)
c.-158G= (p.=)
n.1449G=
10g.121517390C>GCA378328082FGFR2c.1013G>C (p.Gly338Ala)
c.746G>C (p.Gly249Ala)
c.1019G>C (p.Gly340Ala)
c.668G>C (p.Gly223Ala)
c.820+1292G>C (p.=)
c.1087+1292G>C (p.=)
c.742+1292G>C (p.=)
c.939+2589G>C (p.=)
c.749-2071G>C (p.=)
n.222G>C
c.329G>C (p.Gly110Ala)
n.1422G>C
c.*60G>C (p.=)
n.1463G>C
c.1144+1292G>C (p.=)
c.1070G>C (p.Gly357Ala)
c.877+1292G>C (p.=)
c.799+1292G>C (p.=)
c.725G>C (p.Gly242Ala)
c.803G>C (p.Gly268Ala)
c.-158G>C (p.=)
n.1449G>C
10g.121517390C>TCA16043911FGFR2c.1013G>A (p.Gly338Glu)
c.746G>A (p.Gly249Glu)
c.1019G>A (p.Gly340Glu)
c.668G>A (p.Gly223Glu)
c.820+1292G>A (p.=)
c.1087+1292G>A (p.=)
c.742+1292G>A (p.=)
c.939+2589G>A (p.=)
c.749-2071G>A (p.=)
n.222G>A
c.329G>A (p.Gly110Glu)
n.1422G>A
c.*60G>A (p.=)
n.1463G>A
c.1144+1292G>A (p.=)
c.1070G>A (p.Gly357Glu)
c.877+1292G>A (p.=)
c.799+1292G>A (p.=)
c.725G>A (p.Gly242Glu)
c.803G>A (p.Gly268Glu)
c.-158G>A (p.=)
n.1449G>A
ClinVar
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

Number of alleles fetched