Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121574384A>CCA933278320FGFR2c.110-8680T>G (p.=)
c.110-9805T>G (p.=)
c.109+19325T>G (p.=)
n.371-8680T>G
n.57-8680T>G
n.756+19325T>G
c.167-8680T>G (p.=)
c.167-9805T>G (p.=)
c.166+19325T>G (p.=)
n.742+19325T>G
10g.121574387G>CCA1941050945FGFR2c.110-8683C>G (p.=)
c.110-9808C>G (p.=)
c.109+19322C>G (p.=)
n.371-8683C>G
n.57-8683C>G
n.756+19322C>G
c.167-8683C>G (p.=)
c.167-9808C>G (p.=)
c.166+19322C>G (p.=)
n.742+19322C>G
10g.121574387G=CA1941050944FGFR2c.110-8683C= (p.=)
c.110-9808C= (p.=)
c.109+19322C= (p.=)
n.371-8683C=
n.57-8683C=
n.756+19322C=
c.167-8683C= (p.=)
c.167-9808C= (p.=)
c.166+19322C= (p.=)
n.742+19322C=
10g.121574390A=CA1941050946FGFR2c.110-8686T= (p.=)
c.110-9811T= (p.=)
c.109+19319T= (p.=)
n.371-8686T=
n.57-8686T=
n.756+19319T=
c.167-8686T= (p.=)
c.167-9811T= (p.=)
c.166+19319T= (p.=)
n.742+19319T=
10g.121574390A>GCA933278322FGFR2c.110-8686T>C (p.=)
c.110-9811T>C (p.=)
c.109+19319T>C (p.=)
n.371-8686T>C
n.57-8686T>C
n.756+19319T>C
c.167-8686T>C (p.=)
c.167-9811T>C (p.=)
c.166+19319T>C (p.=)
n.742+19319T>C
10g.121574391T>CCA1941050948FGFR2c.110-8687A>G (p.=)
c.110-9812A>G (p.=)
c.109+19318A>G (p.=)
n.371-8687A>G
n.57-8687A>G
n.756+19318A>G
c.167-8687A>G (p.=)
c.167-9812A>G (p.=)
c.166+19318A>G (p.=)
n.742+19318A>G
10g.121574391T=CA1941050947FGFR2c.110-8687A= (p.=)
c.110-9812A= (p.=)
c.109+19318A= (p.=)
n.371-8687A=
n.57-8687A=
n.756+19318A=
c.167-8687A= (p.=)
c.167-9812A= (p.=)
c.166+19318A= (p.=)
n.742+19318A=
10g.121574392G>ACA660815378FGFR2c.110-8688C>T (p.=)
c.110-9813C>T (p.=)
c.109+19317C>T (p.=)
n.371-8688C>T
n.57-8688C>T
n.756+19317C>T
c.167-8688C>T (p.=)
c.167-9813C>T (p.=)
c.166+19317C>T (p.=)
n.742+19317C>T
10g.121574392G=CA1941050949FGFR2c.110-8688C= (p.=)
c.110-9813C= (p.=)
c.109+19317C= (p.=)
n.371-8688C=
n.57-8688C=
n.756+19317C=
c.167-8688C= (p.=)
c.167-9813C= (p.=)
c.166+19317C= (p.=)
n.742+19317C=
10g.121574393G>ACA1941050951FGFR2c.110-8689C>T (p.=)
c.110-9814C>T (p.=)
c.109+19316C>T (p.=)
n.371-8689C>T
n.57-8689C>T
n.756+19316C>T
c.167-8689C>T (p.=)
c.167-9814C>T (p.=)
c.166+19316C>T (p.=)
n.742+19316C>T
10g.121574393G=CA1941050950FGFR2c.110-8689C= (p.=)
c.110-9814C= (p.=)
c.109+19316C= (p.=)
n.371-8689C=
n.57-8689C=
n.756+19316C=
c.167-8689C= (p.=)
c.167-9814C= (p.=)
c.166+19316C= (p.=)
n.742+19316C=
10g.121574396G>CCA660815381FGFR2c.110-8692C>G (p.=)
c.110-9817C>G (p.=)
c.109+19313C>G (p.=)
n.371-8692C>G
n.57-8692C>G
n.756+19313C>G
c.167-8692C>G (p.=)
c.167-9817C>G (p.=)
c.166+19313C>G (p.=)
n.742+19313C>G
10g.121574396G=CA1941050952FGFR2c.110-8692C= (p.=)
c.110-9817C= (p.=)
c.109+19313C= (p.=)
n.371-8692C=
n.57-8692C=
n.756+19313C=
c.167-8692C= (p.=)
c.167-9817C= (p.=)
c.166+19313C= (p.=)
n.742+19313C=
10g.121574396G>TCA1941050953FGFR2c.110-8692C>A (p.=)
c.110-9817C>A (p.=)
c.109+19313C>A (p.=)
n.371-8692C>A
n.57-8692C>A
n.756+19313C>A
c.167-8692C>A (p.=)
c.167-9817C>A (p.=)
c.166+19313C>A (p.=)
n.742+19313C>A
10g.121574400G>ACA596349062FGFR2c.110-8696C>T (p.=)
c.110-9821C>T (p.=)
c.109+19309C>T (p.=)
n.371-8696C>T
n.57-8696C>T
n.756+19309C>T
c.167-8696C>T (p.=)
c.167-9821C>T (p.=)
c.166+19309C>T (p.=)
n.742+19309C>T
gnomAD
10g.121574400G=CA1941050954FGFR2c.110-8696C= (p.=)
c.110-9821C= (p.=)
c.109+19309C= (p.=)
n.371-8696C=
n.57-8696C=
n.756+19309C=
c.167-8696C= (p.=)
c.167-9821C= (p.=)
c.166+19309C= (p.=)
n.742+19309C=
10g.121574403C>ACA596349064FGFR2c.110-8699G>T (p.=)
c.110-9824G>T (p.=)
c.109+19306G>T (p.=)
n.371-8699G>T
n.57-8699G>T
n.756+19306G>T
c.167-8699G>T (p.=)
c.167-9824G>T (p.=)
c.166+19306G>T (p.=)
n.742+19306G>T
gnomAD
10g.121574403C=CA1941050955FGFR2c.110-8699G= (p.=)
c.110-9824G= (p.=)
c.109+19306G= (p.=)
n.371-8699G=
n.57-8699G=
n.756+19306G=
c.167-8699G= (p.=)
c.167-9824G= (p.=)
c.166+19306G= (p.=)
n.742+19306G=
10g.121574406G>ACA1941050957FGFR2c.110-8702C>T (p.=)
c.110-9827C>T (p.=)
c.109+19303C>T (p.=)
n.371-8702C>T
n.57-8702C>T
n.756+19303C>T
c.167-8702C>T (p.=)
c.167-9827C>T (p.=)
c.166+19303C>T (p.=)
n.742+19303C>T
10g.121574406G=CA1941050956FGFR2c.110-8702C= (p.=)
c.110-9827C= (p.=)
c.109+19303C= (p.=)
n.371-8702C=
n.57-8702C=
n.756+19303C=
c.167-8702C= (p.=)
c.167-9827C= (p.=)
c.166+19303C= (p.=)
n.742+19303C=
10g.121574407T>CCA653784059FGFR2c.110-8703A>G (p.=)
c.110-9828A>G (p.=)
c.109+19302A>G (p.=)
n.371-8703A>G
n.57-8703A>G
n.756+19302A>G
c.167-8703A>G (p.=)
c.167-9828A>G (p.=)
c.166+19302A>G (p.=)
n.742+19302A>G
COSMIC COSMIC
10g.121574407T=CA1941050958FGFR2c.110-8703A= (p.=)
c.110-9828A= (p.=)
c.109+19302A= (p.=)
n.371-8703A=
n.57-8703A=
n.756+19302A=
c.167-8703A= (p.=)
c.167-9828A= (p.=)
c.166+19302A= (p.=)
n.742+19302A=
10g.121574409G=CA1941050959FGFR2c.110-8705C= (p.=)
c.110-9830C= (p.=)
c.109+19300C= (p.=)
n.371-8705C=
n.57-8705C=
n.756+19300C=
c.167-8705C= (p.=)
c.167-9830C= (p.=)
c.166+19300C= (p.=)
n.742+19300C=
10g.121574409G>TCA596349067FGFR2c.110-8705C>A (p.=)
c.110-9830C>A (p.=)
c.109+19300C>A (p.=)
n.371-8705C>A
n.57-8705C>A
n.756+19300C>A
c.167-8705C>A (p.=)
c.167-9830C>A (p.=)
c.166+19300C>A (p.=)
n.742+19300C>A
gnomAD
10g.121574411C=CA1941050961FGFR2c.110-8707G= (p.=)
c.110-9832G= (p.=)
c.109+19298G= (p.=)
n.371-8707G=
n.57-8707G=
n.756+19298G=
c.167-8707G= (p.=)
c.167-9832G= (p.=)
c.166+19298G= (p.=)
n.742+19298G=
10g.121574411C>TCA1941050960FGFR2c.110-8707G>A (p.=)
c.110-9832G>A (p.=)
c.109+19298G>A (p.=)
n.371-8707G>A
n.57-8707G>A
n.756+19298G>A
c.167-8707G>A (p.=)
c.167-9832G>A (p.=)
c.166+19298G>A (p.=)
n.742+19298G>A
10g.121574414A=CA1941050962FGFR2c.110-8710T= (p.=)
c.110-9835T= (p.=)
c.109+19295T= (p.=)
n.371-8710T=
n.57-8710T=
n.756+19295T=
c.167-8710T= (p.=)
c.167-9835T= (p.=)
c.166+19295T= (p.=)
n.742+19295T=
10g.121574414A>GCA214307343FGFR2c.110-8710T>C (p.=)
c.110-9835T>C (p.=)
c.109+19295T>C (p.=)
n.371-8710T>C
n.57-8710T>C
n.756+19295T>C
c.167-8710T>C (p.=)
c.167-9835T>C (p.=)
c.166+19295T>C (p.=)
n.742+19295T>C
dbSNP
10g.121574416C>ACA660815388FGFR2c.110-8712G>T (p.=)
c.110-9837G>T (p.=)
c.109+19293G>T (p.=)
n.371-8712G>T
n.57-8712G>T
n.756+19293G>T
c.167-8712G>T (p.=)
c.167-9837G>T (p.=)
c.166+19293G>T (p.=)
n.742+19293G>T
10g.121574416C=CA1941050963FGFR2c.110-8712G= (p.=)
c.110-9837G= (p.=)
c.109+19293G= (p.=)
n.371-8712G=
n.57-8712G=
n.756+19293G=
c.167-8712G= (p.=)
c.167-9837G= (p.=)
c.166+19293G= (p.=)
n.742+19293G=
10g.121574417T>CCA214307349FGFR2c.110-8713A>G (p.=)
c.110-9838A>G (p.=)
c.109+19292A>G (p.=)
n.371-8713A>G
n.57-8713A>G
n.756+19292A>G
c.167-8713A>G (p.=)
c.167-9838A>G (p.=)
c.166+19292A>G (p.=)
n.742+19292A>G
dbSNP
10g.121574417T=CA1941050964FGFR2c.110-8713A= (p.=)
c.110-9838A= (p.=)
c.109+19292A= (p.=)
n.371-8713A=
n.57-8713A=
n.756+19292A=
c.167-8713A= (p.=)
c.167-9838A= (p.=)
c.166+19292A= (p.=)
n.742+19292A=
10g.121574420A=CA1941050965FGFR2c.110-8716T= (p.=)
c.110-9841T= (p.=)
c.109+19289T= (p.=)
n.371-8716T=
n.57-8716T=
n.756+19289T=
c.167-8716T= (p.=)
c.167-9841T= (p.=)
c.166+19289T= (p.=)
n.742+19289T=
10g.121574420A>GCA660815390FGFR2c.110-8716T>C (p.=)
c.110-9841T>C (p.=)
c.109+19289T>C (p.=)
n.371-8716T>C
n.57-8716T>C
n.756+19289T>C
c.167-8716T>C (p.=)
c.167-9841T>C (p.=)
c.166+19289T>C (p.=)
n.742+19289T>C
10g.121574421C=CA1941050966FGFR2c.110-8717G= (p.=)
c.110-9842G= (p.=)
c.109+19288G= (p.=)
n.371-8717G=
n.57-8717G=
n.756+19288G=
c.167-8717G= (p.=)
c.167-9842G= (p.=)
c.166+19288G= (p.=)
n.742+19288G=
10g.121574421C>TCA214307352FGFR2c.110-8717G>A (p.=)
c.110-9842G>A (p.=)
c.109+19288G>A (p.=)
n.371-8717G>A
n.57-8717G>A
n.756+19288G>A
c.167-8717G>A (p.=)
c.167-9842G>A (p.=)
c.166+19288G>A (p.=)
n.742+19288G>A
dbSNP gnomAD
10g.121574422G>ACA933278329FGFR2c.110-8718C>T (p.=)
c.110-9843C>T (p.=)
c.109+19287C>T (p.=)
n.371-8718C>T
n.57-8718C>T
n.756+19287C>T
c.167-8718C>T (p.=)
c.167-9843C>T (p.=)
c.166+19287C>T (p.=)
n.742+19287C>T
10g.121574422G>CCA1941050968FGFR2c.110-8718C>G (p.=)
c.110-9843C>G (p.=)
c.109+19287C>G (p.=)
n.371-8718C>G
n.57-8718C>G
n.756+19287C>G
c.167-8718C>G (p.=)
c.167-9843C>G (p.=)
c.166+19287C>G (p.=)
n.742+19287C>G
10g.121574422G=CA1941050967FGFR2c.110-8718C= (p.=)
c.110-9843C= (p.=)
c.109+19287C= (p.=)
n.371-8718C=
n.57-8718C=
n.756+19287C=
c.167-8718C= (p.=)
c.167-9843C= (p.=)
c.166+19287C= (p.=)
n.742+19287C=
10g.121574426_121574427delinsAGCA1941050969FGFR2c.110-8723_110-8722delinsCT (p.=)
c.110-9848_110-9847delinsCT (p.=)
c.109+19282_109+19283delinsCT (p.=)
n.371-8723_371-8722delinsCT
n.57-8723_57-8722delinsCT
n.756+19282_756+19283delinsCT
c.167-8723_167-8722delinsCT (p.=)
c.167-9848_167-9847delinsCT (p.=)
c.166+19282_166+19283delinsCT (p.=)
n.742+19282_742+19283delinsCT
10g.121574427delCA660815393FGFR2c.110-8723del (p.=)
c.110-9848del (p.=)
c.109+19282del (p.=)
n.371-8723del
n.57-8723del
n.756+19282del
c.167-8723del (p.=)
c.167-9848del (p.=)
c.166+19282del (p.=)
n.742+19282del
dbSNP
10g.121574431A=CA1941050970FGFR2c.110-8727T= (p.=)
c.110-9852T= (p.=)
c.109+19278T= (p.=)
n.371-8727T=
n.57-8727T=
n.756+19278T=
c.167-8727T= (p.=)
c.167-9852T= (p.=)
c.166+19278T= (p.=)
n.742+19278T=
10g.121574432_121574437dupCA1941050971FGFR2c.110-8733_110-8728dup (p.=)
c.110-9858_110-9853dup (p.=)
c.109+19272_109+19277dup (p.=)
n.371-8733_371-8728dup
n.57-8733_57-8728dup
n.756+19272_756+19277dup
c.167-8733_167-8728dup (p.=)
c.167-9858_167-9853dup (p.=)
c.166+19272_166+19277dup (p.=)
n.742+19272_742+19277dup
dbSNP
10g.121574437G>ACA1941050973FGFR2c.110-8733C>T (p.=)
c.110-9858C>T (p.=)
c.109+19272C>T (p.=)
n.371-8733C>T
n.57-8733C>T
n.756+19272C>T
c.167-8733C>T (p.=)
c.167-9858C>T (p.=)
c.166+19272C>T (p.=)
n.742+19272C>T
10g.121574437G=CA1941050972FGFR2c.110-8733C= (p.=)
c.110-9858C= (p.=)
c.109+19272C= (p.=)
n.371-8733C=
n.57-8733C=
n.756+19272C=
c.167-8733C= (p.=)
c.167-9858C= (p.=)
c.166+19272C= (p.=)
n.742+19272C=
10g.121574438A=CA1941050974FGFR2c.110-8734T= (p.=)
c.110-9859T= (p.=)
c.109+19271T= (p.=)
n.371-8734T=
n.57-8734T=
n.756+19271T=
c.167-8734T= (p.=)
c.167-9859T= (p.=)
c.166+19271T= (p.=)
n.742+19271T=
10g.121574438A>GCA214307374FGFR2c.110-8734T>C (p.=)
c.110-9859T>C (p.=)
c.109+19271T>C (p.=)
n.371-8734T>C
n.57-8734T>C
n.756+19271T>C
c.167-8734T>C (p.=)
c.167-9859T>C (p.=)
c.166+19271T>C (p.=)
n.742+19271T>C
dbSNP
10g.121574439G>CCA660815400FGFR2c.110-8735C>G (p.=)
c.110-9860C>G (p.=)
c.109+19270C>G (p.=)
n.371-8735C>G
n.57-8735C>G
n.756+19270C>G
c.167-8735C>G (p.=)
c.167-9860C>G (p.=)
c.166+19270C>G (p.=)
n.742+19270C>G
10g.121574439G=CA1941050975FGFR2c.110-8735C= (p.=)
c.110-9860C= (p.=)
c.109+19270C= (p.=)
n.371-8735C=
n.57-8735C=
n.756+19270C=
c.167-8735C= (p.=)
c.167-9860C= (p.=)
c.166+19270C= (p.=)
n.742+19270C=
10g.121574440A=CA1941050976FGFR2c.110-8736T= (p.=)
c.110-9861T= (p.=)
c.109+19269T= (p.=)
n.371-8736T=
n.57-8736T=
n.756+19269T=
c.167-8736T= (p.=)
c.167-9861T= (p.=)
c.166+19269T= (p.=)
n.742+19269T=

Number of alleles fetched