Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121574483C=CA1941051003FGFR2c.110-8779G= (p.=)
c.110-9904G= (p.=)
c.109+19226G= (p.=)
n.371-8779G=
n.57-8779G=
n.756+19226G=
c.167-8779G= (p.=)
c.167-9904G= (p.=)
c.166+19226G= (p.=)
n.742+19226G=
10g.121574483C>TCA13356892FGFR2c.110-8779G>A (p.=)
c.110-9904G>A (p.=)
c.109+19226G>A (p.=)
n.371-8779G>A
n.57-8779G>A
n.756+19226G>A
c.167-8779G>A (p.=)
c.167-9904G>A (p.=)
c.166+19226G>A (p.=)
n.742+19226G>A
dbSNP gnomAD
10g.121574484G>ACA214307442FGFR2c.110-8780C>T (p.=)
c.110-9905C>T (p.=)
c.109+19225C>T (p.=)
n.371-8780C>T
n.57-8780C>T
n.756+19225C>T
c.167-8780C>T (p.=)
c.167-9905C>T (p.=)
c.166+19225C>T (p.=)
n.742+19225C>T
dbSNP gnomAD
10g.121574484G=CA1941051004FGFR2c.110-8780C= (p.=)
c.110-9905C= (p.=)
c.109+19225C= (p.=)
n.371-8780C=
n.57-8780C=
n.756+19225C=
c.167-8780C= (p.=)
c.167-9905C= (p.=)
c.166+19225C= (p.=)
n.742+19225C=
10g.121574484_121574486delinsACGCA214307438FGFR2c.110-8782_110-8780delinsCGT (p.=)
c.110-9907_110-9905delinsCGT (p.=)
c.109+19223_109+19225delinsCGT (p.=)
n.371-8782_371-8780delinsCGT
n.57-8782_57-8780delinsCGT
n.756+19223_756+19225delinsCGT
c.167-8782_167-8780delinsCGT (p.=)
c.167-9907_167-9905delinsCGT (p.=)
c.166+19223_166+19225delinsCGT (p.=)
n.742+19223_742+19225delinsCGT
dbSNP
10g.121574484_121574486delinsGCACA1941051005FGFR2c.110-8782_110-8780delinsTGC (p.=)
c.110-9907_110-9905delinsTGC (p.=)
c.109+19223_109+19225delinsTGC (p.=)
n.371-8782_371-8780delinsTGC
n.57-8782_57-8780delinsTGC
n.756+19223_756+19225delinsTGC
c.167-8782_167-8780delinsTGC (p.=)
c.167-9907_167-9905delinsTGC (p.=)
c.166+19223_166+19225delinsTGC (p.=)
n.742+19223_742+19225delinsTGC
10g.121574485C=CA1941051007FGFR2c.110-8781G= (p.=)
c.110-9906G= (p.=)
c.109+19224G= (p.=)
n.371-8781G=
n.57-8781G=
n.756+19224G=
c.167-8781G= (p.=)
c.167-9906G= (p.=)
c.166+19224G= (p.=)
n.742+19224G=
10g.121574485C>TCA1941051006FGFR2c.110-8781G>A (p.=)
c.110-9906G>A (p.=)
c.109+19224G>A (p.=)
n.371-8781G>A
n.57-8781G>A
n.756+19224G>A
c.167-8781G>A (p.=)
c.167-9906G>A (p.=)
c.166+19224G>A (p.=)
n.742+19224G>A
10g.121574486A=CA1941051008FGFR2c.110-8782T= (p.=)
c.110-9907T= (p.=)
c.109+19223T= (p.=)
n.371-8782T=
n.57-8782T=
n.756+19223T=
c.167-8782T= (p.=)
c.167-9907T= (p.=)
c.166+19223T= (p.=)
n.742+19223T=
10g.121574486A>GCA214307443FGFR2c.110-8782T>C (p.=)
c.110-9907T>C (p.=)
c.109+19223T>C (p.=)
n.371-8782T>C
n.57-8782T>C
n.756+19223T>C
c.167-8782T>C (p.=)
c.167-9907T>C (p.=)
c.166+19223T>C (p.=)
n.742+19223T>C
dbSNP gnomAD
10g.121574486A>TCA933278355FGFR2c.110-8782T>A (p.=)
c.110-9907T>A (p.=)
c.109+19223T>A (p.=)
n.371-8782T>A
n.57-8782T>A
n.756+19223T>A
c.167-8782T>A (p.=)
c.167-9907T>A (p.=)
c.166+19223T>A (p.=)
n.742+19223T>A
10g.121574487C=CA1941051009FGFR2c.110-8783G= (p.=)
c.110-9908G= (p.=)
c.109+19222G= (p.=)
n.371-8783G=
n.57-8783G=
n.756+19222G=
c.167-8783G= (p.=)
c.167-9908G= (p.=)
c.166+19222G= (p.=)
n.742+19222G=
10g.121574487C>TCA1941051010FGFR2c.110-8783G>A (p.=)
c.110-9908G>A (p.=)
c.109+19222G>A (p.=)
n.371-8783G>A
n.57-8783G>A
n.756+19222G>A
c.167-8783G>A (p.=)
c.167-9908G>A (p.=)
c.166+19222G>A (p.=)
n.742+19222G>A
10g.121574491T>CCA214307444FGFR2c.110-8787A>G (p.=)
c.110-9912A>G (p.=)
c.109+19218A>G (p.=)
n.371-8787A>G
n.57-8787A>G
n.756+19218A>G
c.167-8787A>G (p.=)
c.167-9912A>G (p.=)
c.166+19218A>G (p.=)
n.742+19218A>G
dbSNP
10g.121574491T=CA1941051011FGFR2c.110-8787A= (p.=)
c.110-9912A= (p.=)
c.109+19218A= (p.=)
n.371-8787A=
n.57-8787A=
n.756+19218A=
c.167-8787A= (p.=)
c.167-9912A= (p.=)
c.166+19218A= (p.=)
n.742+19218A=
10g.121574493C=CA1941051012FGFR2c.110-8789G= (p.=)
c.110-9914G= (p.=)
c.109+19216G= (p.=)
n.371-8789G=
n.57-8789G=
n.756+19216G=
c.167-8789G= (p.=)
c.167-9914G= (p.=)
c.166+19216G= (p.=)
n.742+19216G=
10g.121574493C>TCA1941051013FGFR2c.110-8789G>A (p.=)
c.110-9914G>A (p.=)
c.109+19216G>A (p.=)
n.371-8789G>A
n.57-8789G>A
n.756+19216G>A
c.167-8789G>A (p.=)
c.167-9914G>A (p.=)
c.166+19216G>A (p.=)
n.742+19216G>A
10g.121574495C=CA1941051014FGFR2c.110-8791G= (p.=)
c.110-9916G= (p.=)
c.109+19214G= (p.=)
n.371-8791G=
n.57-8791G=
n.756+19214G=
c.167-8791G= (p.=)
c.167-9916G= (p.=)
c.166+19214G= (p.=)
n.742+19214G=
10g.121574495C>GCA660815460FGFR2c.110-8791G>C (p.=)
c.110-9916G>C (p.=)
c.109+19214G>C (p.=)
n.371-8791G>C
n.57-8791G>C
n.756+19214G>C
c.167-8791G>C (p.=)
c.167-9916G>C (p.=)
c.166+19214G>C (p.=)
n.742+19214G>C
10g.121574506G>ACA1941051016FGFR2c.110-8802C>T (p.=)
c.110-9927C>T (p.=)
c.109+19203C>T (p.=)
n.371-8802C>T
n.57-8802C>T
n.756+19203C>T
c.167-8802C>T (p.=)
c.167-9927C>T (p.=)
c.166+19203C>T (p.=)
n.742+19203C>T
10g.121574506G=CA1941051015FGFR2c.110-8802C= (p.=)
c.110-9927C= (p.=)
c.109+19203C= (p.=)
n.371-8802C=
n.57-8802C=
n.756+19203C=
c.167-8802C= (p.=)
c.167-9927C= (p.=)
c.166+19203C= (p.=)
n.742+19203C=
10g.121574507T>CCA660815462FGFR2c.110-8803A>G (p.=)
c.110-9928A>G (p.=)
c.109+19202A>G (p.=)
n.371-8803A>G
n.57-8803A>G
n.756+19202A>G
c.167-8803A>G (p.=)
c.167-9928A>G (p.=)
c.166+19202A>G (p.=)
n.742+19202A>G
10g.121574507T=CA1941051017FGFR2c.110-8803A= (p.=)
c.110-9928A= (p.=)
c.109+19202A= (p.=)
n.371-8803A=
n.57-8803A=
n.756+19202A=
c.167-8803A= (p.=)
c.167-9928A= (p.=)
c.166+19202A= (p.=)
n.742+19202A=
10g.121574511A=CA1941051018FGFR2c.110-8807T= (p.=)
c.110-9932T= (p.=)
c.109+19198T= (p.=)
n.371-8807T=
n.57-8807T=
n.756+19198T=
c.167-8807T= (p.=)
c.167-9932T= (p.=)
c.166+19198T= (p.=)
n.742+19198T=
10g.121574511A>CCA933278358FGFR2c.110-8807T>G (p.=)
c.110-9932T>G (p.=)
c.109+19198T>G (p.=)
n.371-8807T>G
n.57-8807T>G
n.756+19198T>G
c.167-8807T>G (p.=)
c.167-9932T>G (p.=)
c.166+19198T>G (p.=)
n.742+19198T>G
10g.121574512G>ACA596349081FGFR2c.110-8808C>T (p.=)
c.110-9933C>T (p.=)
c.109+19197C>T (p.=)
n.371-8808C>T
n.57-8808C>T
n.756+19197C>T
c.167-8808C>T (p.=)
c.167-9933C>T (p.=)
c.166+19197C>T (p.=)
n.742+19197C>T
gnomAD
10g.121574512G=CA1941051019FGFR2c.110-8808C= (p.=)
c.110-9933C= (p.=)
c.109+19197C= (p.=)
n.371-8808C=
n.57-8808C=
n.756+19197C=
c.167-8808C= (p.=)
c.167-9933C= (p.=)
c.166+19197C= (p.=)
n.742+19197C=
10g.121574514A=CA1941051020FGFR2c.110-8810T= (p.=)
c.110-9935T= (p.=)
c.109+19195T= (p.=)
n.371-8810T=
n.57-8810T=
n.756+19195T=
c.167-8810T= (p.=)
c.167-9935T= (p.=)
c.166+19195T= (p.=)
n.742+19195T=
10g.121574514A>CCA214307449FGFR2c.110-8810T>G (p.=)
c.110-9935T>G (p.=)
c.109+19195T>G (p.=)
n.371-8810T>G
n.57-8810T>G
n.756+19195T>G
c.167-8810T>G (p.=)
c.167-9935T>G (p.=)
c.166+19195T>G (p.=)
n.742+19195T>G
dbSNP gnomAD
10g.121574514A>GCA1941051021FGFR2c.110-8810T>C (p.=)
c.110-9935T>C (p.=)
c.109+19195T>C (p.=)
n.371-8810T>C
n.57-8810T>C
n.756+19195T>C
c.167-8810T>C (p.=)
c.167-9935T>C (p.=)
c.166+19195T>C (p.=)
n.742+19195T>C
10g.121574515C=CA1941051022FGFR2c.110-8811G= (p.=)
c.110-9936G= (p.=)
c.109+19194G= (p.=)
n.371-8811G=
n.57-8811G=
n.756+19194G=
c.167-8811G= (p.=)
c.167-9936G= (p.=)
c.166+19194G= (p.=)
n.742+19194G=
10g.121574515C>TCA214307455FGFR2c.110-8811G>A (p.=)
c.110-9936G>A (p.=)
c.109+19194G>A (p.=)
n.371-8811G>A
n.57-8811G>A
n.756+19194G>A
c.167-8811G>A (p.=)
c.167-9936G>A (p.=)
c.166+19194G>A (p.=)
n.742+19194G>A
dbSNP
10g.121574518A>GCA933278360FGFR2c.110-8814T>C (p.=)
c.110-9939T>C (p.=)
c.109+19191T>C (p.=)
n.371-8814T>C
n.57-8814T>C
n.756+19191T>C
c.167-8814T>C (p.=)
c.167-9939T>C (p.=)
c.166+19191T>C (p.=)
n.742+19191T>C
10g.121574522C>ACA933278363FGFR2c.110-8818G>T (p.=)
c.110-9943G>T (p.=)
c.109+19187G>T (p.=)
n.371-8818G>T
n.57-8818G>T
n.756+19187G>T
c.167-8818G>T (p.=)
c.167-9943G>T (p.=)
c.166+19187G>T (p.=)
n.742+19187G>T
10g.121574522C=CA1941051023FGFR2c.110-8818G= (p.=)
c.110-9943G= (p.=)
c.109+19187G= (p.=)
n.371-8818G=
n.57-8818G=
n.756+19187G=
c.167-8818G= (p.=)
c.167-9943G= (p.=)
c.166+19187G= (p.=)
n.742+19187G=
10g.121574522C>TCA660815467FGFR2c.110-8818G>A (p.=)
c.110-9943G>A (p.=)
c.109+19187G>A (p.=)
n.371-8818G>A
n.57-8818G>A
n.756+19187G>A
c.167-8818G>A (p.=)
c.167-9943G>A (p.=)
c.166+19187G>A (p.=)
n.742+19187G>A
10g.121574527T>CCA214307459FGFR2c.110-8823A>G (p.=)
c.110-9948A>G (p.=)
c.109+19182A>G (p.=)
n.371-8823A>G
n.57-8823A>G
n.756+19182A>G
c.167-8823A>G (p.=)
c.167-9948A>G (p.=)
c.166+19182A>G (p.=)
n.742+19182A>G
dbSNP gnomAD
10g.121574527T=CA1941051024FGFR2c.110-8823A= (p.=)
c.110-9948A= (p.=)
c.109+19182A= (p.=)
n.371-8823A=
n.57-8823A=
n.756+19182A=
c.167-8823A= (p.=)
c.167-9948A= (p.=)
c.166+19182A= (p.=)
n.742+19182A=
10g.121574531A=CA1941051026FGFR2c.110-8827T= (p.=)
c.110-9952T= (p.=)
c.109+19178T= (p.=)
n.371-8827T=
n.57-8827T=
n.756+19178T=
c.167-8827T= (p.=)
c.167-9952T= (p.=)
c.166+19178T= (p.=)
n.742+19178T=
10g.121574531A>TCA214307465FGFR2c.110-8827T>A (p.=)
c.110-9952T>A (p.=)
c.109+19178T>A (p.=)
n.371-8827T>A
n.57-8827T>A
n.756+19178T>A
c.167-8827T>A (p.=)
c.167-9952T>A (p.=)
c.166+19178T>A (p.=)
n.742+19178T>A
dbSNP
10g.121574531_121574537delinsAAATAATCA1941051025FGFR2c.110-8833_110-8827delinsATTATTT (p.=)
c.110-9958_110-9952delinsATTATTT (p.=)
c.109+19172_109+19178delinsATTATTT (p.=)
n.371-8833_371-8827delinsATTATTT
n.57-8833_57-8827delinsATTATTT
n.756+19172_756+19178delinsATTATTT
c.167-8833_167-8827delinsATTATTT (p.=)
c.167-9958_167-9952delinsATTATTT (p.=)
c.166+19172_166+19178delinsATTATTT (p.=)
n.742+19172_742+19178delinsATTATTT
10g.121574533_121574534insCAACA933278383FGFR2c.110-8828_110-8827insGTT (p.=)
c.110-9953_110-9952insGTT (p.=)
c.109+19177_109+19178insGTT (p.=)
n.371-8828_371-8827insGTT
n.57-8828_57-8827insGTT
n.756+19177_756+19178insGTT
c.167-8828_167-8827insGTT (p.=)
c.167-9953_167-9952insGTT (p.=)
c.166+19177_166+19178insGTT (p.=)
n.742+19177_742+19178insGTT
dbSNP
10g.121574533_121574534insGAACA214307476FGFR2c.110-8828_110-8827insCTT (p.=)
c.110-9953_110-9952insCTT (p.=)
c.109+19177_109+19178insCTT (p.=)
n.371-8828_371-8827insCTT
n.57-8828_57-8827insCTT
n.756+19177_756+19178insCTT
c.167-8828_167-8827insCTT (p.=)
c.167-9953_167-9952insCTT (p.=)
c.166+19177_166+19178insCTT (p.=)
n.742+19177_742+19178insCTT
dbSNP dbSNP
10g.121574550_121574552dupCA214307484FGFR2c.110-8830_110-8828dup (p.=)
c.110-9955_110-9953dup (p.=)
c.109+19175_109+19177dup (p.=)
n.371-8830_371-8828dup
n.57-8830_57-8828dup
n.756+19175_756+19177dup
c.167-8830_167-8828dup (p.=)
c.167-9955_167-9953dup (p.=)
c.166+19175_166+19177dup (p.=)
n.742+19175_742+19177dup
dbSNP gnomAD
10g.121574547_121574552dupCA596349090FGFR2c.110-8833_110-8828dup (p.=)
c.110-9958_110-9953dup (p.=)
c.109+19172_109+19177dup (p.=)
n.371-8833_371-8828dup
n.57-8833_57-8828dup
n.756+19172_756+19177dup
c.167-8833_167-8828dup (p.=)
c.167-9958_167-9953dup (p.=)
c.166+19172_166+19177dup (p.=)
n.742+19172_742+19177dup
dbSNP gnomAD
10g.121574550_121574552delCA596349087FGFR2c.110-8830_110-8828del (p.=)
c.110-9955_110-9953del (p.=)
c.109+19175_109+19177del (p.=)
n.371-8830_371-8828del
n.57-8830_57-8828del
n.756+19175_756+19177del
c.167-8830_167-8828del (p.=)
c.167-9955_167-9953del (p.=)
c.166+19175_166+19177del (p.=)
n.742+19175_742+19177del
dbSNP gnomAD
10g.121574547_121574552delCA596349085FGFR2c.110-8833_110-8828del (p.=)
c.110-9958_110-9953del (p.=)
c.109+19172_109+19177del (p.=)
n.371-8833_371-8828del
n.57-8833_57-8828del
n.756+19172_756+19177del
c.167-8833_167-8828del (p.=)
c.167-9958_167-9953del (p.=)
c.166+19172_166+19177del (p.=)
n.742+19172_742+19177del
dbSNP gnomAD
10g.121574534T>ACA660815497FGFR2c.110-8830A>T (p.=)
c.110-9955A>T (p.=)
c.109+19175A>T (p.=)
n.371-8830A>T
n.57-8830A>T
n.756+19175A>T
c.167-8830A>T (p.=)
c.167-9955A>T (p.=)
c.166+19175A>T (p.=)
n.742+19175A>T
10g.121574534T=CA1941051027FGFR2c.110-8830A= (p.=)
c.110-9955A= (p.=)
c.109+19175A= (p.=)
n.371-8830A=
n.57-8830A=
n.756+19175A=
c.167-8830A= (p.=)
c.167-9955A= (p.=)
c.166+19175A= (p.=)
n.742+19175A=
10g.121574535A=CA1941051028FGFR2c.110-8831T= (p.=)
c.110-9956T= (p.=)
c.109+19174T= (p.=)
n.371-8831T=
n.57-8831T=
n.756+19174T=
c.167-8831T= (p.=)
c.167-9956T= (p.=)
c.166+19174T= (p.=)
n.742+19174T=

Number of alleles fetched