Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.185811292A>CCA11390095IGF2BP2c.239+11861T>G (p.=)
c.50+9720T>G (p.=)
c.-106+9720T>G (p.=)
c.178+13491T>G (p.=)
c.35+11861T>G (p.=)
c.-170+13491T>G (p.=)
dbSNP gnomAD
3g.185811298G>TCA89824954IGF2BP2c.239+11855C>A (p.=)
c.50+9714C>A (p.=)
c.-106+9714C>A (p.=)
c.178+13485C>A (p.=)
c.35+11855C>A (p.=)
c.-170+13485C>A (p.=)
dbSNP
3g.185811302A>GCA15257313IGF2BP2c.239+11851T>C (p.=)
c.50+9710T>C (p.=)
c.-106+9710T>C (p.=)
c.178+13481T>C (p.=)
c.35+11851T>C (p.=)
c.-170+13481T>C (p.=)
dbSNP gnomAD
3g.185811302A>TCA903846231IGF2BP2c.239+11851T>A (p.=)
c.50+9710T>A (p.=)
c.-106+9710T>A (p.=)
c.178+13481T>A (p.=)
c.35+11851T>A (p.=)
c.-170+13481T>A (p.=)
3g.185811303T>ACA548611055IGF2BP2c.239+11850A>T (p.=)
c.50+9709A>T (p.=)
c.-106+9709A>T (p.=)
c.178+13480A>T (p.=)
c.35+11850A>T (p.=)
c.-170+13480A>T (p.=)
gnomAD
3g.185811306A>CCA89824955IGF2BP2c.239+11847T>G (p.=)
c.50+9706T>G (p.=)
c.-106+9706T>G (p.=)
c.178+13477T>G (p.=)
c.35+11847T>G (p.=)
c.-170+13477T>G (p.=)
dbSNP
3g.185811306A>GCA903846232IGF2BP2c.239+11847T>C (p.=)
c.50+9706T>C (p.=)
c.-106+9706T>C (p.=)
c.178+13477T>C (p.=)
c.35+11847T>C (p.=)
c.-170+13477T>C (p.=)
3g.185811307G>TCA89824956IGF2BP2c.239+11846C>A (p.=)
c.50+9705C>A (p.=)
c.-106+9705C>A (p.=)
c.178+13476C>A (p.=)
c.35+11846C>A (p.=)
c.-170+13476C>A (p.=)
dbSNP
3g.185811311A>CCA89824957IGF2BP2c.239+11842T>G (p.=)
c.50+9701T>G (p.=)
c.-106+9701T>G (p.=)
c.178+13472T>G (p.=)
c.35+11842T>G (p.=)
c.-170+13472T>G (p.=)
dbSNP
3g.185811311A>GCA548611057IGF2BP2c.239+11842T>C (p.=)
c.50+9701T>C (p.=)
c.-106+9701T>C (p.=)
c.178+13472T>C (p.=)
c.35+11842T>C (p.=)
c.-170+13472T>C (p.=)
gnomAD
3g.185811315delCA903846233IGF2BP2c.239+11838del (p.=)
c.50+9697del (p.=)
c.-106+9697del (p.=)
c.178+13468del (p.=)
c.35+11838del (p.=)
c.-170+13468del (p.=)
dbSNP
3g.185811316T>CCA89824958IGF2BP2c.239+11837A>G (p.=)
c.50+9696A>G (p.=)
c.-106+9696A>G (p.=)
c.178+13467A>G (p.=)
c.35+11837A>G (p.=)
c.-170+13467A>G (p.=)
dbSNP gnomAD
3g.185811321C>TCA548611058IGF2BP2c.239+11832G>A (p.=)
c.50+9691G>A (p.=)
c.-106+9691G>A (p.=)
c.178+13462G>A (p.=)
c.35+11832G>A (p.=)
c.-170+13462G>A (p.=)
gnomAD
3g.185811324_185811327delCA917087318IGF2BP2c.239+11822_239+11825del (p.=)
c.50+9681_50+9684del (p.=)
c.-106+9681_-106+9684del (p.=)
c.178+13452_178+13455del (p.=)
c.35+11822_35+11825del (p.=)
c.-170+13452_-170+13455del (p.=)
dbSNP
3g.185811328C>GCA89824959IGF2BP2c.239+11825G>C (p.=)
c.50+9684G>C (p.=)
c.-106+9684G>C (p.=)
c.178+13455G>C (p.=)
c.35+11825G>C (p.=)
c.-170+13455G>C (p.=)
dbSNP gnomAD
3g.185811328C>TCA1057348963IGF2BP2c.239+11825G>A (p.=)
c.50+9684G>A (p.=)
c.-106+9684G>A (p.=)
c.178+13455G>A (p.=)
c.35+11825G>A (p.=)
c.-170+13455G>A (p.=)
3g.185811330C>GCA903846236IGF2BP2c.239+11823G>C (p.=)
c.50+9682G>C (p.=)
c.-106+9682G>C (p.=)
c.178+13453G>C (p.=)
c.35+11823G>C (p.=)
c.-170+13453G>C (p.=)
3g.185811331A>GCA903846237IGF2BP2c.239+11822T>C (p.=)
c.50+9681T>C (p.=)
c.-106+9681T>C (p.=)
c.178+13452T>C (p.=)
c.35+11822T>C (p.=)
c.-170+13452T>C (p.=)
3g.185811332T>CCA89824960IGF2BP2c.239+11821A>G (p.=)
c.50+9680A>G (p.=)
c.-106+9680A>G (p.=)
c.178+13451A>G (p.=)
c.35+11821A>G (p.=)
c.-170+13451A>G (p.=)
dbSNP
3g.185811336C>TCA903846238IGF2BP2c.239+11817G>A (p.=)
c.50+9676G>A (p.=)
c.-106+9676G>A (p.=)
c.178+13447G>A (p.=)
c.35+11817G>A (p.=)
c.-170+13447G>A (p.=)
3g.185811339G>CCA89824961IGF2BP2c.239+11814C>G (p.=)
c.50+9673C>G (p.=)
c.-106+9673C>G (p.=)
c.178+13444C>G (p.=)
c.35+11814C>G (p.=)
c.-170+13444C>G (p.=)
dbSNP gnomAD
3g.185811340C>TCA1057348976IGF2BP2c.239+11813G>A (p.=)
c.50+9672G>A (p.=)
c.-106+9672G>A (p.=)
c.178+13443G>A (p.=)
c.35+11813G>A (p.=)
c.-170+13443G>A (p.=)
3g.185811341C>GCA89824962IGF2BP2c.239+11812G>C (p.=)
c.50+9671G>C (p.=)
c.-106+9671G>C (p.=)
c.178+13442G>C (p.=)
c.35+11812G>C (p.=)
c.-170+13442G>C (p.=)
dbSNP
3g.185811344T>CCA1057348979IGF2BP2c.239+11809A>G (p.=)
c.50+9668A>G (p.=)
c.-106+9668A>G (p.=)
c.178+13439A>G (p.=)
c.35+11809A>G (p.=)
c.-170+13439A>G (p.=)
3g.185811345G>ACA89824963IGF2BP2c.239+11808C>T (p.=)
c.50+9667C>T (p.=)
c.-106+9667C>T (p.=)
c.178+13438C>T (p.=)
c.35+11808C>T (p.=)
c.-170+13438C>T (p.=)
dbSNP
3g.185811346T>GCA89824964IGF2BP2c.239+11807A>C (p.=)
c.50+9666A>C (p.=)
c.-106+9666A>C (p.=)
c.178+13437A>C (p.=)
c.35+11807A>C (p.=)
c.-170+13437A>C (p.=)
dbSNP
3g.185811351G>ACA1057348981IGF2BP2c.239+11802C>T (p.=)
c.50+9661C>T (p.=)
c.-106+9661C>T (p.=)
c.178+13432C>T (p.=)
c.35+11802C>T (p.=)
c.-170+13432C>T (p.=)
3g.185811352G>ACA89824965IGF2BP2c.239+11801C>T (p.=)
c.50+9660C>T (p.=)
c.-106+9660C>T (p.=)
c.178+13431C>T (p.=)
c.35+11801C>T (p.=)
c.-170+13431C>T (p.=)
dbSNP
3g.185811359delCA1057348983IGF2BP2c.239+11792del (p.=)
c.50+9651del (p.=)
c.-106+9651del (p.=)
c.178+13422del (p.=)
c.35+11792del (p.=)
c.-170+13422del (p.=)
3g.185811361A>GCA548611150IGF2BP2c.239+11792T>C (p.=)
c.50+9651T>C (p.=)
c.-106+9651T>C (p.=)
c.178+13422T>C (p.=)
c.35+11792T>C (p.=)
c.-170+13422T>C (p.=)
gnomAD
3g.185811363A>GCA903846239IGF2BP2c.239+11790T>C (p.=)
c.50+9649T>C (p.=)
c.-106+9649T>C (p.=)
c.178+13420T>C (p.=)
c.35+11790T>C (p.=)
c.-170+13420T>C (p.=)
3g.185811372A>GCA903846240IGF2BP2c.239+11781T>C (p.=)
c.50+9640T>C (p.=)
c.-106+9640T>C (p.=)
c.178+13411T>C (p.=)
c.35+11781T>C (p.=)
c.-170+13411T>C (p.=)
3g.185811373G>CCA1057348990IGF2BP2c.239+11780C>G (p.=)
c.50+9639C>G (p.=)
c.-106+9639C>G (p.=)
c.178+13410C>G (p.=)
c.35+11780C>G (p.=)
c.-170+13410C>G (p.=)
3g.185811382A>CCA1057349040IGF2BP2c.239+11771T>G (p.=)
c.50+9630T>G (p.=)
c.-106+9630T>G (p.=)
c.178+13401T>G (p.=)
c.35+11771T>G (p.=)
c.-170+13401T>G (p.=)
3g.185811382A>GCA89824966IGF2BP2c.239+11771T>C (p.=)
c.50+9630T>C (p.=)
c.-106+9630T>C (p.=)
c.178+13401T>C (p.=)
c.35+11771T>C (p.=)
c.-170+13401T>C (p.=)
dbSNP
3g.185811382A>TCA89824967IGF2BP2c.239+11771T>A (p.=)
c.50+9630T>A (p.=)
c.-106+9630T>A (p.=)
c.178+13401T>A (p.=)
c.35+11771T>A (p.=)
c.-170+13401T>A (p.=)
dbSNP
3g.185811384A>GCA903846242IGF2BP2c.239+11769T>C (p.=)
c.50+9628T>C (p.=)
c.-106+9628T>C (p.=)
c.178+13399T>C (p.=)
c.35+11769T>C (p.=)
c.-170+13399T>C (p.=)
3g.185811386T>ACA11462588IGF2BP2c.239+11767A>T (p.=)
c.50+9626A>T (p.=)
c.-106+9626A>T (p.=)
c.178+13397A>T (p.=)
c.35+11767A>T (p.=)
c.-170+13397A>T (p.=)
dbSNP gnomAD

Number of alleles fetched