Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.2148819C>TCA216262112IGF2,INS-IGF2c.-249+307G>A (p.=)
c.407+307G>A (p.=)
n.466+307G>A
n.612+307G>A
dbSNP
11g.2148820T>ACA216262117IGF2,INS-IGF2c.-249+306A>T (p.=)
c.407+306A>T (p.=)
n.466+306A>T
n.612+306A>T
dbSNP
11g.2148821C>TCA216262118IGF2,INS-IGF2c.-249+305G>A (p.=)
c.407+305G>A (p.=)
n.466+305G>A
n.612+305G>A
dbSNP gnomAD
11g.2148822C>TCA674546511IGF2,INS-IGF2c.-249+304G>A (p.=)
c.407+304G>A (p.=)
n.466+304G>A
n.612+304G>A
11g.2148823T>CCA653928190IGF2,INS-IGF2c.-249+303A>G (p.=)
c.407+303A>G (p.=)
n.466+303A>G
n.612+303A>G
COSMIC
11g.2148823T>GCA674546536IGF2,INS-IGF2c.-249+303A>C (p.=)
c.407+303A>C (p.=)
n.466+303A>C
n.612+303A>C
11g.2148824C>GCA597087540IGF2,INS-IGF2c.-249+302G>C (p.=)
c.407+302G>C (p.=)
n.466+302G>C
n.612+302G>C
gnomAD
11g.2148827C>TCA597087541IGF2,INS-IGF2c.-249+299G>A (p.=)
c.407+299G>A (p.=)
n.466+299G>A
n.612+299G>A
gnomAD
11g.2148828T>GCA674546544IGF2,INS-IGF2c.-249+298A>C (p.=)
c.407+298A>C (p.=)
n.466+298A>C
n.612+298A>C
11g.2148829A>GCA674546546IGF2,INS-IGF2c.-249+297T>C (p.=)
c.407+297T>C (p.=)
n.466+297T>C
n.612+297T>C
11g.2148829A>TCA597087542IGF2,INS-IGF2c.-249+297T>A (p.=)
c.407+297T>A (p.=)
n.466+297T>A
n.612+297T>A
gnomAD
11g.2148830C>TCA216262119IGF2,INS-IGF2c.-249+296G>A (p.=)
c.407+296G>A (p.=)
n.466+296G>A
n.612+296G>A
dbSNP
11g.2148833dupCA674546549IGF2,INS-IGF2c.-249+296dup (p.=)
c.407+296dup (p.=)
n.466+296dup
n.612+296dup
dbSNP
11g.2148839delCA597087543IGF2,INS-IGF2c.-249+284del (p.=)
c.407+284del (p.=)
n.466+284del
n.612+284del
dbSNP gnomAD
11g.2148843G>ACA934421633IGF2,INS-IGF2c.-249+283C>T (p.=)
c.407+283C>T (p.=)
n.466+283C>T
n.612+283C>T
11g.2148848G>ACA674546553IGF2,INS-IGF2c.-249+278C>T (p.=)
c.407+278C>T (p.=)
n.466+278C>T
n.612+278C>T
11g.2148857T>ACA216262122IGF2,INS-IGF2c.-249+269A>T (p.=)
c.407+269A>T (p.=)
n.466+269A>T
n.612+269A>T
dbSNP
11g.2148858C>TCA216262126IGF2,INS-IGF2c.-249+268G>A (p.=)
c.407+268G>A (p.=)
n.466+268G>A
n.612+268G>A
dbSNP
11g.2148866dupCA674546556IGF2,INS-IGF2c.-249+263dup (p.=)
c.407+263dup (p.=)
n.466+263dup
n.612+263dup
dbSNP
11g.2148867C>ACA597087544IGF2,INS-IGF2c.-249+259G>T (p.=)
c.407+259G>T (p.=)
n.466+259G>T
n.612+259G>T
gnomAD
11g.2148867C>GCA674546558IGF2,INS-IGF2c.-249+259G>C (p.=)
c.407+259G>C (p.=)
n.466+259G>C
n.612+259G>C
11g.2148869T>GCA674546560IGF2,INS-IGF2c.-249+257A>C (p.=)
c.407+257A>C (p.=)
n.466+257A>C
n.612+257A>C
11g.2148870A>GCA597087545IGF2,INS-IGF2c.-249+256T>C (p.=)
c.407+256T>C (p.=)
n.466+256T>C
n.612+256T>C
gnomAD
11g.2148872T>ACA216262129IGF2,INS-IGF2c.-249+254A>T (p.=)
c.407+254A>T (p.=)
n.466+254A>T
n.612+254A>T
dbSNP gnomAD
11g.2148874T>CCA597087546IGF2,INS-IGF2c.-249+252A>G (p.=)
c.407+252A>G (p.=)
n.466+252A>G
n.612+252A>G
gnomAD
11g.2148878T>CCA597087547IGF2,INS-IGF2c.-249+248A>G (p.=)
c.407+248A>G (p.=)
n.466+248A>G
n.612+248A>G
gnomAD
11g.2148884A>CCA597087548IGF2,INS-IGF2c.-249+242T>G (p.=)
c.407+242T>G (p.=)
n.466+242T>G
n.612+242T>G
gnomAD
11g.2148885_2148887delCA216262132IGF2,INS-IGF2c.-249+239_-249+241del (p.=)
c.407+239_407+241del (p.=)
n.466+239_466+241del
n.612+239_612+241del
dbSNP
11g.2148886C>ACA597087549IGF2,INS-IGF2c.-249+240G>T (p.=)
c.407+240G>T (p.=)
n.466+240G>T
n.612+240G>T
gnomAD
11g.2148886C>TCA674546595IGF2,INS-IGF2c.-249+240G>A (p.=)
c.407+240G>A (p.=)
n.466+240G>A
n.612+240G>A
11g.2148887C>TCA674546614IGF2,INS-IGF2c.-249+239G>A (p.=)
c.407+239G>A (p.=)
n.466+239G>A
n.612+239G>A
11g.2148890A>CCA674546619IGF2,INS-IGF2c.-249+236T>G (p.=)
c.407+236T>G (p.=)
n.466+236T>G
n.612+236T>G
11g.2148895C>TCA674546623IGF2,INS-IGF2c.-249+231G>A (p.=)
c.407+231G>A (p.=)
n.466+231G>A
n.612+231G>A
11g.2148898T>CCA597087550IGF2,INS-IGF2c.-249+228A>G (p.=)
c.407+228A>G (p.=)
n.466+228A>G
n.612+228A>G
gnomAD
11g.2148900T>CCA674546630IGF2,INS-IGF2c.-249+226A>G (p.=)
c.407+226A>G (p.=)
n.466+226A>G
n.612+226A>G
11g.2148904G>ACA216262144IGF2,INS-IGF2c.-249+222C>T (p.=)
c.407+222C>T (p.=)
n.466+222C>T
n.612+222C>T
dbSNP
11g.2148911A>GCA597087551IGF2,INS-IGF2c.-249+215T>C (p.=)
c.407+215T>C (p.=)
n.466+215T>C
n.612+215T>C
gnomAD
11g.2148912G>CCA674546641IGF2,INS-IGF2c.-249+214C>G (p.=)
c.407+214C>G (p.=)
n.466+214C>G
n.612+214C>G
11g.2148913G>ACA15711014IGF2,INS-IGF2c.-249+213C>T (p.=)
c.407+213C>T (p.=)
n.466+213C>T
n.612+213C>T
dbSNP gnomAD

Number of alleles fetched