| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.2148819C>T | CA216262112 | IGF2,INS-IGF2 | c.-249+307G>A (p.=) c.407+307G>A (p.=) n.466+307G>A n.612+307G>A | dbSNP |
| 11 | g.2148820T>A | CA216262117 | IGF2,INS-IGF2 | c.-249+306A>T (p.=) c.407+306A>T (p.=) n.466+306A>T n.612+306A>T | dbSNP |
| 11 | g.2148821C>T | CA216262118 | IGF2,INS-IGF2 | c.-249+305G>A (p.=) c.407+305G>A (p.=) n.466+305G>A n.612+305G>A | dbSNP gnomAD |
| 11 | g.2148822C>T | CA674546511 | IGF2,INS-IGF2 | c.-249+304G>A (p.=) c.407+304G>A (p.=) n.466+304G>A n.612+304G>A | |
| 11 | g.2148823T>C | CA653928190 | IGF2,INS-IGF2 | c.-249+303A>G (p.=) c.407+303A>G (p.=) n.466+303A>G n.612+303A>G | COSMIC |
| 11 | g.2148823T>G | CA674546536 | IGF2,INS-IGF2 | c.-249+303A>C (p.=) c.407+303A>C (p.=) n.466+303A>C n.612+303A>C | |
| 11 | g.2148824C>G | CA597087540 | IGF2,INS-IGF2 | c.-249+302G>C (p.=) c.407+302G>C (p.=) n.466+302G>C n.612+302G>C | gnomAD |
| 11 | g.2148827C>T | CA597087541 | IGF2,INS-IGF2 | c.-249+299G>A (p.=) c.407+299G>A (p.=) n.466+299G>A n.612+299G>A | gnomAD |
| 11 | g.2148828T>G | CA674546544 | IGF2,INS-IGF2 | c.-249+298A>C (p.=) c.407+298A>C (p.=) n.466+298A>C n.612+298A>C | |
| 11 | g.2148829A>G | CA674546546 | IGF2,INS-IGF2 | c.-249+297T>C (p.=) c.407+297T>C (p.=) n.466+297T>C n.612+297T>C | |
| 11 | g.2148829A>T | CA597087542 | IGF2,INS-IGF2 | c.-249+297T>A (p.=) c.407+297T>A (p.=) n.466+297T>A n.612+297T>A | gnomAD |
| 11 | g.2148830C>T | CA216262119 | IGF2,INS-IGF2 | c.-249+296G>A (p.=) c.407+296G>A (p.=) n.466+296G>A n.612+296G>A | dbSNP |
| 11 | g.2148833dup | CA674546549 | IGF2,INS-IGF2 | c.-249+296dup (p.=) c.407+296dup (p.=) n.466+296dup n.612+296dup | dbSNP |
| 11 | g.2148839del | CA597087543 | IGF2,INS-IGF2 | c.-249+284del (p.=) c.407+284del (p.=) n.466+284del n.612+284del | dbSNP gnomAD |
| 11 | g.2148843G>A | CA934421633 | IGF2,INS-IGF2 | c.-249+283C>T (p.=) c.407+283C>T (p.=) n.466+283C>T n.612+283C>T | |
| 11 | g.2148848G>A | CA674546553 | IGF2,INS-IGF2 | c.-249+278C>T (p.=) c.407+278C>T (p.=) n.466+278C>T n.612+278C>T | |
| 11 | g.2148857T>A | CA216262122 | IGF2,INS-IGF2 | c.-249+269A>T (p.=) c.407+269A>T (p.=) n.466+269A>T n.612+269A>T | dbSNP |
| 11 | g.2148858C>T | CA216262126 | IGF2,INS-IGF2 | c.-249+268G>A (p.=) c.407+268G>A (p.=) n.466+268G>A n.612+268G>A | dbSNP |
| 11 | g.2148866dup | CA674546556 | IGF2,INS-IGF2 | c.-249+263dup (p.=) c.407+263dup (p.=) n.466+263dup n.612+263dup | dbSNP |
| 11 | g.2148867C>A | CA597087544 | IGF2,INS-IGF2 | c.-249+259G>T (p.=) c.407+259G>T (p.=) n.466+259G>T n.612+259G>T | gnomAD |
| 11 | g.2148867C>G | CA674546558 | IGF2,INS-IGF2 | c.-249+259G>C (p.=) c.407+259G>C (p.=) n.466+259G>C n.612+259G>C | |
| 11 | g.2148869T>G | CA674546560 | IGF2,INS-IGF2 | c.-249+257A>C (p.=) c.407+257A>C (p.=) n.466+257A>C n.612+257A>C | |
| 11 | g.2148870A>G | CA597087545 | IGF2,INS-IGF2 | c.-249+256T>C (p.=) c.407+256T>C (p.=) n.466+256T>C n.612+256T>C | gnomAD |
| 11 | g.2148872T>A | CA216262129 | IGF2,INS-IGF2 | c.-249+254A>T (p.=) c.407+254A>T (p.=) n.466+254A>T n.612+254A>T | dbSNP gnomAD |
| 11 | g.2148874T>C | CA597087546 | IGF2,INS-IGF2 | c.-249+252A>G (p.=) c.407+252A>G (p.=) n.466+252A>G n.612+252A>G | gnomAD |
| 11 | g.2148878T>C | CA597087547 | IGF2,INS-IGF2 | c.-249+248A>G (p.=) c.407+248A>G (p.=) n.466+248A>G n.612+248A>G | gnomAD |
| 11 | g.2148884A>C | CA597087548 | IGF2,INS-IGF2 | c.-249+242T>G (p.=) c.407+242T>G (p.=) n.466+242T>G n.612+242T>G | gnomAD |
| 11 | g.2148885_2148887del | CA216262132 | IGF2,INS-IGF2 | c.-249+239_-249+241del (p.=) c.407+239_407+241del (p.=) n.466+239_466+241del n.612+239_612+241del | dbSNP |
| 11 | g.2148886C>A | CA597087549 | IGF2,INS-IGF2 | c.-249+240G>T (p.=) c.407+240G>T (p.=) n.466+240G>T n.612+240G>T | gnomAD |
| 11 | g.2148886C>T | CA674546595 | IGF2,INS-IGF2 | c.-249+240G>A (p.=) c.407+240G>A (p.=) n.466+240G>A n.612+240G>A | |
| 11 | g.2148887C>T | CA674546614 | IGF2,INS-IGF2 | c.-249+239G>A (p.=) c.407+239G>A (p.=) n.466+239G>A n.612+239G>A | |
| 11 | g.2148890A>C | CA674546619 | IGF2,INS-IGF2 | c.-249+236T>G (p.=) c.407+236T>G (p.=) n.466+236T>G n.612+236T>G | |
| 11 | g.2148895C>T | CA674546623 | IGF2,INS-IGF2 | c.-249+231G>A (p.=) c.407+231G>A (p.=) n.466+231G>A n.612+231G>A | |
| 11 | g.2148898T>C | CA597087550 | IGF2,INS-IGF2 | c.-249+228A>G (p.=) c.407+228A>G (p.=) n.466+228A>G n.612+228A>G | gnomAD |
| 11 | g.2148900T>C | CA674546630 | IGF2,INS-IGF2 | c.-249+226A>G (p.=) c.407+226A>G (p.=) n.466+226A>G n.612+226A>G | |
| 11 | g.2148904G>A | CA216262144 | IGF2,INS-IGF2 | c.-249+222C>T (p.=) c.407+222C>T (p.=) n.466+222C>T n.612+222C>T | dbSNP |
| 11 | g.2148911A>G | CA597087551 | IGF2,INS-IGF2 | c.-249+215T>C (p.=) c.407+215T>C (p.=) n.466+215T>C n.612+215T>C | gnomAD |
| 11 | g.2148912G>C | CA674546641 | IGF2,INS-IGF2 | c.-249+214C>G (p.=) c.407+214C>G (p.=) n.466+214C>G n.612+214C>G | |
| 11 | g.2148913G>A | CA15711014 | IGF2,INS-IGF2 | c.-249+213C>T (p.=) c.407+213C>T (p.=) n.466+213C>T n.612+213C>T | dbSNP gnomAD |