Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.2148913G>ACA15711014IGF2,INS-IGF2c.-249+213C>T (p.=)
c.407+213C>T (p.=)
n.466+213C>T
n.612+213C>T
dbSNP gnomAD
11g.2148919C>ACA216262151IGF2,INS-IGF2c.-249+207G>T (p.=)
c.407+207G>T (p.=)
n.466+207G>T
n.612+207G>T
dbSNP
11g.2148919C>GCA674546646IGF2,INS-IGF2c.-249+207G>C (p.=)
c.407+207G>C (p.=)
n.466+207G>C
n.612+207G>C
11g.2148919C>TCA216262155IGF2,INS-IGF2c.-249+207G>A (p.=)
c.407+207G>A (p.=)
n.466+207G>A
n.612+207G>A
dbSNP
11g.2148922C>TCA674546648IGF2,INS-IGF2c.-249+204G>A (p.=)
c.407+204G>A (p.=)
n.466+204G>A
n.612+204G>A
11g.2148923T>CCA674546650IGF2,INS-IGF2c.-249+203A>G (p.=)
c.407+203A>G (p.=)
n.466+203A>G
n.612+203A>G
11g.2148927C>GCA216262159IGF2,INS-IGF2c.-249+199G>C (p.=)
c.407+199G>C (p.=)
n.466+199G>C
n.612+199G>C
dbSNP
11g.2148928A>GCA934421648IGF2,INS-IGF2c.-249+198T>C (p.=)
c.407+198T>C (p.=)
n.466+198T>C
n.612+198T>C
11g.2148929A>GCA216262163IGF2,INS-IGF2c.-249+197T>C (p.=)
c.407+197T>C (p.=)
n.466+197T>C
n.612+197T>C
dbSNP
11g.2148932G>ACA216262164IGF2,INS-IGF2c.-249+194C>T (p.=)
c.407+194C>T (p.=)
n.466+194C>T
n.612+194C>T
dbSNP gnomAD
11g.2148938C>TCA934421650IGF2,INS-IGF2c.-249+188G>A (p.=)
c.407+188G>A (p.=)
n.466+188G>A
n.478G>A
n.612+188G>A
11g.2148939C>TCA216262165IGF2,INS-IGF2c.-249+187G>A (p.=)
c.407+187G>A (p.=)
n.466+187G>A
n.477G>A
n.612+187G>A
dbSNP
11g.2148942C>TCA934421653IGF2,INS-IGF2c.-249+184G>A (p.=)
c.407+184G>A (p.=)
n.466+184G>A
n.474G>A
n.612+184G>A
11g.2148944C>TCA216262168IGF2,INS-IGF2c.-249+182G>A (p.=)
c.407+182G>A (p.=)
n.466+182G>A
n.472G>A
n.612+182G>A
dbSNP gnomAD
11g.2148945A>GCA216262171IGF2,INS-IGF2c.-249+181T>C (p.=)
c.407+181T>C (p.=)
n.466+181T>C
n.471T>C
n.612+181T>C
dbSNP gnomAD
11g.2148949C>TCA597087552IGF2,INS-IGF2c.-249+177G>A (p.=)
c.407+177G>A (p.=)
n.466+177G>A
n.467G>A
n.612+177G>A
gnomAD
11g.2148954C>GCA597087553IGF2,INS-IGF2c.-249+172G>C (p.=)
c.407+172G>C (p.=)
n.466+172G>C
n.462G>C
n.612+172G>C
gnomAD
11g.2148959G>ACA674546688IGF2,INS-IGF2c.-249+167C>T (p.=)
c.407+167C>T (p.=)
n.466+167C>T
n.457C>T
n.612+167C>T
11g.2148959G>CCA216262187IGF2,INS-IGF2c.-249+167C>G (p.=)
c.407+167C>G (p.=)
n.466+167C>G
n.457C>G
n.612+167C>G
dbSNP gnomAD
11g.2148962G>TCA597087554IGF2,INS-IGF2c.-249+164C>A (p.=)
c.407+164C>A (p.=)
n.466+164C>A
n.454C>A
n.612+164C>A
gnomAD
11g.2148964G>ACA216262190IGF2,INS-IGF2c.-249+162C>T (p.=)
c.407+162C>T (p.=)
n.466+162C>T
n.452C>T
n.612+162C>T
dbSNP
11g.2148965G>CCA597087555IGF2,INS-IGF2c.-249+161C>G (p.=)
c.407+161C>G (p.=)
n.466+161C>G
n.451C>G
n.612+161C>G
gnomAD
11g.2148966C>TCA216262193IGF2,INS-IGF2c.-249+160G>A (p.=)
c.407+160G>A (p.=)
n.466+160G>A
n.450G>A
n.612+160G>A
dbSNP
11g.2148973C>GCA216262197IGF2,INS-IGF2c.-249+153G>C (p.=)
c.407+153G>C (p.=)
n.466+153G>C
n.443G>C
n.612+153G>C
dbSNP
11g.2148976G>ACA216262201IGF2,INS-IGF2c.-249+150C>T (p.=)
c.407+150C>T (p.=)
n.466+150C>T
n.440C>T
n.612+150C>T
dbSNP gnomAD
11g.2148978G>ACA597087556IGF2,INS-IGF2c.-249+148C>T (p.=)
c.407+148C>T (p.=)
n.466+148C>T
n.438C>T
n.612+148C>T
gnomAD
11g.2148979G>TCA597087557IGF2,INS-IGF2c.-249+147C>A (p.=)
c.407+147C>A (p.=)
n.466+147C>A
n.437C>A
n.612+147C>A
gnomAD
11g.2148980C>TCA934421666IGF2,INS-IGF2c.-249+146G>A (p.=)
c.407+146G>A (p.=)
n.466+146G>A
n.436G>A
n.612+146G>A
11g.2148983C>ACA216262212IGF2,INS-IGF2c.-249+143G>T (p.=)
c.407+143G>T (p.=)
n.466+143G>T
n.433G>T
n.612+143G>T
dbSNP gnomAD
11g.2148985C>ACA674546708IGF2,INS-IGF2c.-249+141G>T (p.=)
c.407+141G>T (p.=)
n.466+141G>T
n.431G>T
n.612+141G>T
11g.2148985C>TCA216262215IGF2,INS-IGF2c.-249+141G>A (p.=)
c.407+141G>A (p.=)
n.466+141G>A
n.431G>A
n.612+141G>A
dbSNP
11g.2148987G>ACA934421671IGF2,INS-IGF2c.-249+139C>T (p.=)
c.407+139C>T (p.=)
n.466+139C>T
n.429C>T
n.612+139C>T
11g.2148988C>TCA216262219IGF2,INS-IGF2c.-249+138G>A (p.=)
c.407+138G>A (p.=)
n.466+138G>A
n.428G>A
n.612+138G>A
dbSNP gnomAD
11g.2148991_2148993delCA934421675IGF2,INS-IGF2c.-249+131_-249+133del (p.=)
c.407+131_407+133del (p.=)
n.466+131_466+133del
n.421_423del
n.612+131_612+133del
11g.2148992C>TCA934421676IGF2,INS-IGF2c.-249+134G>A (p.=)
c.407+134G>A (p.=)
n.466+134G>A
n.424G>A
n.612+134G>A
11g.2148993T>CCA597087558IGF2,INS-IGF2c.-249+133A>G (p.=)
c.407+133A>G (p.=)
n.466+133A>G
n.423A>G
n.612+133A>G
gnomAD

Number of alleles fetched