NM_000168.6(GLI3):c.1356+11G>C
|
rs846273
|
0.97240
|
NM_000168.6(GLI3):c.547A>G (p.Thr183Ala)
|
rs846266
|
0.64495
|
NM_000168.6(GLI3):c.2993C>T (p.Pro998Leu)
|
rs929387
|
0.31467
|
NM_000168.6(GLI3):c.1498-44G>A
|
rs17707162
|
0.08936
|
NM_000168.6(GLI3):c.900C>T (p.Ser300=)
|
rs35961850
|
0.07677
|
NM_000168.6(GLI3):c.537C>T (p.His179=)
|
rs3898405
|
0.07173
|
NM_000168.6(GLI3):c.4071C>T (p.Tyr1357=)
|
rs34089404
|
0.07043
|
NM_000168.6(GLI3):c.*30G>T
|
rs77886553
|
0.03497
|
NM_000168.6(GLI3):c.4609C>T (p.Arg1537Cys)
|
rs35364414
|
0.03460
|
NM_000168.6(GLI3):c.4007G>A (p.Gly1336Glu)
|
rs35280470
|
0.03456
|
NM_000168.6(GLI3):c.2835G>C (p.Leu945=)
|
rs61758978
|
0.01858
|
NM_000168.6(GLI3):c.3774C>G (p.Leu1258=)
|
rs35448119
|
0.01377
|
NM_000168.6(GLI3):c.3083G>T (p.Ser1028Ile)
|
rs79049330
|
0.01304
|
NM_000168.6(GLI3):c.3084C>T (p.Ser1028=)
|
rs79703713
|
0.01303
|
NM_000168.6(GLI3):c.1029-7C>T
|
rs78280303
|
0.01279
|
NM_000168.6(GLI3):c.1029-11C>T
|
rs116195563
|
0.00867
|
NM_000168.6(GLI3):c.368-19G>A
|
rs79879393
|
0.00858
|
NM_000168.6(GLI3):c.2802G>A (p.Ala934=)
|
rs61730503
|
0.00520
|
NM_000168.6(GLI3):c.2165A>G (p.Asn722Ser)
|
rs146130351
|
0.00514
|
NM_000168.6(GLI3):c.2104-50C>T
|
rs115463742
|
0.00406
|
NM_000168.6(GLI3):c.1393G>C (p.Gly465Arg)
|
rs35488756
|
0.00320
|
NM_000168.6(GLI3):c.2373G>A (p.Pro791=)
|
rs61754622
|
0.00267
|
NM_000168.6(GLI3):c.1357-17C>G
|
rs190600888
|
0.00256
|
NM_000168.6(GLI3):c.840C>G (p.Ser280=)
|
rs77084911
|
0.00198
|
NM_000168.6(GLI3):c.1243-40A>C
|
rs77659679
|
0.00163
|
NM_000168.6(GLI3):c.679+40C>A
|
rs367979286
|
0.00157
|
NM_000168.6(GLI3):c.1813-47G>A
|
rs199956247
|
0.00114
|
NM_000168.6(GLI3):c.680-25C>T
|
rs55872291
|
0.00110
|
NM_000168.6(GLI3):c.1242+25C>T
|
rs375904354
|
0.00013
|
NM_000168.6(GLI3):c.*11A>G
|
rs139896177
|
0.00011
|
NM_000168.6(GLI3):c.2432-30C>T
|
rs374365217
|
0.00011
|
NM_000168.6(GLI3):c.3894G>A (p.Pro1298=)
|
rs530418832
|
0.00006
|
NM_000168.6(GLI3):c.2184C>T (p.Leu728=)
|
rs149724824
|
0.00005
|
NM_000168.6(GLI3):c.3540G>A (p.Gly1180=)
|
rs143551701
|
0.00004
|
NM_000168.6(GLI3):c.3772C>G (p.Leu1258Val)
|
rs754908186
|
0.00003
|
NM_000168.6(GLI3):c.659G>A (p.Arg220His)
|
rs747805984
|
0.00003
|
NM_000168.6(GLI3):c.743G>A (p.Arg248His)
|
rs186337909
|
0.00002
|
NM_000168.6(GLI3):c.3312C>T (p.Asn1104=)
|
rs770842648
|
0.00001
|
NM_000168.6(GLI3):c.*15dup
|
rs886038264
|
|
NM_000168.6(GLI3):c.1029-22dup
|
rs559579130
|
|
NM_000168.6(GLI3):c.1242+42C>G
|
rs772766325
|
|
NM_000168.6(GLI3):c.1369G>A (p.Gly457Arg)
|
|
|
NM_000168.6(GLI3):c.1448_1463dup (p.Arg489fs)
|
|
|
NM_000168.6(GLI3):c.1463C>T (p.Ala488Val)
|
|
|
NM_000168.6(GLI3):c.1509C>T (p.Asn503=)
|
rs34020684
|
|
NM_000168.6(GLI3):c.1570C>A (p.Gln524Lys)
|
|
|
NM_000168.6(GLI3):c.1777C>A (p.Arg593Ser)
|
|
|
NM_000168.6(GLI3):c.1864A>C (p.Ser622Arg)
|
|
|
NM_000168.6(GLI3):c.1894C>T (p.His632Tyr)
|
|
|
NM_000168.6(GLI3):c.1911T>C (p.His637=)
|
rs886038265
|
|
NM_000168.6(GLI3):c.1927C>T (p.Arg643Ter)
|
rs121917709
|
|
NM_000168.6(GLI3):c.2482C>T (p.Pro828Ser)
|
|
|
NM_000168.6(GLI3):c.2488A>G (p.Arg830Gly)
|
|
|
NM_000168.6(GLI3):c.2501C>G (p.Ser834Cys)
|
|
|
NM_000168.6(GLI3):c.2584C>T (p.Arg862Cys)
|
|
|
NM_000168.6(GLI3):c.2610C>A (p.Cys870Ter)
|
|
|
NM_000168.6(GLI3):c.2664_2676del (p.Asn888fs)
|
|
|
NM_000168.6(GLI3):c.2692A>G (p.Ile898Val)
|
|
|
NM_000168.6(GLI3):c.2826G>C (p.Pro942=)
|
rs34245321
|
|
NM_000168.6(GLI3):c.3001G>A (p.Gly1001Ser)
|
rs202182779
|
|
NM_000168.6(GLI3):c.3092A>G (p.Asn1031Ser)
|
|
|
NM_000168.6(GLI3):c.3523del (p.Ser1175fs)
|
|
|
NM_000168.6(GLI3):c.3638A>G (p.Tyr1213Cys)
|
|
|
NM_000168.6(GLI3):c.3706G>A (p.Gly1236Arg)
|
|
|
NM_000168.6(GLI3):c.371CTC[1] (p.Pro125del)
|
|
|
NM_000168.6(GLI3):c.3751G>T (p.Ala1251Ser)
|
|
|
NM_000168.6(GLI3):c.4020C>T (p.Pro1340=)
|
rs35139358
|
|
NM_000168.6(GLI3):c.4168G>A (p.Gly1390Arg)
|
|
|
NM_000168.6(GLI3):c.4317C>G (p.Tyr1439Ter)
|
|
|
NM_000168.6(GLI3):c.4392C>A (p.Asp1464Glu)
|
|
|
NM_000168.6(GLI3):c.4559C>T (p.Ser1520Leu)
|
|
|
NM_000168.6(GLI3):c.4621_4625dup (p.Ala1543fs)
|
|
|
NM_000168.6(GLI3):c.528C>G (p.Ile176Met)
|
rs539622820
|
|
NM_000168.6(GLI3):c.669C>G (p.Ser223Arg)
|
|
|
NM_000168.6(GLI3):c.758A>T (p.Asp253Val)
|
|
|