ClinVar Miner

List of variants in gene GLI3 reported by Preventiongenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
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)

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