ClinVar Miner

List of variants in gene GLI3 studied for not specified

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Gene type:
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Total variants: 88
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HGVS dbSNP
NM_000168.6(GLI3):c.*11A>G rs139896177
NM_000168.6(GLI3):c.*15dup rs886038264
NM_000168.6(GLI3):c.*30G>T rs77886553
NM_000168.6(GLI3):c.1029-11C>T rs116195563
NM_000168.6(GLI3):c.1029-22dup rs559579130
NM_000168.6(GLI3):c.1029-7C>T rs78280303
NM_000168.6(GLI3):c.1182A>G (p.Pro394=) rs748606221
NM_000168.6(GLI3):c.1207G>A (p.Val403Ile) rs201070431
NM_000168.6(GLI3):c.124+10A>G rs112576935
NM_000168.6(GLI3):c.1242+16C>T rs754808194
NM_000168.6(GLI3):c.1242+25C>T rs375904354
NM_000168.6(GLI3):c.1242+42C>G rs772766325
NM_000168.6(GLI3):c.1242+8G>A rs75925934
NM_000168.6(GLI3):c.1243-40A>C rs77659679
NM_000168.6(GLI3):c.1287G>A (p.Pro429=) rs760816574
NM_000168.6(GLI3):c.1356+11G>C rs846273
NM_000168.6(GLI3):c.1357-17C>G rs190600888
NM_000168.6(GLI3):c.1393G>C (p.Gly465Arg) rs35488756
NM_000168.6(GLI3):c.1498-44G>A rs17707162
NM_000168.6(GLI3):c.1509C>T (p.Asn503=) rs34020684
NM_000168.6(GLI3):c.1593T>C (p.Tyr531=) rs749798195
NM_000168.6(GLI3):c.1647+13G>A rs149955824
NM_000168.6(GLI3):c.1671C>T (p.Tyr557=) rs143948870
NM_000168.6(GLI3):c.1813-47G>A rs199956247
NM_000168.6(GLI3):c.1911T>C (p.His637=) rs886038265
NM_000168.6(GLI3):c.2006C>T (p.Thr669Ile) rs139108417
NM_000168.6(GLI3):c.2104-50C>T rs115463742
NM_000168.6(GLI3):c.2104-8C>T rs769769944
NM_000168.6(GLI3):c.2119C>T (p.Pro707Ser) rs121917716
NM_000168.6(GLI3):c.211G>A (p.Val71Ile) rs143843875
NM_000168.6(GLI3):c.2165A>G (p.Asn722Ser) rs146130351
NM_000168.6(GLI3):c.2179G>A (p.Gly727Arg) rs121917710
NM_000168.6(GLI3):c.2184C>T (p.Leu728=) rs149724824
NM_000168.6(GLI3):c.2245A>G (p.Ile749Val) rs140048578
NM_000168.6(GLI3):c.2373G>A (p.Pro791=) rs61754622
NM_000168.6(GLI3):c.2424A>G (p.Ile808Met) rs62622373
NM_000168.6(GLI3):c.2432-30C>T rs374365217
NM_000168.6(GLI3):c.2802G>A (p.Ala934=) rs61730503
NM_000168.6(GLI3):c.280C>T (p.Leu94=) rs115137047
NM_000168.6(GLI3):c.2826G>C (p.Pro942=) rs34245321
NM_000168.6(GLI3):c.2835G>C (p.Leu945=) rs61758978
NM_000168.6(GLI3):c.2993C>T (p.Pro998Leu) rs929387
NM_000168.6(GLI3):c.3001G>A (p.Gly1001Ser) rs202182779
NM_000168.6(GLI3):c.3015C>T (p.Ala1005=) rs200965852
NM_000168.6(GLI3):c.3083G>T (p.Ser1028Ile) rs79049330
NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile) rs886043721
NM_000168.6(GLI3):c.3084C>T (p.Ser1028=) rs79703713
NM_000168.6(GLI3):c.3098C>A (p.Pro1033Gln) rs376956433
NM_000168.6(GLI3):c.3119A>T (p.Glu1040Val) rs376477553
NM_000168.6(GLI3):c.313C>T (p.Arg105Cys) rs555794809
NM_000168.6(GLI3):c.3140_3141delinsCA (p.Gln1047Pro) rs1064796326
NM_000168.6(GLI3):c.3208A>T (p.Thr1070Ser) rs150907867
NM_000168.6(GLI3):c.3284A>G (p.Asp1095Gly) rs1554304659
NM_000168.6(GLI3):c.3312C>T (p.Asn1104=) rs770842648
NM_000168.6(GLI3):c.341G>A (p.Arg114Lys) rs146458902
NM_000168.6(GLI3):c.3453C>T (p.Pro1151=) rs749508811
NM_000168.6(GLI3):c.3540G>A (p.Gly1180=) rs143551701
NM_000168.6(GLI3):c.3598C>G (p.His1200Asp) rs145069572
NM_000168.6(GLI3):c.363C>T (p.His121=) rs150295615
NM_000168.6(GLI3):c.3664C>T (p.Pro1222Ser) rs118149040
NM_000168.6(GLI3):c.368-19G>A rs79879393
NM_000168.6(GLI3):c.3695A>C (p.His1232Pro) rs780924905
NM_000168.6(GLI3):c.3772C>G (p.Leu1258Val) rs754908186
NM_000168.6(GLI3):c.3774C>G (p.Leu1258=) rs35448119
NM_000168.6(GLI3):c.3829C>G (p.Gln1277Glu) rs146582871
NM_000168.6(GLI3):c.3894G>A (p.Pro1298=) rs530418832
NM_000168.6(GLI3):c.3970G>C (p.Ala1324Pro) rs1480007692
NM_000168.6(GLI3):c.3984C>T (p.Leu1328=) rs148940743
NM_000168.6(GLI3):c.3987C>T (p.Gly1329=) rs145859702
NM_000168.6(GLI3):c.4005G>A (p.Pro1335=) rs149860242
NM_000168.6(GLI3):c.4007G>A (p.Gly1336Glu) rs35280470
NM_000168.6(GLI3):c.4020C>T (p.Pro1340=) rs35139358
NM_000168.6(GLI3):c.4071C>T (p.Tyr1357=) rs34089404
NM_000168.6(GLI3):c.411T>C (p.Ile137=) rs200203051
NM_000168.6(GLI3):c.444C>T (p.Tyr148=) rs142241970
NM_000168.6(GLI3):c.4609C>T (p.Arg1537Cys) rs35364414
NM_000168.6(GLI3):c.474-4C>T rs74536326
NM_000168.6(GLI3):c.501G>A (p.Thr167=) rs149901929
NM_000168.6(GLI3):c.528C>G (p.Ile176Met) rs539622820
NM_000168.6(GLI3):c.537C>T (p.His179=) rs3898405
NM_000168.6(GLI3):c.547A>G (p.Thr183Ala) rs846266
NM_000168.6(GLI3):c.563C>A (p.Ser188Tyr) rs369926331
NM_000168.6(GLI3):c.679+40C>A rs367979286
NM_000168.6(GLI3):c.680-10C>T rs1035936832
NM_000168.6(GLI3):c.680-25C>T rs55872291
NM_000168.6(GLI3):c.743G>A (p.Arg248His) rs186337909
NM_000168.6(GLI3):c.840C>G (p.Ser280=) rs77084911
NM_000168.6(GLI3):c.900C>T (p.Ser300=) rs35961850

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