ClinVar Miner

List of variants in gene GLI3 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP
NM_000168.5(GLI3):c.1029-16dupT rs559579130
NM_000168.6(GLI3):c.*11A>G rs139896177
NM_000168.6(GLI3):c.*15dup rs886038264
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.1243-40A>C rs77659679
NM_000168.6(GLI3):c.1287G>A (p.Pro429=) rs760816574
NM_000168.6(GLI3):c.1357-17C>G rs190600888
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.211G>A (p.Val71Ile) rs143843875
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.280C>T (p.Leu94=) rs115137047
NM_000168.6(GLI3):c.3001G>A (p.Gly1001Ser) rs202182779
NM_000168.6(GLI3):c.3119A>T (p.Glu1040Val) rs376477553
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.3695A>C (p.His1232Pro) rs780924905
NM_000168.6(GLI3):c.3772C>G (p.Leu1258Val) rs754908186
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.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.411T>C (p.Ile137=) rs200203051
NM_000168.6(GLI3):c.444C>T (p.Tyr148=) rs142241970
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.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

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