ClinVar Miner

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

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Gene type:
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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_000168.6(GLI3):c.2104-50C>T rs115463742 0.00406
NM_000168.6(GLI3):c.341G>A (p.Arg114Lys) rs146458902 0.00274
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.3664C>T (p.Pro1222Ser) rs118149040 0.00207
NM_000168.6(GLI3):c.840C>G (p.Ser280=) rs77084911 0.00198
NM_000168.6(GLI3):c.280C>T (p.Leu94=) rs115137047 0.00193
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.1671C>T (p.Tyr557=) rs143948870 0.00123
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.4005G>A (p.Pro1335=) rs149860242 0.00076
NM_000168.6(GLI3):c.2006C>T (p.Thr669Ile) rs139108417 0.00061
NM_000168.6(GLI3):c.3829C>G (p.Gln1277Glu) rs146582871 0.00043
NM_000168.6(GLI3):c.3987C>T (p.Gly1329=) rs145859702 0.00027
NM_000168.6(GLI3):c.124+10A>G rs112576935 0.00025
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.411T>C (p.Ile137=) rs200203051 0.00011
NM_000168.6(GLI3):c.1182A>G (p.Pro394=) rs748606221 0.00008
NM_000168.6(GLI3):c.363C>T (p.His121=) rs150295615 0.00008
NM_000168.6(GLI3):c.2184C>T (p.Leu728=) rs149724824 0.00005
NM_000168.6(GLI3):c.2104-8C>T rs769769944 0.00004
NM_000168.6(GLI3):c.3119A>T (p.Glu1040Val) rs376477553 0.00004
NM_000168.6(GLI3):c.3540G>A (p.Gly1180=) rs143551701 0.00004
NM_000168.6(GLI3):c.563C>A (p.Ser188Tyr) rs369926331 0.00004
NM_000168.6(GLI3):c.3772C>G (p.Leu1258Val) rs754908186 0.00003
NM_000168.6(GLI3):c.1242+16C>T rs754808194 0.00002
NM_000168.6(GLI3):c.743G>A (p.Arg248His) rs186337909 0.00002
NM_000168.6(GLI3):c.1287G>A (p.Pro429=) rs760816574 0.00001
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.1207G>A (p.Val403Ile) rs201070431
NM_000168.6(GLI3):c.1242+42C>G rs772766325
NM_000168.6(GLI3):c.1659C>T (p.Cys553=)
NM_000168.6(GLI3):c.1911T>C (p.His637=) rs886038265
NM_000168.6(GLI3):c.3001G>A (p.Gly1001Ser) rs202182779
NM_000168.6(GLI3):c.3453C>T (p.Pro1151=) rs749508811
NM_000168.6(GLI3):c.3695A>C (p.His1232Pro) rs780924905
NM_000168.6(GLI3):c.528C>G (p.Ile176Met) rs539622820
NM_000168.6(GLI3):c.680-10C>T rs1035936832

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