ClinVar Miner

List of variants in gene GLI3 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_000168.6(GLI3):c.125-263A>G rs846374 0.98657
NM_000168.6(GLI3):c.1356+11G>C rs846273 0.97240
NM_000168.6(GLI3):c.-43+224G>C rs2302024 0.85866
NM_000168.6(GLI3):c.1028+281G>T rs846322 0.64985
NM_000168.6(GLI3):c.826+154T>C rs699493 0.64764
NM_000168.6(GLI3):c.547A>G (p.Thr183Ala) rs846266 0.64495
NM_000168.6(GLI3):c.679+124T>C rs846267 0.57384
NM_000168.6(GLI3):c.474-175T>G rs846265 0.56647
NM_000168.6(GLI3):c.826+255T>C rs699492 0.56647
NM_000168.6(GLI3):c.1647+226C>A rs4724086 0.50278
NM_000168.6(GLI3):c.2431+123G>A rs4724083 0.40087
NC_000007.14:g.41960903C>T rs66495651 0.33442
NM_000168.6(GLI3):c.2993C>T (p.Pro998Leu) rs929387 0.31467
NM_000168.6(GLI3):c.*2757C>T rs3823720 0.25562
NM_000168.6(GLI3):c.125-333G>T rs3801203 0.12761
NM_000168.6(GLI3):c.*265A>C rs201493390 0.08079
NM_000168.6(GLI3):c.827-181C>T rs73688623 0.07682
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.1356+64C>A rs78554970 0.06687
NM_000168.6(GLI3):c.2104-209T>G rs77170102 0.06486
NM_000168.6(GLI3):c.1497+256C>T rs10248828 0.06432
NM_000168.6(GLI3):c.827-204C>T rs846321 0.05993
NM_000168.6(GLI3):c.124+61C>A rs2286291 0.04453
NM_000168.6(GLI3):c.*248T>A rs61091998 0.04248
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.-42-11G>C rs80019165 0.03314
NM_000168.6(GLI3):c.1356+228G>A rs115359867 0.02406
NM_000168.6(GLI3):c.*249A>T rs6972450 0.02026
NM_000168.6(GLI3):c.2835G>C (p.Leu945=) rs61758978 0.01858
NM_000168.5(GLI3):c.*3392G>T rs115519476 0.01463
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.2802G>A (p.Ala934=) rs61730503 0.00520
NM_000168.6(GLI3):c.2165A>G (p.Asn722Ser) rs146130351 0.00514
NM_000168.6(GLI3):c.2179G>A (p.Gly727Arg) rs121917710 0.00511
NM_000168.6(GLI3):c.4510A>C (p.Ile1504Leu) rs145419251 0.00424
NM_000168.6(GLI3):c.341G>A (p.Arg114Lys) rs146458902 0.00274
NM_000168.6(GLI3):c.840C>G (p.Ser280=) rs77084911 0.00198
NM_000168.6(GLI3):c.2424A>G (p.Ile808Met) rs62622373 0.00194
NM_000168.6(GLI3):c.444C>T (p.Tyr148=) rs142241970 0.00191
NM_000168.6(GLI3):c.*2666G>A rs117987369 0.00142
NM_000168.6(GLI3):c.1671C>T (p.Tyr557=) rs143948870 0.00123
NM_000168.6(GLI3):c.*9A>G rs187024593 0.00093
NM_000168.6(GLI3):c.2245A>G (p.Ile749Val) rs140048578 0.00039
NM_000168.6(GLI3):c.3935T>G (p.Met1312Arg) rs199875457 0.00027
NM_000168.6(GLI3):c.3598C>G (p.His1200Asp) rs145069572 0.00025
NM_000168.6(GLI3):c.363C>T (p.His121=) rs150295615 0.00008
NM_000168.6(GLI3):c.*248dup rs5883809
NM_000168.6(GLI3):c.*265dup rs550264781
NM_000168.6(GLI3):c.*2859G>A
NM_000168.6(GLI3):c.*3341dup rs138425063
NM_000168.6(GLI3):c.-42-149del rs11366795
NM_000168.6(GLI3):c.-42-42del rs11266806
NM_000168.6(GLI3):c.-42-55dup rs11266806
NM_000168.6(GLI3):c.1029-22dup rs559579130
NM_000168.6(GLI3):c.1509C>T (p.Asn503=) rs34020684
NM_000168.6(GLI3):c.1648-220del rs60699625
NM_000168.6(GLI3):c.1648-230dup rs60699625
NM_000168.6(GLI3):c.2104-143del rs57654200
NM_000168.6(GLI3):c.2431+201dup rs34658310
NM_000168.6(GLI3):c.2826G>C (p.Pro942=) rs34245321
NM_000168.6(GLI3):c.3083_3084del (p.Ser1028fs) rs2128705914
NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile) rs886043721
NM_000168.6(GLI3):c.367+49TG[17] rs34148485
NM_000168.6(GLI3):c.367+49TG[18] rs34148485
NM_000168.6(GLI3):c.367+49TG[19] rs34148485
NM_000168.6(GLI3):c.367+49TG[20] rs34148485
NM_000168.6(GLI3):c.367+49TG[22] rs34148485
NM_000168.6(GLI3):c.367+90GC[4] rs199711555
NM_000168.6(GLI3):c.368-248C>T rs17172004
NM_000168.6(GLI3):c.4020C>T (p.Pro1340=) rs35139358
NM_000168.6(GLI3):c.679+156del rs144496307

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