ClinVar Miner

List of variants in gene GLI3 studied for not provided

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Gene type:
ClinVar version:
Total variants: 141
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HGVS dbSNP
GRCh37/hg19 7p14.1(chr7:42156923-42225427)x1
GRCh37/hg19 7p14.1(chr7:42174178-42319482)x3
GRCh37/hg19 7p14.1(chr7:42255311-42634746)x3
NC_000007.13:g.42007664del rs57654200
NC_000007.14:g.42223444del rs11366795
NM_000168.6(GLI3):c.1002T>A (p.Tyr334Ter) rs760303531
NM_000168.6(GLI3):c.1008C>A (p.His336Gln) rs1562698465
NM_000168.6(GLI3):c.1028+281G>T rs846322
NM_000168.6(GLI3):c.1028+3A>T rs368499795
NM_000168.6(GLI3):c.1029-22dup rs559579130
NM_000168.6(GLI3):c.1062C>T (p.Pro354=) rs1446107833
NM_000168.6(GLI3):c.1076T>G (p.Met359Arg) rs1437242698
NM_000168.6(GLI3):c.1111G>C (p.Gly371Arg) rs143523044
NM_000168.6(GLI3):c.1182A>G (p.Pro394=) rs748606221
NM_000168.6(GLI3):c.1191_1206del (p.Thr398fs) rs1554315071
NM_000168.6(GLI3):c.1206C>T (p.Pro402=) rs774831772
NM_000168.6(GLI3):c.1222G>A (p.Gly408Ser) rs200411081
NM_000168.6(GLI3):c.124+10A>G rs112576935
NM_000168.6(GLI3):c.125-263A>G rs846374
NM_000168.6(GLI3):c.1346G>C (p.Arg449Pro) rs745809543
NM_000168.6(GLI3):c.1356+10C>T rs765591867
NM_000168.6(GLI3):c.1356+64C>A rs78554970
NM_000168.6(GLI3):c.1357-17C>G rs190600888
NM_000168.6(GLI3):c.1357-3C>T rs886043679
NM_000168.6(GLI3):c.1357-4T>C rs1583801312
NM_000168.6(GLI3):c.1357-9T>A rs1583801330
NM_000168.6(GLI3):c.1393G>C (p.Gly465Arg) rs35488756
NM_000168.6(GLI3):c.1452G>A (p.Trp484Ter) rs1554314595
NM_000168.6(GLI3):c.1462_1497+2dup
NM_000168.6(GLI3):c.1464_1489dup (p.Leu497fs) rs1554314581
NM_000168.6(GLI3):c.1485G>A (p.Glu495=) rs149248727
NM_000168.6(GLI3):c.1497+1G>A
NM_000168.6(GLI3):c.1497+256C>T rs10248828
NM_000168.6(GLI3):c.1498-6C>A rs754600966
NM_000168.6(GLI3):c.1578del (p.Phe527fs) rs1064793685
NM_000168.6(GLI3):c.1647+226C>A rs4724086
NM_000168.6(GLI3):c.168C>T (p.Asn56=) rs376845825
NM_000168.6(GLI3):c.1697del (p.His566fs) rs886039667
NM_000168.6(GLI3):c.1728C>T (p.Tyr576=) rs35128755
NM_000168.6(GLI3):c.1800G>A (p.Thr600=) rs138445547
NM_000168.6(GLI3):c.1812+3A>T rs796064500
NM_000168.6(GLI3):c.1874G>A (p.Arg625Gln) rs1554306094
NM_000168.6(GLI3):c.1959G>A (p.Pro653=) rs148226583
NM_000168.6(GLI3):c.1969G>A (p.Gly657Ser) rs377579354
NM_000168.6(GLI3):c.2003C>G (p.Pro668Arg) rs143009880
NM_000168.6(GLI3):c.2032G>T (p.Asp678Tyr) rs1554306039
NM_000168.6(GLI3):c.2071C>T (p.Gln691Ter) rs1554306031
NM_000168.6(GLI3):c.2119C>T (p.Pro707Ser) rs121917716
NM_000168.6(GLI3):c.2165A>G (p.Asn722Ser) rs146130351
NM_000168.6(GLI3):c.2174A>C (p.Asn725Thr) rs749807129
NM_000168.6(GLI3):c.2179G>A (p.Gly727Arg) rs121917710
NM_000168.6(GLI3):c.2200G>A (p.Asp734Asn) rs140479817
NM_000168.6(GLI3):c.2232C>A (p.Ile744=) rs772276953
NM_000168.6(GLI3):c.223C>G (p.Pro75Ala) rs369237977
NM_000168.6(GLI3):c.2245A>G (p.Ile749Val) rs140048578
NM_000168.6(GLI3):c.2307G>A (p.Pro769=) rs766163765
NM_000168.6(GLI3):c.2309C>T (p.Ala770Val) rs144772281
NM_000168.6(GLI3):c.2331C>T (p.His777=) rs1057524835
NM_000168.6(GLI3):c.2374C>T (p.Arg792Ter) rs121917714
NM_000168.6(GLI3):c.2419C>T (p.Leu807Phe) rs886039381
NM_000168.6(GLI3):c.241G>A (p.Glu81Lys) rs376725882
NM_000168.6(GLI3):c.2424A>G (p.Ile808Met) rs62622373
NM_000168.6(GLI3):c.2431+123G>A rs4724083
NM_000168.6(GLI3):c.2432-5T>C rs768250382
NM_000168.6(GLI3):c.252A>G (p.Ser84=) rs1051536881
NM_000168.6(GLI3):c.2540G>A (p.Arg847Lys) rs143406263
NM_000168.6(GLI3):c.2585G>A (p.Arg862His) rs1206529384
NM_000168.6(GLI3):c.2604G>C (p.Ser868=) rs758273867
NM_000168.6(GLI3):c.2625C>G (p.Arg875=) rs949898100
NM_000168.6(GLI3):c.2635G>A (p.Ala879Thr) rs137939155
NM_000168.6(GLI3):c.2652C>T (p.Gly884=) rs886042483
NM_000168.6(GLI3):c.2697C>T (p.Ser899=) rs772034729
NM_000168.6(GLI3):c.2706C>T (p.Ala902=) rs779103816
NM_000168.6(GLI3):c.2826G>T (p.Pro942=) rs34245321
NM_000168.6(GLI3):c.2881G>A (p.Gly961Arg) rs745986297
NM_000168.6(GLI3):c.2901del (p.Val968fs) rs1064796278
NM_000168.6(GLI3):c.2993C>T (p.Pro998Leu) rs929387
NM_000168.6(GLI3):c.29C>A (p.Thr10Asn) rs1554341697
NM_000168.6(GLI3):c.3024G>A (p.Pro1008=) rs753894499
NM_000168.6(GLI3):c.3054G>A (p.Leu1018=) rs1022587271
NM_000168.6(GLI3):c.30C>T (p.Thr10=) rs148154157
NM_000168.6(GLI3):c.3118G>A (p.Glu1040Lys) rs772839719
NM_000168.6(GLI3):c.3141G>A (p.Gln1047=) rs201820452
NM_000168.6(GLI3):c.3147C>G (p.Tyr1049Ter) rs779898173
NM_000168.6(GLI3):c.3183C>G (p.His1061Gln) rs565428084
NM_000168.6(GLI3):c.3208A>T (p.Thr1070Ser) rs150907867
NM_000168.6(GLI3):c.3261C>T (p.Asn1087=) rs370714837
NM_000168.6(GLI3):c.3351G>A (p.Pro1117=) rs368061722
NM_000168.6(GLI3):c.3372C>T (p.His1124=)
NM_000168.6(GLI3):c.3405A>T (p.Pro1135=) rs1562658413
NM_000168.6(GLI3):c.341G>A (p.Arg114Lys) rs146458902
NM_000168.6(GLI3):c.3579C>T (p.Phe1193=) rs1583729785
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.368-248C>T rs17172004
NM_000168.6(GLI3):c.3756G>A (p.Pro1252=) rs758155716
NM_000168.6(GLI3):c.3756G>C (p.Pro1252=) rs758155716
NM_000168.6(GLI3):c.3762T>C (p.Tyr1254=) rs148043302
NM_000168.6(GLI3):c.3771del (p.Leu1258fs) rs1554304508
NM_000168.6(GLI3):c.3780G>A (p.Arg1260=) rs374477953
NM_000168.6(GLI3):c.3829C>G (p.Gln1277Glu) rs146582871
NM_000168.6(GLI3):c.3903A>G (p.Pro1301=) rs758771584
NM_000168.6(GLI3):c.3935T>G (p.Met1312Arg) rs199875457
NM_000168.6(GLI3):c.3986G>T (p.Gly1329Val) rs1583728660
NM_000168.6(GLI3):c.4007_4009delinsAGT (p.Gly1336_Ala1337delinsGluSer) rs1562657448
NM_000168.6(GLI3):c.4010del (p.Ala1337fs) rs1583728570
NM_000168.6(GLI3):c.4037_4046dup (p.Ser1349delinsArgAlaAspTer) rs1562657370
NM_000168.6(GLI3):c.4089C>T (p.Cys1363=) rs202059951
NM_000168.6(GLI3):c.4145G>A (p.Gly1382Asp) rs1064796822
NM_000168.6(GLI3):c.4245C>T (p.Thr1415=) rs201470312
NM_000168.6(GLI3):c.4317C>A (p.Tyr1439Ter) rs1562656975
NM_000168.6(GLI3):c.4349T>G (p.Phe1450Cys) rs886042309
NM_000168.6(GLI3):c.4356G>A (p.Gln1452=) rs377535957
NM_000168.6(GLI3):c.4431dup (p.Glu1478Ter) rs1057520063
NM_000168.6(GLI3):c.444C>T (p.Tyr148=) rs142241970
NM_000168.6(GLI3):c.4560G>A (p.Ser1520=) rs79625212
NM_000168.6(GLI3):c.4606T>A (p.Ser1536Thr) rs75313224
NM_000168.6(GLI3):c.4619C>A (p.Thr1540Lys) rs748031460
NM_000168.6(GLI3):c.4629G>A (p.Ala1543=) rs975131125
NM_000168.6(GLI3):c.4638A>T (p.Pro1546=) rs1233172983
NM_000168.6(GLI3):c.4665dup (p.Asn1556fs) rs1554304247
NM_000168.6(GLI3):c.4698G>A (p.Leu1566=) rs905011458
NM_000168.6(GLI3):c.474-6A>G rs778136455
NM_000168.6(GLI3):c.480C>T (p.Ser160=) rs148660482
NM_000168.6(GLI3):c.501G>A (p.Thr167=) rs149901929
NM_000168.6(GLI3):c.546C>A (p.Pro182=) rs751666907
NM_000168.6(GLI3):c.547A>G (p.Thr183Ala) rs846266
NM_000168.6(GLI3):c.558C>T (p.Ser186=) rs769275169
NM_000168.6(GLI3):c.565C>T (p.Pro189Ser) rs201940674
NM_000168.6(GLI3):c.567C>T (p.Pro189=) rs371984494
NM_000168.6(GLI3):c.600C>T (p.Tyr200=) rs755703829
NM_000168.6(GLI3):c.633A>G (p.Pro211=) rs769152784
NM_000168.6(GLI3):c.636G>A (p.Ser212=) rs369422937
NM_000168.6(GLI3):c.648C>T (p.Ile216=) rs886043938
NM_000168.6(GLI3):c.680-14_680-13del rs759633765
NM_000168.6(GLI3):c.825T>C (p.Asp275=) rs201269781
NM_000168.6(GLI3):c.826+255T>C rs699492
NM_000168.6(GLI3):c.827-181C>T rs73688623
NM_000168.6(GLI3):c.936G>T (p.Thr312=) rs200965295
NM_000168.6(GLI3):c.963C>T (p.Leu321=) rs34965132
NM_000168.6(GLI3):c.974G>A (p.Arg325His) rs781356257

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