ClinVar Miner

List of variants in gene GLI3 studied for not provided

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Gene type:
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Total variants: 71
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HGVS dbSNP
GRCh37/hg19 7p14.1(chr7:42156923-42225427)x1
GRCh37/hg19 7p14.1(chr7:42255311-42634746)x3
NM_000168.5(GLI3):c.1076T>G (p.Met359Arg) rs1437242698
NM_000168.5(GLI3):c.1111G>C (p.Gly371Arg) rs143523044
NM_000168.5(GLI3):c.1182A>G (p.Pro394=) rs748606221
NM_000168.5(GLI3):c.1191_1206del16 (p.Thr398Serfs) rs1554315071
NM_000168.5(GLI3):c.1346G>C (p.Arg449Pro) rs745809543
NM_000168.5(GLI3):c.1357-17C>G rs190600888
NM_000168.5(GLI3):c.1357-3C>T rs886043679
NM_000168.5(GLI3):c.1393G>C (p.Gly465Arg) rs35488756
NM_000168.5(GLI3):c.1452G>A (p.Trp484Ter) rs1554314595
NM_000168.5(GLI3):c.1485G>A (p.Glu495=) rs149248727
NM_000168.5(GLI3):c.1498-6C>A rs754600966
NM_000168.5(GLI3):c.1578delC (p.Phe527Serfs) rs1064793685
NM_000168.5(GLI3):c.1697delA (p.His566Profs) rs886039667
NM_000168.5(GLI3):c.1812+3A>T rs796064500
NM_000168.5(GLI3):c.1959G>A (p.Pro653=) rs148226583
NM_000168.5(GLI3):c.1969G>A (p.Gly657Ser) rs377579354
NM_000168.5(GLI3):c.2032G>T (p.Asp678Tyr) rs1554306039
NM_000168.5(GLI3):c.2071C>T (p.Gln691Ter) rs1554306031
NM_000168.5(GLI3):c.2119C>T (p.Pro707Ser) rs121917716
NM_000168.5(GLI3):c.2165A>G (p.Asn722Ser) rs146130351
NM_000168.5(GLI3):c.2179G>A (p.Gly727Arg) rs121917710
NM_000168.5(GLI3):c.2200G>A (p.Asp734Asn) rs140479817
NM_000168.5(GLI3):c.223C>G (p.Pro75Ala) rs369237977
NM_000168.5(GLI3):c.2245A>G (p.Ile749Val) rs140048578
NM_000168.5(GLI3):c.2331C>T (p.His777=) rs1057524835
NM_000168.5(GLI3):c.2374C>T (p.Arg792Ter) rs121917714
NM_000168.5(GLI3):c.2419C>T (p.Leu807Phe) rs886039381
NM_000168.5(GLI3):c.241G>A (p.Glu81Lys) rs376725882
NM_000168.5(GLI3):c.2424A>G (p.Ile808Met) rs62622373
NM_000168.5(GLI3):c.2540G>A (p.Arg847Lys) rs143406263
NM_000168.5(GLI3):c.2585G>A (p.Arg862His) rs1206529384
NM_000168.5(GLI3):c.2635G>A (p.Ala879Thr) rs137939155
NM_000168.5(GLI3):c.2652C>T (p.Gly884=) rs886042483
NM_000168.5(GLI3):c.2826G>T (p.Pro942=) rs34245321
NM_000168.5(GLI3):c.2901delC (p.Val968Trpfs) rs1064796278
NM_000168.5(GLI3):c.2993C>T (p.Pro998Leu) rs929387
NM_000168.5(GLI3):c.29C>A (p.Thr10Asn) rs1554341697
NM_000168.5(GLI3):c.3118G>A (p.Glu1040Lys) rs772839719
NM_000168.5(GLI3):c.3147C>G (p.Tyr1049Ter) rs779898173
NM_000168.5(GLI3):c.3208A>T (p.Thr1070Ser) rs150907867
NM_000168.5(GLI3):c.3351G>A (p.Pro1117=) rs368061722
NM_000168.5(GLI3):c.341G>A (p.Arg114Lys) rs146458902
NM_000168.5(GLI3):c.3598C>G (p.His1200Asp) rs145069572
NM_000168.5(GLI3):c.3762T>C (p.Tyr1254=) rs148043302
NM_000168.5(GLI3):c.3771delT (p.Leu1258Serfs) rs1554304508
NM_000168.5(GLI3):c.3829C>G (p.Gln1277Glu) rs146582871
NM_000168.5(GLI3):c.3903A>G (p.Pro1301=) rs758771584
NM_000168.5(GLI3):c.3935T>G (p.Met1312Arg) rs199875457
NM_000168.5(GLI3):c.4145G>A (p.Gly1382Asp) rs1064796822
NM_000168.5(GLI3):c.4349T>G (p.Phe1450Cys) rs886042309
NM_000168.5(GLI3):c.4431dupT (p.Glu1478Terfs) rs1057520063
NM_000168.5(GLI3):c.444C>T (p.Tyr148=) rs142241970
NM_000168.5(GLI3):c.4560G>A (p.Ser1520=) rs79625212
NM_000168.5(GLI3):c.4606T>A (p.Ser1536Thr) rs75313224
NM_000168.5(GLI3):c.4619C>A (p.Thr1540Lys) rs748031460
NM_000168.5(GLI3):c.4665dupC (p.Asn1556Glnfs) rs1554304247
NM_000168.5(GLI3):c.547A>G (p.Thr183Ala) rs846266
NM_000168.5(GLI3):c.648C>T (p.Ile216=) rs886043938
NM_000168.6(GLI3):c.1002T>A (p.Tyr334Ter)
NM_000168.6(GLI3):c.1008C>A (p.His336Gln)
NM_000168.6(GLI3):c.1464_1489dup (p.Leu497Argfs) rs1554314581
NM_000168.6(GLI3):c.2003C>G (p.Pro668Arg)
NM_000168.6(GLI3):c.2174A>C (p.Asn725Thr)
NM_000168.6(GLI3):c.2309C>T (p.Ala770Val)
NM_000168.6(GLI3):c.2881G>A (p.Gly961Arg)
NM_000168.6(GLI3):c.3756G>A (p.Pro1252=)
NM_000168.6(GLI3):c.4007_4009delGGGinsAGT (p.Gly1336_Ala1337delinsGluSer)
NM_000168.6(GLI3):c.4036_4045dup (p.Ser1349Argfs)
NM_000168.6(GLI3):c.4317C>A (p.Tyr1439Ter)

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