ClinVar Miner

List of variants in gene GLI2 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 151
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HGVS dbSNP gnomAD frequency
NM_001374353.1(GLI2):c.2939C>G (p.Pro980Arg) rs563818052 0.00088
NM_001374353.1(GLI2):c.607G>A (p.Ala203Thr) rs147044066 0.00088
NM_001374353.1(GLI2):c.1080G>A (p.Ser360=) rs149110951 0.00073
NM_001374353.1(GLI2):c.305G>A (p.Arg102Gln) rs148442092 0.00035
NM_001374353.1(GLI2):c.2251C>T (p.Leu751=) rs200831069 0.00033
NM_001374353.1(GLI2):c.4506C>T (p.Gly1502=) rs200499325 0.00020
NM_001374353.1(GLI2):c.132G>A (p.Ala44=) rs145778937 0.00017
NM_001374353.1(GLI2):c.189G>A (p.Pro63=) rs200471311 0.00016
NM_001374353.1(GLI2):c.221A>G (p.His74Arg) rs377700501 0.00016
NM_001374353.1(GLI2):c.4147G>T (p.Gly1383Cys) rs143914758 0.00013
NM_001374353.1(GLI2):c.2886G>A (p.Leu962=) rs777165274 0.00012
NM_001374353.1(GLI2):c.88A>C (p.Lys30Gln) rs201053024 0.00009
NM_001374353.1(GLI2):c.1875C>T (p.His625=) rs372341303 0.00007
NM_001374353.1(GLI2):c.1120C>T (p.Arg374Cys) rs200076785 0.00006
NM_001374353.1(GLI2):c.676C>T (p.Arg226Cys) rs758273853 0.00006
NM_001374353.1(GLI2):c.67G>A (p.Ala23Thr) rs201834541 0.00006
NM_001374353.1(GLI2):c.1701T>C (p.His567=) rs370382506 0.00005
NM_001374353.1(GLI2):c.4241C>T (p.Pro1414Leu) rs749402521 0.00005
NM_001374353.1(GLI2):c.4339G>A (p.Gly1447Arg) rs200274772 0.00005
NM_001374353.1(GLI2):c.2006C>T (p.Thr669Met) rs758298657 0.00004
NM_001374353.1(GLI2):c.2089G>A (p.Ala697Thr) rs553780090 0.00004
NM_001374353.1(GLI2):c.2132G>A (p.Arg711Gln) rs368549881 0.00004
NM_001374353.1(GLI2):c.4571C>A (p.Ser1524Tyr) rs199887024 0.00004
NM_001374353.1(GLI2):c.606C>T (p.Ser202=) rs146181686 0.00004
NM_001374353.1(GLI2):c.667G>A (p.Val223Met) rs1293201291 0.00004
NM_001374353.1(GLI2):c.1121G>A (p.Arg374His) rs370220133 0.00003
NM_001374353.1(GLI2):c.2107C>T (p.Arg703Cys) rs773976966 0.00003
NM_001374353.1(GLI2):c.2303A>T (p.Asn768Ile) rs768131638 0.00003
NM_001374353.1(GLI2):c.2503G>A (p.Ala835Thr) rs751028726 0.00003
NM_001374353.1(GLI2):c.4100G>A (p.Arg1367His) rs763852684 0.00003
NM_001374353.1(GLI2):c.4299G>T (p.Gln1433His) rs201523549 0.00003
NM_001374353.1(GLI2):c.1481C>T (p.Ser494Leu) rs372925840 0.00002
NM_001374353.1(GLI2):c.2075T>C (p.Leu692Pro) rs781438228 0.00002
NM_001374353.1(GLI2):c.451G>A (p.Ala151Thr) rs781771721 0.00002
NM_001374353.1(GLI2):c.515C>A (p.Thr172Asn) rs200720726 0.00002
NM_001374353.1(GLI2):c.661C>T (p.Pro221Ser) rs771675078 0.00002
NM_001374353.1(GLI2):c.1138G>A (p.Glu380Lys) rs374155310 0.00001
NM_001374353.1(GLI2):c.1153C>T (p.Arg385Trp) rs137925421 0.00001
NM_001374353.1(GLI2):c.1157C>T (p.Pro386Leu) rs757467621 0.00001
NM_001374353.1(GLI2):c.1349A>C (p.Lys450Thr) rs777526546 0.00001
NM_001374353.1(GLI2):c.1406C>T (p.Ala469Val) rs767030770 0.00001
NM_001374353.1(GLI2):c.152C>G (p.Pro51Arg) rs780172791 0.00001
NM_001374353.1(GLI2):c.196A>G (p.Met66Val) rs768282760 0.00001
NM_001374353.1(GLI2):c.2208G>A (p.Thr736=) rs372206751 0.00001
NM_001374353.1(GLI2):c.2365C>T (p.Arg789Cys) rs769667439 0.00001
NM_001374353.1(GLI2):c.2690G>A (p.Arg897Gln) rs886054813 0.00001
NM_001374353.1(GLI2):c.2884C>T (p.Leu962=) rs1345329176 0.00001
NM_001374353.1(GLI2):c.2948C>T (p.Pro983Leu) rs1348680961 0.00001
NM_001374353.1(GLI2):c.2957A>C (p.Asp986Ala) rs930268229 0.00001
NM_001374353.1(GLI2):c.3066C>T (p.Ala1022=) rs1472557461 0.00001
NM_001374353.1(GLI2):c.314C>T (p.Pro105Leu) rs370693310 0.00001
NM_001374353.1(GLI2):c.3784C>A (p.His1262Asn) rs794727100 0.00001
NM_001374353.1(GLI2):c.4294G>T (p.Gly1432Cys) rs746213496 0.00001
NM_001374353.1(GLI2):c.590G>A (p.Ser197Asn) rs556019545 0.00001
NM_001374353.1(GLI2):c.691C>T (p.Arg231Trp) rs781430951 0.00001
NM_001374353.1(GLI2):c.692G>A (p.Arg231Gln) rs756527906 0.00001
NM_001374353.1(GLI2):c.765G>A (p.Ser255=) rs200901345 0.00001
NM_001374353.1(GLI2):c.841C>A (p.Leu281Ile) rs1558923649 0.00001
NM_001374353.1(GLI2):c.879C>T (p.Pro293=) rs1318325355 0.00001
NM_001374353.1(GLI2):c.1046G>A (p.Ser349Asn)
NM_001374353.1(GLI2):c.1125C>T (p.Ser375=) rs1553475192
NM_001374353.1(GLI2):c.1166C>A (p.Pro389His)
NM_001374353.1(GLI2):c.1201A>G (p.Lys401Glu) rs2105036408
NM_001374353.1(GLI2):c.1218G>C (p.Arg406Ser) rs267598854
NM_001374353.1(GLI2):c.1244_1246delinsAGT (p.Val415_Val416delinsGluPhe)
NM_001374353.1(GLI2):c.1262A>G (p.Asn421Ser)
NM_001374353.1(GLI2):c.1366C>T (p.Arg456Cys)
NM_001374353.1(GLI2):c.1373A>G (p.Gln458Arg) rs1682566489
NM_001374353.1(GLI2):c.1384C>T (p.Arg462Trp) rs121917708
NM_001374353.1(GLI2):c.1447G>A (p.Glu483Lys)
NM_001374353.1(GLI2):c.1456_1457delinsTT (p.His486Phe) rs2105051287
NM_001374353.1(GLI2):c.1466C>T (p.Thr489Met)
NM_001374353.1(GLI2):c.1490A>C (p.Tyr497Ser) rs1553477146
NM_001374353.1(GLI2):c.1496G>A (p.Arg499His) rs1553477151
NM_001374353.1(GLI2):c.1505A>G (p.Asn502Ser) rs2105064232
NM_001374353.1(GLI2):c.1522C>T (p.Arg508Trp) rs2105064291
NM_001374353.1(GLI2):c.1523G>A (p.Arg508Gln)
NM_001374353.1(GLI2):c.1532C>A (p.Thr511Asn) rs2105064342
NM_001374353.1(GLI2):c.1588G>A (p.Ala530Thr)
NM_001374353.1(GLI2):c.1597C>T (p.Arg533Cys)
NM_001374353.1(GLI2):c.1639T>G (p.Tyr547Asp) rs1015526827
NM_001374353.1(GLI2):c.1738A>G (p.Lys580Glu)
NM_001374353.1(GLI2):c.1766G>A (p.Arg589His)
NM_001374353.1(GLI2):c.1771C>T (p.Pro591Ser) rs779910601
NM_001374353.1(GLI2):c.1890G>C (p.Lys630Asn) rs565184396
NM_001374353.1(GLI2):c.1897A>C (p.Ser633Arg)
NM_001374353.1(GLI2):c.1905+4A>G rs2105071708
NM_001374353.1(GLI2):c.193G>A (p.Asp65Asn)
NM_001374353.1(GLI2):c.2117T>C (p.Met706Thr)
NM_001374353.1(GLI2):c.2152_2154del (p.Glu718del) rs1682985936
NM_001374353.1(GLI2):c.2214C>A (p.Asn738Lys) rs904385464
NM_001374353.1(GLI2):c.2252T>C (p.Leu751Pro)
NM_001374353.1(GLI2):c.2291_2317del (p.Gly764_Ser772del) rs2105084733
NM_001374353.1(GLI2):c.2404G>A (p.Val802Met) rs985023327
NM_001374353.1(GLI2):c.2415C>T (p.Arg805=) rs886044110
NM_001374353.1(GLI2):c.2440_2442del (p.Ser815del) rs770837314
NM_001374353.1(GLI2):c.2449C>T (p.Arg817Cys)
NM_001374353.1(GLI2):c.2498G>C (p.Ser833Thr) rs1683093216
NM_001374353.1(GLI2):c.2569G>C (p.Gly857Arg)
NM_001374353.1(GLI2):c.2600C>T (p.Ala867Val) rs1485605591
NM_001374353.1(GLI2):c.2678G>T (p.Arg893Leu)
NM_001374353.1(GLI2):c.2681T>G (p.Met894Arg) rs1683106370
NM_001374353.1(GLI2):c.2765G>T (p.Arg922Leu)
NM_001374353.1(GLI2):c.2816C>T (p.Ala939Val)
NM_001374353.1(GLI2):c.2894C>A (p.Pro965Gln)
NM_001374353.1(GLI2):c.2934del (p.Gly979fs) rs2105089188
NM_001374353.1(GLI2):c.2995G>A (p.Asp999Asn)
NM_001374353.1(GLI2):c.299T>G (p.Leu100Trp)
NM_001374353.1(GLI2):c.3028C>T (p.Arg1010Trp) rs1404870952
NM_001374353.1(GLI2):c.3032C>T (p.Pro1011Leu)
NM_001374353.1(GLI2):c.3037A>G (p.Ser1013Gly) rs1553479006
NM_001374353.1(GLI2):c.3044G>A (p.Ser1015Asn)
NM_001374353.1(GLI2):c.3092G>T (p.Gly1031Val) rs1553479051
NM_001374353.1(GLI2):c.3116C>G (p.Pro1039Arg)
NM_001374353.1(GLI2):c.3124_3125delinsCT (p.Asp1042Leu) rs1553479074
NM_001374353.1(GLI2):c.3307T>C (p.Ser1103Pro) rs1246994636
NM_001374353.1(GLI2):c.3329G>A (p.Cys1110Tyr) rs1683160288
NM_001374353.1(GLI2):c.332G>A (p.Gly111Glu)
NM_001374353.1(GLI2):c.3367A>G (p.Asn1123Asp)
NM_001374353.1(GLI2):c.3370A>G (p.Asn1124Asp)
NM_001374353.1(GLI2):c.3379G>A (p.Val1127Met) rs1683163107
NM_001374353.1(GLI2):c.3414C>G (p.Asp1138Glu)
NM_001374353.1(GLI2):c.3418C>T (p.Leu1140=) rs141988240
NM_001374353.1(GLI2):c.3437C>T (p.Pro1146Leu)
NM_001374353.1(GLI2):c.3551C>G (p.Thr1184Arg)
NM_001374353.1(GLI2):c.355C>G (p.His119Asp)
NM_001374353.1(GLI2):c.3601A>G (p.Arg1201Gly) rs1573742574
NM_001374353.1(GLI2):c.3677C>T (p.Pro1226Leu) rs2105093808
NM_001374353.1(GLI2):c.3679C>T (p.His1227Tyr)
NM_001374353.1(GLI2):c.3822C>G (p.Asp1274Glu)
NM_001374353.1(GLI2):c.3877G>T (p.Ala1293Ser) rs2105094880
NM_001374353.1(GLI2):c.3950A>G (p.Gln1317Arg)
NM_001374353.1(GLI2):c.4025T>C (p.Met1342Thr)
NM_001374353.1(GLI2):c.403A>G (p.Ser135Gly)
NM_001374353.1(GLI2):c.4184C>G (p.Thr1395Arg)
NM_001374353.1(GLI2):c.41A>G (p.Glu14Gly) rs1684444560
NM_001374353.1(GLI2):c.4289A>G (p.Tyr1430Cys)
NM_001374353.1(GLI2):c.4300A>T (p.Ile1434Phe)
NM_001374353.1(GLI2):c.4307T>G (p.Met1436Arg)
NM_001374353.1(GLI2):c.4468G>T (p.Ala1490Ser)
NM_001374353.1(GLI2):c.582G>A (p.Leu194=) rs771191006
NM_001374353.1(GLI2):c.653T>G (p.Phe218Cys)
NM_001374353.1(GLI2):c.664C>G (p.Arg222Gly) rs763688196
NM_001374353.1(GLI2):c.665G>A (p.Arg222Gln) rs1213874652
NM_001374353.1(GLI2):c.686G>T (p.Arg229Leu)
NM_001374353.1(GLI2):c.71G>A (p.Gly24Asp)
NM_001374353.1(GLI2):c.833C>G (p.Ala278Gly)
NM_001374353.1(GLI2):c.836G>T (p.Gly279Val)
NM_001374353.1(GLI2):c.83_96del (p.Pro28fs)
NM_001374353.1(GLI2):c.871A>G (p.Ile291Val)
NM_001374353.1(GLI2):c.980A>G (p.Gln327Arg)

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