ClinVar Miner

List of variants in gene GLI3 reported as uncertain significance for Pallister-Hall syndrome

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP
NM_000168.6(GLI3):c.*1007G>A rs886062327
NM_000168.6(GLI3):c.*1027C>T rs886062326
NM_000168.6(GLI3):c.*1239T>A rs886062325
NM_000168.6(GLI3):c.*1263C>T rs886062324
NM_000168.6(GLI3):c.*1366C>T rs886062323
NM_000168.6(GLI3):c.*1386A>G rs886062322
NM_000168.6(GLI3):c.*1411G>A rs148318176
NM_000168.6(GLI3):c.*1471C>T rs886062321
NM_000168.6(GLI3):c.*165A>G rs886062333
NM_000168.6(GLI3):c.*1688C>G rs886062320
NM_000168.6(GLI3):c.*1780C>T rs886062319
NM_000168.6(GLI3):c.*1858C>T rs886062318
NM_000168.6(GLI3):c.*2146_*2150del rs774204684
NM_000168.6(GLI3):c.*2216T>C rs886062317
NM_000168.6(GLI3):c.*2257A>T rs886062316
NM_000168.6(GLI3):c.*2358del rs144064690
NM_000168.6(GLI3):c.*2419T>C rs886062315
NM_000168.6(GLI3):c.*2465G>C rs886062314
NM_000168.6(GLI3):c.*248del rs5883809
NM_000168.6(GLI3):c.*248dup rs5883809
NM_000168.6(GLI3):c.*2508G>C rs886062313
NM_000168.6(GLI3):c.*265A>C rs201493390
NM_000168.6(GLI3):c.*2666G>A rs117987369
NM_000168.6(GLI3):c.*266_*267insA rs1554304160
NM_000168.6(GLI3):c.*2676C>T rs886062312
NM_000168.6(GLI3):c.*3094T>C rs886062311
NM_000168.6(GLI3):c.*3369C>A rs886062310
NM_000168.6(GLI3):c.*512C>T rs886062330
NM_000168.6(GLI3):c.*589T>C rs886062329
NM_000168.6(GLI3):c.*66G>T rs886062334
NM_000168.6(GLI3):c.*911A>G rs187664615
NM_000168.6(GLI3):c.*974T>A rs886062328
NM_000168.6(GLI3):c.-3A>G rs886062340
NM_000168.6(GLI3):c.-47C>T rs886062341
NM_000168.6(GLI3):c.-78G>T rs886062342
NM_000168.6(GLI3):c.-83C>T rs886062343
NM_000168.6(GLI3):c.1207G>A (p.Val403Ile) rs201070431
NM_000168.6(GLI3):c.1462G>A (p.Ala488Thr) rs756581886
NM_000168.6(GLI3):c.1800G>A (p.Thr600=) rs138445547
NM_000168.6(GLI3):c.1845T>C (p.Thr615=) rs373687877
NM_000168.6(GLI3):c.1958C>T (p.Pro653Leu) rs141220299
NM_000168.6(GLI3):c.2412C>G (p.Val804=) rs761829250
NM_000168.6(GLI3):c.2493C>A (p.Ser831Arg) rs752838669
NM_000168.6(GLI3):c.2960A>G (p.Tyr987Cys) rs777313061
NM_000168.6(GLI3):c.3118G>A (p.Glu1040Lys) rs772839719
NM_000168.6(GLI3):c.3149C>T (p.Thr1050Met) rs146556791
NM_000168.6(GLI3):c.353T>C (p.Met118Thr) rs886062339
NM_000168.6(GLI3):c.3631G>A (p.Gly1211Arg) rs757059523
NM_000168.6(GLI3):c.367C>T (p.His123Tyr) rs199909375
NM_000168.6(GLI3):c.411T>C (p.Ile137=) rs200203051
NM_000168.6(GLI3):c.4296G>A (p.Leu1432=) rs768735366
NM_000168.6(GLI3):c.4356G>A (p.Gln1452=) rs377535957
NM_000168.6(GLI3):c.4590C>T (p.Asn1530=) rs886062335
NM_000168.6(GLI3):c.641C>T (p.Ser214Phe) rs886062338
NM_000168.6(GLI3):c.681G>A (p.Ala227=) rs752998397
NM_000168.6(GLI3):c.748C>T (p.Pro250Ser) rs202039538
NM_000168.6(GLI3):c.827-6T>C rs886062337
NM_000168.6(GLI3):c.961C>T (p.Leu321Phe) rs769956877
NM_000168.6(GLI3):c.99C>T (p.Ala33=) rs201109218

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