ClinVar Miner

List of variants in gene GLI3 reported as uncertain significance for Greig cephalopolysyndactyly syndrome

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Gene type:
ClinVar version:
Total variants: 85
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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.*1332C>T
NM_000168.6(GLI3):c.*1366C>T rs886062323
NM_000168.6(GLI3):c.*1386A>G rs886062322
NM_000168.6(GLI3):c.*1399T>C
NM_000168.6(GLI3):c.*1470A>C
NM_000168.6(GLI3):c.*1471C>T rs886062321
NM_000168.6(GLI3):c.*1553T>G
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.*185G>A rs531678760
NM_000168.6(GLI3):c.*2089G>A
NM_000168.6(GLI3):c.*2146_*2150del rs774204684
NM_000168.6(GLI3):c.*2176G>C
NM_000168.6(GLI3):c.*2216T>C rs886062317
NM_000168.6(GLI3):c.*2257A>T rs886062316
NM_000168.6(GLI3):c.*2276T>C rs568393106
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.*248T>A
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.*2517G>A
NM_000168.6(GLI3):c.*2612A>G
NM_000168.6(GLI3):c.*2620C>G rs56158069
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.*2744T>G
NM_000168.6(GLI3):c.*2861T>G
NM_000168.6(GLI3):c.*3002A>G
NM_000168.6(GLI3):c.*3094T>C rs886062311
NM_000168.6(GLI3):c.*311T>A
NM_000168.6(GLI3):c.*3309C>A rs553151369
NM_000168.6(GLI3):c.*333A>G
NM_000168.6(GLI3):c.*3369C>A rs886062310
NM_000168.6(GLI3):c.*386A>G
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.*73C>T
NM_000168.6(GLI3):c.*889T>C
NM_000168.6(GLI3):c.*974T>A rs886062328
NM_000168.6(GLI3):c.-105A>G
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.1057G>A (p.Ala353Thr)
NM_000168.6(GLI3):c.1066T>C (p.Ser356Pro)
NM_000168.6(GLI3):c.1343C>T (p.Ala448Val) rs912576738
NM_000168.6(GLI3):c.1540G>A (p.Val514Met)
NM_000168.6(GLI3):c.1648-7T>A
NM_000168.6(GLI3):c.1845T>C (p.Thr615=) rs373687877
NM_000168.6(GLI3):c.1957C>T (p.Pro653Ser)
NM_000168.6(GLI3):c.1958C>T (p.Pro653Leu) rs141220299
NM_000168.6(GLI3):c.2004G>A (p.Pro668=)
NM_000168.6(GLI3):c.21C>T (p.Ser7=)
NM_000168.6(GLI3):c.2375G>A (p.Arg792Gln)
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.2729G>A (p.Ser910Asn)
NM_000168.6(GLI3):c.2740G>A (p.Gly914Ser)
NM_000168.6(GLI3):c.3040G>C (p.Glu1014Gln)
NM_000168.6(GLI3):c.3065C>T (p.Pro1022Leu)
NM_000168.6(GLI3):c.3118G>A (p.Glu1040Lys) rs772839719
NM_000168.6(GLI3):c.3278C>T (p.Pro1093Leu)
NM_000168.6(GLI3):c.353T>C (p.Met118Thr) rs886062339
NM_000168.6(GLI3):c.3786A>G (p.Pro1262=)
NM_000168.6(GLI3):c.4016G>T (p.Arg1339Leu)
NM_000168.6(GLI3):c.4296G>A (p.Leu1432=) rs768735366
NM_000168.6(GLI3):c.4590C>T (p.Asn1530=) rs886062335
NM_000168.6(GLI3):c.4627G>T (p.Ala1543Ser)
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.776C>G (p.Ala259Gly)
NM_000168.6(GLI3):c.827-6T>C rs886062337

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