ClinVar Miner

List of variants in gene PLEC reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 89
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HGVS dbSNP
NM_000445.5(PLEC):c.10120G>A (p.Val3374Met) rs782748769
NM_000445.5(PLEC):c.10351G>A (p.Glu3451Lys) rs371846683
NM_000445.5(PLEC):c.10498G>A (p.Gly3500Ser) rs201765507
NM_000445.5(PLEC):c.10613G>A (p.Gly3538Asp) rs200972761
NM_000445.5(PLEC):c.10646C>T (p.Thr3549Met) rs375095764
NM_000445.5(PLEC):c.10825G>A (p.Gly3609Ser) rs202010719
NM_000445.5(PLEC):c.10882C>T (p.Arg3628Trp) rs782412400
NM_000445.5(PLEC):c.10912G>A (p.Gly3638Ser) rs201595670
NM_000445.5(PLEC):c.11006A>G (p.Tyr3669Cys) rs782531580
NM_000445.5(PLEC):c.11017C>T (p.Arg3673Cys) rs202175941
NM_000445.5(PLEC):c.11081G>T (p.Arg3694Leu) rs369798520
NM_000445.5(PLEC):c.11242C>T (p.Arg3748Cys) rs782134827
NM_000445.5(PLEC):c.12106C>T (p.Arg4036Cys) rs989279969
NM_000445.5(PLEC):c.12271G>A (p.Glu4091Lys) rs200206105
NM_000445.5(PLEC):c.12363C>T (p.Asn4121=) rs536268706
NM_000445.5(PLEC):c.12463C>T (p.Arg4155Trp) rs375335998
NM_000445.5(PLEC):c.12812G>A (p.Arg4271His) rs370769102
NM_000445.5(PLEC):c.128G>T (p.Gly43Val) rs781980239
NM_000445.5(PLEC):c.13022C>T (p.Ala4341Val) rs1057519154
NM_000445.5(PLEC):c.13058C>A (p.Thr4353Asn) rs1272806541
NM_000445.5(PLEC):c.13168C>T (p.Arg4390Cys) rs782348944
NM_000445.5(PLEC):c.13192G>A (p.Ala4398Thr) rs200361523
NM_000445.5(PLEC):c.13357C>T (p.Arg4453Cys) rs782043444
NM_000445.5(PLEC):c.1352G>A (p.Arg451Gln) rs199965040
NM_000445.5(PLEC):c.1442A>G (p.Asn481Ser) rs781981346
NM_000445.5(PLEC):c.1834G>A (p.Ala612Thr) rs368520468
NM_000445.5(PLEC):c.2044A>G (p.Lys682Glu) rs782382496
NM_000445.5(PLEC):c.2050A>T (p.Ser684Cys) rs199843296
NM_000445.5(PLEC):c.2060C>T (p.Ala687Val) rs782079821
NM_000445.5(PLEC):c.2087_2089AGA[2] (p.Lys698del) rs782157103
NM_000445.5(PLEC):c.2455G>A (p.Val819Met) rs782238465
NM_000445.5(PLEC):c.2470C>T (p.Arg824Cys) rs781813443
NM_000445.5(PLEC):c.2909C>T (p.Ala970Val) rs373846942
NM_000445.5(PLEC):c.292C>T (p.Arg98Cys) rs781901742
NM_000445.5(PLEC):c.3104G>A (p.Arg1035Gln) rs374666787
NM_000445.5(PLEC):c.3122A>G (p.Glu1041Gly) rs1554710940
NM_000445.5(PLEC):c.3379G>C (p.Gly1127Arg) rs201404741
NM_000445.5(PLEC):c.3541C>T (p.Arg1181Trp) rs782544250
NM_000445.5(PLEC):c.3572A>G (p.Gln1191Arg) rs782101451
NM_000445.5(PLEC):c.3757G>A (p.Ala1253Thr) rs782539707
NM_000445.5(PLEC):c.38A>C (p.Glu13Ala) rs370431965
NM_000445.5(PLEC):c.3923A>G (p.Asp1308Gly) rs782382295
NM_000445.5(PLEC):c.4216C>T (p.His1406Tyr) rs1554704116
NM_000445.5(PLEC):c.4404G>C (p.Glu1468Asp) rs782706697
NM_000445.5(PLEC):c.4420C>T (p.Arg1474Trp) rs782057352
NM_000445.5(PLEC):c.4432G>A (p.Glu1478Lys) rs868906137
NM_000445.5(PLEC):c.4445G>A (p.Arg1482His) rs542878693
NM_000445.5(PLEC):c.4729C>T (p.Arg1577Trp) rs560918806
NM_000445.5(PLEC):c.4801G>A (p.Ala1601Thr) rs914835478
NM_000445.5(PLEC):c.4825C>T (p.Arg1609Cys) rs782517203
NM_000445.5(PLEC):c.4867C>T (p.Leu1623=) rs782244301
NM_000445.5(PLEC):c.4911_4940dup (p.Arg1640_Arg1649dup) rs1554700573
NM_000445.5(PLEC):c.4936G>A (p.Glu1646Lys) rs782026068
NM_000445.5(PLEC):c.5027A>T (p.Glu1676Val) rs1554700070
NM_000445.5(PLEC):c.5093G>A (p.Arg1698His) rs782081177
NM_000445.5(PLEC):c.5329C>T (p.Arg1777Trp) rs782410213
NM_000445.5(PLEC):c.5396C>T (p.Ala1799Val) rs782439290
NM_000445.5(PLEC):c.5410_5411inv (p.Glu1804Ser) rs1554698316
NM_000445.5(PLEC):c.5412G>C (p.Glu1804Asp) rs774270631
NM_000445.5(PLEC):c.5471G>A (p.Arg1824His) rs782581787
NM_000445.5(PLEC):c.6279G>T (p.Gln2093His) rs201574539
NM_000445.5(PLEC):c.6545C>T (p.Ala2182Val) rs201922111
NM_000445.5(PLEC):c.6900G>A (p.Met2300Ile) rs1330572071
NM_000445.5(PLEC):c.7049C>T (p.Thr2350Met) rs550065687
NM_000445.5(PLEC):c.7294C>T (p.Arg2432Cys) rs782579294
NM_000445.5(PLEC):c.7415C>T (p.Ala2472Val) rs1020001131
NM_000445.5(PLEC):c.7426C>T (p.Arg2476Trp) rs571406033
NM_000445.5(PLEC):c.7464G>T (p.Lys2488Asn) rs371673069
NM_000445.5(PLEC):c.7618_7619delinsGC (p.Lys2540Ala) rs1554689196
NM_000445.5(PLEC):c.763C>T (p.Arg255Trp) rs200249446
NM_000445.5(PLEC):c.7687_7701del (p.Arg2563_Gln2567del) rs1554688820
NM_000445.5(PLEC):c.7714C>T (p.Arg2572Trp) rs782164998
NM_000445.5(PLEC):c.7753C>T (p.Arg2585Trp) rs961518883
NM_000445.5(PLEC):c.7777G>A (p.Val2593Met) rs782743395
NM_000445.5(PLEC):c.7811A>G (p.Glu2604Gly) rs549616678
NM_000445.5(PLEC):c.7903G>A (p.Ala2635Thr) rs199995144
NM_000445.5(PLEC):c.8122G>A (p.Glu2708Lys) rs200128670
NM_000445.5(PLEC):c.8360G>T (p.Gly2787Val) rs1554686155
NM_000445.5(PLEC):c.8401G>A (p.Val2801Ile) rs782359700
NM_000445.5(PLEC):c.8548C>T (p.Arg2850Cys) rs370334846
NM_000445.5(PLEC):c.8768A>G (p.Tyr2923Cys) rs375069554
NM_000445.5(PLEC):c.8896C>T (p.Arg2966Trp) rs782575301
NM_000445.5(PLEC):c.919C>T (p.Arg307Cys) rs372997489
NM_000445.5(PLEC):c.9268G>A (p.Gly3090Ser) rs782820081
NM_000445.5(PLEC):c.9304C>T (p.Arg3102Trp) rs376638828
NM_000445.5(PLEC):c.9610G>A (p.Asp3204Asn) rs151050583
NM_000445.5(PLEC):c.9733C>T (p.Arg3245Trp) rs368758264
NM_000445.5(PLEC):c.9904C>T (p.Arg3302Cys) rs782733657
NM_000445.5(PLEC):c.9922G>A (p.Val3308Met) rs202005454

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