ClinVar Miner

List of variants in gene TPP1 reported as uncertain significance

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Total variants: 156
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HGVS dbSNP
NM_000391.3(TPP1):c.-33C>G rs757508432
NM_000391.3(TPP1):c.-40T>C rs200184958
NM_000391.4(TPP1):c.*1000T>C rs886048538
NM_000391.4(TPP1):c.*1216dup rs575737269
NM_000391.4(TPP1):c.*1302A>T rs886048537
NM_000391.4(TPP1):c.*1311C>T rs886048536
NM_000391.4(TPP1):c.*1412T>G rs886048535
NM_000391.4(TPP1):c.*1428T>C rs188544089
NM_000391.4(TPP1):c.*1570C>T rs369352772
NM_000391.4(TPP1):c.*1634T>C rs886048534
NM_000391.4(TPP1):c.*1715T>C rs886048533
NM_000391.4(TPP1):c.*1774G>A rs886048532
NM_000391.4(TPP1):c.*312T>C rs201122774
NM_000391.4(TPP1):c.*314del rs202155605
NM_000391.4(TPP1):c.*44T>A rs370517226
NM_000391.4(TPP1):c.*668C>A rs886048539
NM_000391.4(TPP1):c.*785T>G rs764323122
NM_000391.4(TPP1):c.*986C>G rs188148381
NM_000391.4(TPP1):c.-21G>A rs760667554
NM_000391.4(TPP1):c.1009A>C (p.Ile337Leu)
NM_000391.4(TPP1):c.1016G>A (p.Arg339Gln) rs765380155
NM_000391.4(TPP1):c.101G>A (p.Gly34Asp) rs138448968
NM_000391.4(TPP1):c.1033A>C (p.Met345Leu) rs141482368
NM_000391.4(TPP1):c.1042_1047del (p.Ala348_Ala349del) rs1554901785
NM_000391.4(TPP1):c.1045G>A (p.Ala349Thr) rs1085307673
NM_000391.4(TPP1):c.1048C>T (p.Arg350Trp) rs1554901784
NM_000391.4(TPP1):c.1049G>A (p.Arg350Gln) rs199866669
NM_000391.4(TPP1):c.1058C>A (p.Thr353Asn) rs145966505
NM_000391.4(TPP1):c.1069G>A (p.Ala357Thr) rs1266615275
NM_000391.4(TPP1):c.1080C>A (p.Asp360Glu) rs1564854760
NM_000391.4(TPP1):c.1116C>G (p.His372Gln) rs751321300
NM_000391.4(TPP1):c.1116C>T (p.His372=) rs751321300
NM_000391.4(TPP1):c.1123C>T (p.Arg375Cys)
NM_000391.4(TPP1):c.1134C>G (p.Phe378Leu) rs1554901719
NM_000391.4(TPP1):c.1138G>A (p.Ala380Thr) rs190013230
NM_000391.4(TPP1):c.1145G>C (p.Ser382Thr)
NM_000391.4(TPP1):c.1181A>G (p.Gln394Arg) rs796053442
NM_000391.4(TPP1):c.118C>T (p.Arg40Cys) rs794727482
NM_000391.4(TPP1):c.1192C>T (p.Leu398Phe) rs149319579
NM_000391.4(TPP1):c.119G>A (p.Arg40His)
NM_000391.4(TPP1):c.1205A>G (p.Glu402Gly) rs1471156821
NM_000391.4(TPP1):c.1208T>C (p.Ile403Thr) rs1564854446
NM_000391.4(TPP1):c.1217A>G (p.Tyr406Cys) rs780670020
NM_000391.4(TPP1):c.123G>A (p.Ala41=) rs747260298
NM_000391.4(TPP1):c.1241A>T (p.Asn414Ile) rs146798796
NM_000391.4(TPP1):c.1252C>T (p.Arg418Trp)
NM_000391.4(TPP1):c.127C>G (p.Pro43Ala) rs1314595290
NM_000391.4(TPP1):c.1280C>T (p.Thr427Met) rs201034755
NM_000391.4(TPP1):c.1281G>A (p.Thr427=) rs577520250
NM_000391.4(TPP1):c.1289T>A (p.Leu430Gln) rs780656523
NM_000391.4(TPP1):c.128C>G (p.Pro43Arg) rs796053434
NM_000391.4(TPP1):c.1300C>T (p.Pro434Ser) rs1420637772
NM_000391.4(TPP1):c.1303C>G (p.His435Asp) rs755829911
NM_000391.4(TPP1):c.1307T>C (p.Leu436Pro) rs150039898
NM_000391.4(TPP1):c.1328A>G (p.Asn443Ser) rs139343938
NM_000391.4(TPP1):c.1331C>A (p.Ala444Asp) rs760974302
NM_000391.4(TPP1):c.1339C>T (p.Arg447Cys) rs1035033641
NM_000391.4(TPP1):c.1351G>T (p.Asp451Tyr)
NM_000391.4(TPP1):c.138G>T (p.Glu46Asp) rs778900807
NM_000391.4(TPP1):c.1402A>C (p.Ile468Leu) rs796053443
NM_000391.4(TPP1):c.1435C>G (p.Pro479Ala) rs756530648
NM_000391.4(TPP1):c.1451T>C (p.Ile484Thr) rs748533410
NM_000391.4(TPP1):c.1466A>G (p.Asn489Ser) rs751645191
NM_000391.4(TPP1):c.1489C>T (p.Arg497Cys) rs377700188
NM_000391.4(TPP1):c.1490G>A (p.Arg497His) rs549928656
NM_000391.4(TPP1):c.1494C>T (p.Pro498=) rs117942457
NM_000391.4(TPP1):c.1495C>G (p.Pro499Ala) rs201126448
NM_000391.4(TPP1):c.1496C>G (p.Pro499Arg) rs773707856
NM_000391.4(TPP1):c.1496C>T (p.Pro499Leu) rs773707856
NM_000391.4(TPP1):c.14C>A (p.Ala5Asp) rs138976576
NM_000391.4(TPP1):c.1526A>G (p.Gln509Arg) rs149529997
NM_000391.4(TPP1):c.1543C>T (p.Leu515Phe) rs748345018
NM_000391.4(TPP1):c.1547_1548del (p.Leu515_Phe516insTer) rs763961289
NM_000391.4(TPP1):c.1551+5G>A rs778756815
NM_000391.4(TPP1):c.1552-4del
NM_000391.4(TPP1):c.1552-9C>T rs369699167
NM_000391.4(TPP1):c.1558C>A (p.Arg520Ser) rs371204585
NM_000391.4(TPP1):c.1558C>T (p.Arg520Cys)
NM_000391.4(TPP1):c.1559G>A (p.Arg520His)
NM_000391.4(TPP1):c.1610G>A (p.Cys537Tyr) rs777744177
NM_000391.4(TPP1):c.1613C>G (p.Ser538Cys)
NM_000391.4(TPP1):c.163C>G (p.Gln55Glu)
NM_000391.4(TPP1):c.1642T>C (p.Trp548Arg) rs1348967263
NM_000391.4(TPP1):c.1653C>G (p.Pro551=) rs372564255
NM_000391.4(TPP1):c.1664C>A (p.Ala555Asp) rs200880556
NM_000391.4(TPP1):c.17G>C (p.Cys6Ser)
NM_000391.4(TPP1):c.197A>T (p.Gln66Leu) rs751088292
NM_000391.4(TPP1):c.200C>G (p.Ala67Gly) rs796053435
NM_000391.4(TPP1):c.202G>A (p.Val68Met)
NM_000391.4(TPP1):c.206C>G (p.Ser69Trp) rs769028551
NM_000391.4(TPP1):c.209A>G (p.Asp70Gly)
NM_000391.4(TPP1):c.225A>G (p.Gln75=) rs368709098
NM_000391.4(TPP1):c.244C>T (p.Leu82=) rs794727623
NM_000391.4(TPP1):c.260A>G (p.Asp87Gly) rs148064565
NM_000391.4(TPP1):c.284C>G (p.Thr95Ser)
NM_000391.4(TPP1):c.293C>T (p.Thr98Met) rs140726254
NM_000391.4(TPP1):c.295G>C (p.Val99Leu)
NM_000391.4(TPP1):c.319G>A (p.Gly107Arg) rs201613668
NM_000391.4(TPP1):c.37C>T (p.Leu13Phe) rs796053445
NM_000391.4(TPP1):c.404G>A (p.Gly135Glu) rs796053436
NM_000391.4(TPP1):c.425T>G (p.Val142Gly) rs775217501
NM_000391.4(TPP1):c.437C>T (p.Thr146Met)
NM_000391.4(TPP1):c.457T>C (p.Ser153Pro) rs1554902028
NM_000391.4(TPP1):c.473A>C (p.Gln158Pro) rs757507462
NM_000391.4(TPP1):c.497A>T (p.His166Leu) rs796053437
NM_000391.4(TPP1):c.508+2dup rs1554902017
NM_000391.4(TPP1):c.510G>A (p.Val170=) rs751488322
NM_000391.4(TPP1):c.511G>C (p.Gly171Arg) rs994636765
NM_000391.4(TPP1):c.520C>T (p.His174Tyr) rs796053438
NM_000391.4(TPP1):c.523C>T (p.Arg175Cys) rs750241218
NM_000391.4(TPP1):c.524G>A (p.Arg175His) rs764922748
NM_000391.4(TPP1):c.532C>G (p.Pro178Ala) rs149986601
NM_000391.4(TPP1):c.542C>T (p.Ser181Phe) rs139059149
NM_000391.4(TPP1):c.554G>A (p.Arg185His) rs773455971
NM_000391.4(TPP1):c.572C>T (p.Thr191Ile)
NM_000391.4(TPP1):c.580G>A (p.Val194Ile) rs1303710593
NM_000391.4(TPP1):c.626A>G (p.Tyr209Cys) rs1554901957
NM_000391.4(TPP1):c.638C>T (p.Ser213Leu) rs773546205
NM_000391.4(TPP1):c.65G>A (p.Ser22Asn) rs202025584
NM_000391.4(TPP1):c.665A>C (p.Asn222Thr)
NM_000391.4(TPP1):c.665A>G (p.Asn222Ser) rs372787642
NM_000391.4(TPP1):c.687+20C>T rs569432039
NM_000391.4(TPP1):c.687+6C>T rs768924191
NM_000391.4(TPP1):c.694G>A (p.Glu232Lys)
NM_000391.4(TPP1):c.6A>T (p.Gly2=) rs747594496
NM_000391.4(TPP1):c.731T>C (p.Met244Thr) rs1554901895
NM_000391.4(TPP1):c.733C>T (p.Arg245Cys) rs587780481
NM_000391.4(TPP1):c.734G>A (p.Arg245His)
NM_000391.4(TPP1):c.746G>T (p.Gly249Val)
NM_000391.4(TPP1):c.772G>T (p.Ala258Ser)
NM_000391.4(TPP1):c.775C>T (p.Arg259Cys)
NM_000391.4(TPP1):c.776G>A (p.Arg259His) rs140176031
NM_000391.4(TPP1):c.782T>C (p.Val261Ala)
NM_000391.4(TPP1):c.78C>A (p.Asp26Glu) rs760252179
NM_000391.4(TPP1):c.796C>T (p.Arg266Trp) rs200138397
NM_000391.4(TPP1):c.797G>A (p.Arg266Gln) rs757953998
NM_000391.4(TPP1):c.7C>A (p.Leu3Ile) rs142163063
NM_000391.4(TPP1):c.808G>A (p.Gly270Arg) rs561854371
NM_000391.4(TPP1):c.812T>C (p.Ile271Thr)
NM_000391.4(TPP1):c.833A>C (p.Gln278Pro) rs796053439
NM_000391.4(TPP1):c.83G>A (p.Arg28Gln) rs369126677
NM_000391.4(TPP1):c.840G>C (p.Leu280=) rs140349036
NM_000391.4(TPP1):c.858C>A (p.Asn286Lys) rs1420315178
NM_000391.4(TPP1):c.866C>A (p.Thr289Asn) rs1426277822
NM_000391.4(TPP1):c.886+7C>T rs886048543
NM_000391.4(TPP1):c.887-10A>G rs755445790
NM_000391.4(TPP1):c.887-18A>G rs935526225
NM_000391.4(TPP1):c.887-5del rs886048540
NM_000391.4(TPP1):c.887-6_887-5del rs886048541
NM_000391.4(TPP1):c.887-6del rs35039601
NM_000391.4(TPP1):c.890G>A (p.Arg297Gln) rs796053441
NM_000391.4(TPP1):c.89C>A (p.Thr30Lys)
NM_000391.4(TPP1):c.947C>A (p.Ala316Asp) rs149463616
NM_000391.4(TPP1):c.956A>G (p.His319Arg)
NM_000391.4(TPP1):c.959T>G (p.Val320Gly) rs1314521780
NM_000391.4(TPP1):c.992C>T (p.Ser331Phe) rs755386210

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