ClinVar Miner

List of variants in gene TPP1 reported as uncertain significance for not provided

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Total variants: 62
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HGVS dbSNP
NM_000391.3(TPP1):c.1016G>A (p.Arg339Gln) rs765380155
NM_000391.3(TPP1):c.101G>A (p.Gly34Asp) rs138448968
NM_000391.3(TPP1):c.1045G>A (p.Ala349Thr) rs1085307673
NM_000391.3(TPP1):c.1049G>A (p.Arg350Gln) rs199866669
NM_000391.3(TPP1):c.1069G>A (p.Ala357Thr) rs1266615275
NM_000391.3(TPP1):c.1116C>G (p.His372Gln) rs751321300
NM_000391.3(TPP1):c.1138G>A (p.Ala380Thr) rs190013230
NM_000391.3(TPP1):c.1181A>G (p.Gln394Arg) rs796053442
NM_000391.3(TPP1):c.118C>T (p.Arg40Cys) rs794727482
NM_000391.3(TPP1):c.1217A>G (p.Tyr406Cys) rs780670020
NM_000391.3(TPP1):c.1241A>T (p.Asn414Ile) rs146798796
NM_000391.3(TPP1):c.1252C>T (p.Arg418Trp)
NM_000391.3(TPP1):c.1280C>T (p.Thr427Met) rs201034755
NM_000391.3(TPP1):c.1289T>A (p.Leu430Gln) rs780656523
NM_000391.3(TPP1):c.128C>G (p.Pro43Arg) rs796053434
NM_000391.3(TPP1):c.1303C>G (p.His435Asp) rs755829911
NM_000391.3(TPP1):c.1331C>A (p.Ala444Asp) rs760974302
NM_000391.3(TPP1):c.1339C>T (p.Arg447Cys) rs1035033641
NM_000391.3(TPP1):c.138G>T (p.Glu46Asp) rs778900807
NM_000391.3(TPP1):c.1402A>C (p.Ile468Leu) rs796053443
NM_000391.3(TPP1):c.1490G>A (p.Arg497His) rs549928656
NM_000391.3(TPP1):c.1495C>G (p.Pro499Ala) rs201126448
NM_000391.3(TPP1):c.14C>A (p.Ala5Asp) rs138976576
NM_000391.3(TPP1):c.1526A>G (p.Gln509Arg) rs149529997
NM_000391.3(TPP1):c.1543C>T (p.Leu515Phe) rs748345018
NM_000391.3(TPP1):c.1551+5G>A rs778756815
NM_000391.3(TPP1):c.1552-9C>T rs369699167
NM_000391.3(TPP1):c.1558C>A (p.Arg520Ser) rs371204585
NM_000391.3(TPP1):c.1610G>A (p.Cys537Tyr) rs777744177
NM_000391.3(TPP1):c.1653C>G (p.Pro551=) rs372564255
NM_000391.3(TPP1):c.1664C>A (p.Ala555Asp) rs200880556
NM_000391.3(TPP1):c.197A>T (p.Gln66Leu) rs751088292
NM_000391.3(TPP1):c.200C>G (p.Ala67Gly) rs796053435
NM_000391.3(TPP1):c.206C>G (p.Ser69Trp) rs769028551
NM_000391.3(TPP1):c.244C>T (p.Leu82=) rs794727623
NM_000391.3(TPP1):c.260A>G (p.Asp87Gly) rs148064565
NM_000391.3(TPP1):c.293C>T (p.Thr98Met) rs140726254
NM_000391.3(TPP1):c.319G>A (p.Gly107Arg) rs201613668
NM_000391.3(TPP1):c.37C>T (p.Leu13Phe) rs796053445
NM_000391.3(TPP1):c.404G>A (p.Gly135Glu) rs796053436
NM_000391.3(TPP1):c.425T>G (p.Val142Gly) rs775217501
NM_000391.3(TPP1):c.473A>C (p.Gln158Pro) rs757507462
NM_000391.3(TPP1):c.510G>A (p.Val170=) rs751488322
NM_000391.3(TPP1):c.511G>C (p.Gly171Arg) rs994636765
NM_000391.3(TPP1):c.520C>T (p.His174Tyr) rs796053438
NM_000391.3(TPP1):c.523C>T (p.Arg175Cys) rs750241218
NM_000391.3(TPP1):c.532C>G (p.Pro178Ala) rs149986601
NM_000391.3(TPP1):c.542C>T (p.Ser181Phe) rs139059149
NM_000391.3(TPP1):c.638C>T (p.Ser213Leu) rs773546205
NM_000391.3(TPP1):c.665A>G (p.Asn222Ser) rs372787642
NM_000391.3(TPP1):c.687+20C>T rs569432039
NM_000391.3(TPP1):c.6A>T (p.Gly2=) rs747594496
NM_000391.3(TPP1):c.733C>T (p.Arg245Cys) rs587780481
NM_000391.3(TPP1):c.776G>A (p.Arg259His) rs140176031
NM_000391.3(TPP1):c.796C>T (p.Arg266Trp) rs200138397
NM_000391.3(TPP1):c.797G>A (p.Arg266Gln) rs757953998
NM_000391.3(TPP1):c.7C>A (p.Leu3Ile) rs142163063
NM_000391.3(TPP1):c.887-10A>G rs755445790
NM_000391.3(TPP1):c.887-18A>G rs935526225
NM_000391.3(TPP1):c.890G>A (p.Arg297Gln) rs796053441
NM_000391.3(TPP1):c.947C>A (p.Ala316Asp) rs149463616
NM_000391.3(TPP1):c.992C>T (p.Ser331Phe) rs755386210

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