ClinVar Miner

List of variants in gene TPP1 reported as likely benign

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Total variants: 90
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HGVS dbSNP
NC_000011.10:g.6619449A>G
NM_000391.3(TPP1):c.-33C>G rs757508432
NM_000391.3(TPP1):c.-33C>T rs757508432
NM_000391.3(TPP1):c.887-10_887-6delAAAAA rs35039601
NM_000391.4(TPP1):c.*71G>A rs140680586
NM_000391.4(TPP1):c.-12C>T rs770733577
NM_000391.4(TPP1):c.-20C>G rs368143492
NM_000391.4(TPP1):c.-22A>C rs767860643
NM_000391.4(TPP1):c.-3A>G rs762785189
NM_000391.4(TPP1):c.1033A>C (p.Met345Leu) rs141482368
NM_000391.4(TPP1):c.1044C>T (p.Ala348=) rs35706972
NM_000391.4(TPP1):c.1076-17C>T
NM_000391.4(TPP1):c.1076-18A>G rs78676565
NM_000391.4(TPP1):c.1076-7C>T rs746276384
NM_000391.4(TPP1):c.1086G>A (p.Gly362=) rs140809393
NM_000391.4(TPP1):c.1089C>T (p.Ala363=) rs151068181
NM_000391.4(TPP1):c.1125C>T (p.Arg375=) rs587780972
NM_000391.4(TPP1):c.1146-18G>A rs72909098
NM_000391.4(TPP1):c.122C>T (p.Ala41Val)
NM_000391.4(TPP1):c.123G>A (p.Ala41=) rs747260298
NM_000391.4(TPP1):c.1253G>A (p.Arg418Gln) rs138744051
NM_000391.4(TPP1):c.1266+5G>A rs1800753
NM_000391.4(TPP1):c.1266+8T>C rs752269166
NM_000391.4(TPP1):c.1267-56_1267-37del rs1554901606
NM_000391.4(TPP1):c.1362A>G (p.Ala454=) rs141701073
NM_000391.4(TPP1):c.1377C>T (p.Tyr459=) rs1554901573
NM_000391.4(TPP1):c.1393A>G (p.Arg465Gly) rs796053433
NM_000391.4(TPP1):c.139C>T (p.Leu47=) rs1057523084
NM_000391.4(TPP1):c.1407A>T (p.Pro469=) rs750546113
NM_000391.4(TPP1):c.1426-10A>G rs200965587
NM_000391.4(TPP1):c.1426-10A>T rs200965587
NM_000391.4(TPP1):c.1470G>A (p.Glu490=) rs367681647
NM_000391.4(TPP1):c.1494C>T (p.Pro498=) rs117942457
NM_000391.4(TPP1):c.1497T>C (p.Pro499=) rs142672910
NM_000391.4(TPP1):c.14C>A (p.Ala5Asp) rs138976576
NM_000391.4(TPP1):c.1512C>T (p.Asn504=) rs1564854136
NM_000391.4(TPP1):c.1515A>G (p.Pro505=) rs1057521257
NM_000391.4(TPP1):c.1542A>T (p.Gly514=) rs1128396
NM_000391.4(TPP1):c.1551+70C>T
NM_000391.4(TPP1):c.1552-9C>T rs369699167
NM_000391.4(TPP1):c.1569T>C (p.His523=) rs1029334403
NM_000391.4(TPP1):c.1593A>G (p.Val531=) rs1554901473
NM_000391.4(TPP1):c.1653C>G (p.Pro551=) rs372564255
NM_000391.4(TPP1):c.17+17G>A
NM_000391.4(TPP1):c.18-10G>T rs778206032
NM_000391.4(TPP1):c.207G>A (p.Ser69=) rs761070664
NM_000391.4(TPP1):c.213C>T (p.Pro71=) rs143730817
NM_000391.4(TPP1):c.216C>A (p.Ser72Arg) rs796053431
NM_000391.4(TPP1):c.219T>C (p.Ser73=) rs1456089848
NM_000391.4(TPP1):c.229+8T>C rs1263525920
NM_000391.4(TPP1):c.230-19C>T rs1057523929
NM_000391.4(TPP1):c.260A>G (p.Asp87Gly) rs148064565
NM_000391.4(TPP1):c.293C>T (p.Thr98Met) rs140726254
NM_000391.4(TPP1):c.297G>A (p.Val99=) rs753066277
NM_000391.4(TPP1):c.299A>G (p.Gln100Arg) rs1800746
NM_000391.4(TPP1):c.318C>T (p.Ala106=) rs774528021
NM_000391.4(TPP1):c.330G>A (p.Lys110=) rs145853102
NM_000391.4(TPP1):c.380+3G>A rs781744173
NM_000391.4(TPP1):c.381-10dup rs146315473
NM_000391.4(TPP1):c.381-23G>T
NM_000391.4(TPP1):c.381-4C>G rs529421892
NM_000391.4(TPP1):c.420C>T (p.His140=) rs1057521538
NM_000391.4(TPP1):c.441A>G (p.Glu147=) rs2555170
NM_000391.4(TPP1):c.465T>C (p.His155=)
NM_000391.4(TPP1):c.509-5T>C rs375548657
NM_000391.4(TPP1):c.513G>T (p.Gly171=) rs145224171
NM_000391.4(TPP1):c.542C>T (p.Ser181Phe) rs139059149
NM_000391.4(TPP1):c.544C>T (p.Leu182=) rs776858324
NM_000391.4(TPP1):c.553C>T (p.Arg185Cys) rs34758634
NM_000391.4(TPP1):c.645C>T (p.Asp215=) rs766845531
NM_000391.4(TPP1):c.65G>A (p.Ser22Asn) rs202025584
NM_000391.4(TPP1):c.669C>T (p.Asn223=) rs1554901936
NM_000391.4(TPP1):c.687+20C>T rs569432039
NM_000391.4(TPP1):c.688-18C>G
NM_000391.4(TPP1):c.688-18C>T rs376868997
NM_000391.4(TPP1):c.688-43C>T
NM_000391.4(TPP1):c.688-4A>G rs370683758
NM_000391.4(TPP1):c.688-7T>A rs375262484
NM_000391.4(TPP1):c.69G>A (p.Pro23=) rs141680923
NM_000391.4(TPP1):c.6A>T (p.Gly2=) rs747594496
NM_000391.4(TPP1):c.741C>T (p.Phe247=) rs372817942
NM_000391.4(TPP1):c.75C>T (p.Pro25=) rs902447645
NM_000391.4(TPP1):c.796C>T (p.Arg266Trp) rs200138397
NM_000391.4(TPP1):c.816G>A (p.Glu272=) rs1564855114
NM_000391.4(TPP1):c.828T>C (p.Asp276=) rs1057522366
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.90-12C>A
NM_000391.4(TPP1):c.90-44C>T
NM_000391.4(TPP1):c.960G>C (p.Val320=) rs1554901808

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