ClinVar Miner

List of variants in gene CTSD reported as likely benign

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Gene type:
ClinVar version:
Total variants: 151
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HGVS dbSNP
NC_000011.10:g.1764137C>T rs536065000
NC_000011.10:g.1764217C>T rs191726273
NM_001909.5(CTSD):c.*10C>T rs768283127
NM_001909.5(CTSD):c.*11G>A rs377057633
NM_001909.5(CTSD):c.*140G>T rs551607350
NM_001909.5(CTSD):c.*14C>T rs556410676
NM_001909.5(CTSD):c.*15G>A rs745784791
NM_001909.5(CTSD):c.*17G>A rs201616935
NM_001909.5(CTSD):c.*4C>G rs1057521403
NM_001909.5(CTSD):c.-30G>C rs937590868
NM_001909.5(CTSD):c.-32C>T rs1057523809
NM_001909.5(CTSD):c.-36G>C rs1474705113
NM_001909.5(CTSD):c.-37G>A rs756112449
NM_001909.5(CTSD):c.-40C>T rs780212490
NM_001909.5(CTSD):c.-45A>G rs1167050955
NM_001909.5(CTSD):c.-53C>T rs530324803
NM_001909.5(CTSD):c.-6G>T rs951801692
NM_001909.5(CTSD):c.1008C>T (p.Pro336=)
NM_001909.5(CTSD):c.1009G>A (p.Ala337Thr) rs147800688
NM_001909.5(CTSD):c.100C>T (p.Arg34Trp) rs779278368
NM_001909.5(CTSD):c.1023G>A (p.Lys341=) rs111849172
NM_001909.5(CTSD):c.1047G>A (p.Leu349=)
NM_001909.5(CTSD):c.1062C>T (p.Tyr354=) rs764106396
NM_001909.5(CTSD):c.1065G>A (p.Thr355=)
NM_001909.5(CTSD):c.1071+10C>A
NM_001909.5(CTSD):c.1071+12A>T rs113936232
NM_001909.5(CTSD):c.1071+7G>A rs374010531
NM_001909.5(CTSD):c.1071+9G>A rs747408239
NM_001909.5(CTSD):c.1072-7G>A rs149019571
NM_001909.5(CTSD):c.1077G>A (p.Ser359=) rs138940129
NM_001909.5(CTSD):c.1083C>T (p.Ala361=)
NM_001909.5(CTSD):c.1101G>A (p.Leu367=) rs777289049
NM_001909.5(CTSD):c.1104C>T (p.Ser368=)
NM_001909.5(CTSD):c.1116C>T (p.Gly372=) rs557342549
NM_001909.5(CTSD):c.111G>A (p.Ser37=) rs535140505
NM_001909.5(CTSD):c.1122C>T (p.Asp374=) rs145821780
NM_001909.5(CTSD):c.1128G>A (p.Pro376=) rs929763593
NM_001909.5(CTSD):c.1137C>T (p.Ser379=) rs141981301
NM_001909.5(CTSD):c.1140G>A (p.Gly380=)
NM_001909.5(CTSD):c.1170C>T (p.Ile390=)
NM_001909.5(CTSD):c.1202A>G (p.Asn401Ser) rs147553344
NM_001909.5(CTSD):c.1215C>A (p.Gly405=) rs138733377
NM_001909.5(CTSD):c.1221C>T (p.Ala407=) rs1439111867
NM_001909.5(CTSD):c.1230C>T (p.Ala410=) rs772742148
NM_001909.5(CTSD):c.1236C>G (p.Leu412=) rs1565018392
NM_001909.5(CTSD):c.14G>C (p.Ser5Thr) rs764386803
NM_001909.5(CTSD):c.153C>T (p.Pro51=) rs560041488
NM_001909.5(CTSD):c.154G>A (p.Val52Ile) rs143517230
NM_001909.5(CTSD):c.173C>T (p.Ala58Val) rs17571
NM_001909.5(CTSD):c.174G>A (p.Ala58=) rs565191387
NM_001909.5(CTSD):c.180A>G (p.Pro60=) rs749805002
NM_001909.5(CTSD):c.183C>T (p.Ala61=)
NM_001909.5(CTSD):c.189C>T (p.Thr63=) rs114051835
NM_001909.5(CTSD):c.195G>T (p.Gly65=)
NM_001909.5(CTSD):c.19C>T (p.Leu7=)
NM_001909.5(CTSD):c.204C>T (p.Pro68=)
NM_001909.5(CTSD):c.216G>A (p.Lys72=) rs764982673
NM_001909.5(CTSD):c.229-25C>T rs112184520
NM_001909.5(CTSD):c.231C>T (p.Ala77=) rs2230067
NM_001909.5(CTSD):c.237C>T (p.Tyr79=) rs996421254
NM_001909.5(CTSD):c.240C>T (p.Tyr80=) rs147641822
NM_001909.5(CTSD):c.24G>C (p.Pro8=)
NM_001909.5(CTSD):c.261G>A (p.Thr87=) rs372181453
NM_001909.5(CTSD):c.267C>G (p.Pro89=) rs139154882
NM_001909.5(CTSD):c.288C>T (p.Phe96=) rs778220078
NM_001909.5(CTSD):c.306C>T (p.Asn102=) rs1258957118
NM_001909.5(CTSD):c.345C>T (p.Ile115=) rs200875086
NM_001909.5(CTSD):c.352+10G>C rs775828680
NM_001909.5(CTSD):c.352+42T>C rs149907533
NM_001909.5(CTSD):c.352+48A>G rs139068420
NM_001909.5(CTSD):c.352+8A>T rs944771031
NM_001909.5(CTSD):c.352+9C>T
NM_001909.5(CTSD):c.353-12C>T rs141523461
NM_001909.5(CTSD):c.353-4G>A
NM_001909.5(CTSD):c.353-8C>T rs760934292
NM_001909.5(CTSD):c.353-9C>T
NM_001909.5(CTSD):c.37C>T (p.Leu13=) rs763474887
NM_001909.5(CTSD):c.393C>T (p.Tyr131=) rs776128996
NM_001909.5(CTSD):c.408C>G (p.Thr136=) rs1060504644
NM_001909.5(CTSD):c.410C>T (p.Ser137Leu) rs777645484
NM_001909.5(CTSD):c.444C>T (p.Ser148=)
NM_001909.5(CTSD):c.447G>A (p.Gly149=) rs752032660
NM_001909.5(CTSD):c.465T>C (p.Thr155=) rs11555039
NM_001909.5(CTSD):c.472-11C>G
NM_001909.5(CTSD):c.472-15T>C rs758874267
NM_001909.5(CTSD):c.472-27G>T rs146434428
NM_001909.5(CTSD):c.489G>A (p.Ala163=) rs767476700
NM_001909.5(CTSD):c.492G>A (p.Ser164=) rs577842448
NM_001909.5(CTSD):c.497C>T (p.Ala166Val) rs796052396
NM_001909.5(CTSD):c.510C>T (p.Gly170=) rs749196696
NM_001909.5(CTSD):c.534C>G (p.Val178=) rs758852382
NM_001909.5(CTSD):c.537T>C (p.Phe179=)
NM_001909.5(CTSD):c.54C>T (p.Ala18=)
NM_001909.5(CTSD):c.552G>A (p.Lys184=) rs765849046
NM_001909.5(CTSD):c.570C>T (p.Phe190=) rs1325097000
NM_001909.5(CTSD):c.606C>G (p.Ala202=)
NM_001909.5(CTSD):c.621C>A (p.Ser207=) rs367978332
NM_001909.5(CTSD):c.627C>T (p.Asn209=) rs772453588
NM_001909.5(CTSD):c.630C>T (p.Asn210=) rs375282504
NM_001909.5(CTSD):c.633G>C (p.Val211=) rs1565021103
NM_001909.5(CTSD):c.636G>T (p.Leu212=) rs567625495
NM_001909.5(CTSD):c.639C>G (p.Pro213=) rs146073498
NM_001909.5(CTSD):c.639C>T (p.Pro213=)
NM_001909.5(CTSD):c.63C>T (p.Leu21=) rs1021613206
NM_001909.5(CTSD):c.651C>T (p.Asn217=)
NM_001909.5(CTSD):c.654G>A (p.Leu218=)
NM_001909.5(CTSD):c.675C>T (p.Asp225=)
NM_001909.5(CTSD):c.68+10C>G rs760082760
NM_001909.5(CTSD):c.68+10C>T rs760082760
NM_001909.5(CTSD):c.68+251G>C rs147731370
NM_001909.5(CTSD):c.69-12C>T rs764025297
NM_001909.5(CTSD):c.69-16G>A rs377703110
NM_001909.5(CTSD):c.69-17C>A rs371858126
NM_001909.5(CTSD):c.69-64C>T rs116662058
NM_001909.5(CTSD):c.693C>T (p.Phe231=)
NM_001909.5(CTSD):c.697C>T (p.Leu233=) rs142330967
NM_001909.5(CTSD):c.6G>A (p.Gln2=) rs1328097097
NM_001909.5(CTSD):c.704+18C>T rs371260793
NM_001909.5(CTSD):c.705-4C>T rs1057521968
NM_001909.5(CTSD):c.726G>A (p.Gly242=)
NM_001909.5(CTSD):c.729T>C (p.Gly243=) rs774691757
NM_001909.5(CTSD):c.753C>T (p.Asp251=)
NM_001909.5(CTSD):c.75G>A (p.Pro25=) rs140563067
NM_001909.5(CTSD):c.771T>C (p.Gly257=)
NM_001909.5(CTSD):c.780C>T (p.Ser260=) rs1404000220
NM_001909.5(CTSD):c.816C>A (p.Val272=) rs1554962441
NM_001909.5(CTSD):c.827+13T>C rs369602025
NM_001909.5(CTSD):c.827+9T>A rs757270638
NM_001909.5(CTSD):c.828-19A>C rs200047861
NM_001909.5(CTSD):c.828-247_828-221del rs1219998189
NM_001909.5(CTSD):c.828-4G>A rs371034011
NM_001909.5(CTSD):c.828-5C>T rs762444592
NM_001909.5(CTSD):c.843C>T (p.Ser281=)
NM_001909.5(CTSD):c.844G>A (p.Gly282Arg) rs147278302
NM_001909.5(CTSD):c.849G>A (p.Leu283=)
NM_001909.5(CTSD):c.867C>T (p.Gly289=) rs1200494428
NM_001909.5(CTSD):c.882G>A (p.Val294=) rs778999077
NM_001909.5(CTSD):c.90G>A (p.Thr30=) rs368529527
NM_001909.5(CTSD):c.912G>A (p.Pro304=) rs140238987
NM_001909.5(CTSD):c.918T>C (p.Asp306=)
NM_001909.5(CTSD):c.926G>A (p.Arg309His) rs374540411
NM_001909.5(CTSD):c.933G>A (p.Leu311=) rs1428157464
NM_001909.5(CTSD):c.945C>T (p.Ile315=) rs752172496
NM_001909.5(CTSD):c.957G>A (p.Pro319=) rs369229897
NM_001909.5(CTSD):c.972+10G>A rs531682785
NM_001909.5(CTSD):c.972+7G>A rs371747998
NM_001909.5(CTSD):c.972+9C>T rs746243061
NM_001909.5(CTSD):c.973-10C>T
NM_001909.5(CTSD):c.973-14G>A rs1354741089
NM_001909.5(CTSD):c.993G>A (p.Lys331=) rs1181418072
NM_001909.5(CTSD):c.99C>G (p.Arg33=) rs1590908750

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