ClinVar Miner

List of variants in gene CTSD reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP
NM_001909.5(CTSD):c.*10C>T rs768283127
NM_001909.5(CTSD):c.*11G>A rs377057633
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.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.1116C>T (p.Gly372=) rs557342549
NM_001909.5(CTSD):c.1137C>T (p.Ser379=) rs141981301
NM_001909.5(CTSD):c.1215C>A (p.Gly405=) rs138733377
NM_001909.5(CTSD):c.1230C>T (p.Ala410=) rs772742148
NM_001909.5(CTSD):c.14G>C (p.Ser5Thr) rs764386803
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.189C>T (p.Thr63=) rs114051835
NM_001909.5(CTSD):c.231C>T (p.Ala77=) rs2230067
NM_001909.5(CTSD):c.267C>G (p.Pro89=) rs139154882
NM_001909.5(CTSD):c.352+10G>C rs775828680
NM_001909.5(CTSD):c.393C>T (p.Tyr131=) rs776128996
NM_001909.5(CTSD):c.465T>C (p.Thr155=) rs11555039
NM_001909.5(CTSD):c.472-15T>C rs758874267
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.552G>A (p.Lys184=) rs765849046
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.636G>T (p.Leu212=) rs567625495
NM_001909.5(CTSD):c.68+10C>G rs760082760
NM_001909.5(CTSD):c.68+10C>T rs760082760
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.704+18C>T rs371260793
NM_001909.5(CTSD):c.705-4C>T rs1057521968
NM_001909.5(CTSD):c.780C>T (p.Ser260=) rs1404000220
NM_001909.5(CTSD):c.827+9T>A rs757270638
NM_001909.5(CTSD):c.828-4G>A rs371034011
NM_001909.5(CTSD):c.828-5C>T rs762444592
NM_001909.5(CTSD):c.844G>A (p.Gly282Arg) rs147278302
NM_001909.5(CTSD):c.867C>T (p.Gly289=) rs1200494428
NM_001909.5(CTSD):c.90G>A (p.Thr30=) rs368529527
NM_001909.5(CTSD):c.926G>A (p.Arg309His) rs374540411
NM_001909.5(CTSD):c.945C>T (p.Ile315=) rs752172496
NM_001909.5(CTSD):c.972+10G>A rs531682785
NM_001909.5(CTSD):c.972+7G>A rs371747998

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