ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 35
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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.-6G>T rs951801692
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.1062C>T (p.Tyr354=) rs764106396
NM_001909.5(CTSD):c.1072-7G>A rs149019571
NM_001909.5(CTSD):c.1077G>A (p.Ser359=) rs138940129
NM_001909.5(CTSD):c.111G>A (p.Ser37=) rs535140505
NM_001909.5(CTSD):c.1215C>A (p.Gly405=) rs138733377
NM_001909.5(CTSD):c.153C>T (p.Pro51=) rs560041488
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.229-25C>T rs112184520
NM_001909.5(CTSD):c.237C>T (p.Tyr79=) rs996421254
NM_001909.5(CTSD):c.288C>T (p.Phe96=) rs778220078
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.353-12C>T rs141523461
NM_001909.5(CTSD):c.472-27G>T rs146434428
NM_001909.5(CTSD):c.492G>A (p.Ser164=) rs577842448
NM_001909.5(CTSD):c.570C>T (p.Phe190=) rs1325097000
NM_001909.5(CTSD):c.639C>G (p.Pro213=) rs146073498
NM_001909.5(CTSD):c.63C>T (p.Leu21=) rs1021613206
NM_001909.5(CTSD):c.68+251G>C rs147731370
NM_001909.5(CTSD):c.69-64C>T rs116662058
NM_001909.5(CTSD):c.697C>T (p.Leu233=) rs142330967
NM_001909.5(CTSD):c.729T>C (p.Gly243=) rs774691757
NM_001909.5(CTSD):c.828-19A>C rs200047861
NM_001909.5(CTSD):c.828-247_828-221del rs1219998189
NM_001909.5(CTSD):c.844G>A (p.Gly282Arg) rs147278302
NM_001909.5(CTSD):c.973-14G>A rs1354741089
NM_001909.5(CTSD):c.99C>G (p.Arg33=) rs1590908750

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