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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_001909.5(CTSD):c.465T>C (p.Thr155=)	rs11555039	0.08387
NM_001909.5(CTSD):c.231C>T (p.Ala77=)	rs2230067	0.06127
NM_001909.5(CTSD):c.1215C>A (p.Gly405=)	rs138733377	0.01277
NM_001909.5(CTSD):c.844G>A (p.Gly282Arg)	rs147278302	0.00650
NM_001909.5(CTSD):c.1072-7G>A	rs149019571	0.00560
NM_001909.5(CTSD):c.1071+7G>A	rs374010531	0.00029
NM_001909.5(CTSD):c.68+10C>T	rs760082760	0.00020
NM_001909.5(CTSD):c.*14C>T	rs556410676	0.00013
NM_001909.5(CTSD):c.1230C>T (p.Ala410=)	rs772742148	0.00013
NM_001909.5(CTSD):c.1137C>T (p.Ser379=)	rs141981301	0.00008
NM_001909.5(CTSD):c.627C>T (p.Asn209=)	rs772453588	0.00006
NM_001909.5(CTSD):c.534C>G (p.Val178=)	rs758852382	0.00005
NM_001909.5(CTSD):c.1071+9G>A	rs747408239	0.00004
NM_001909.5(CTSD):c.393C>T (p.Tyr131=)	rs776128996	0.00004
NM_001909.5(CTSD):c.510C>T (p.Gly170=)	rs749196696	0.00004
NM_001909.5(CTSD):c.972+7G>A	rs371747998	0.00004
NM_001909.5(CTSD):c.704+18C>T	rs371260793	0.00003
NM_001909.5(CTSD):c.828-5C>T	rs762444592	0.00003
NM_001909.5(CTSD):c.945C>T (p.Ile315=)	rs752172496	0.00003
NM_001909.5(CTSD):c.*10C>T	rs768283127	0.00002
NM_001909.5(CTSD):c.*11G>A	rs377057633	0.00001
NM_001909.5(CTSD):c.*17G>A	rs201616935	0.00001
NM_001909.5(CTSD):c.472-15T>C	rs758874267	0.00001
NM_001909.5(CTSD):c.492G>A (p.Ser164=)	rs577842448	0.00001
NM_001909.5(CTSD):c.552G>A (p.Lys184=)	rs765849046	0.00001
NM_001909.5(CTSD):c.621C>A (p.Ser207=)	rs367978332	0.00001
NM_001909.5(CTSD):c.636G>T (p.Leu212=)	rs567625495	0.00001
NM_001909.5(CTSD):c.705-4C>T	rs1057521968	0.00001
NM_001909.5(CTSD):c.827+9T>A	rs757270638	0.00001
NM_001909.5(CTSD):c.972+10G>A	rs531682785	0.00001
NM_001909.5(CTSD):c.*15G>A	rs745784791
NM_001909.5(CTSD):c.*4C>G	rs1057521403
NM_001909.5(CTSD):c.1071+12A>T	rs113936232
NM_001909.5(CTSD):c.352+10G>C	rs775828680
NM_001909.5(CTSD):c.497C>T (p.Ala166Val)	rs796052396
NM_001909.5(CTSD):c.68+10C>G	rs760082760
NM_001909.5(CTSD):c.780C>T (p.Ser260=)	rs1404000220
NM_001909.5(CTSD):c.867C>T (p.Gly289=)	rs1200494428

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