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

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_001909.5(CTSD):c.352+42T>C	rs149907533	0.01641
NM_001909.5(CTSD):c.704+183G>A	rs115786275	0.01477
NM_001909.5(CTSD):c.1215C>A (p.Gly405=)	rs138733377	0.01277
NM_001909.5(CTSD):c.352+48A>G	rs139068420	0.01106
NM_001909.5(CTSD):c.472-27G>T	rs146434428	0.00795
NM_001909.5(CTSD):c.844G>A (p.Gly282Arg)	rs147278302	0.00650
NM_001909.5(CTSD):c.229-25C>T	rs112184520	0.00603
NM_001909.5(CTSD):c.1072-7G>A	rs149019571	0.00560
NM_001909.5(CTSD):c.827+73C>T	rs201119619	0.00542
NM_001909.5(CTSD):c.*288G>A	rs112529968	0.00541
NM_001909.5(CTSD):c.828-19A>C	rs200047861	0.00494
NM_001909.5(CTSD):c.353-12C>T	rs141523461	0.00468
NM_001909.5(CTSD):c.912G>A (p.Pro304=)	rs140238987	0.00281
NM_001909.5(CTSD):c.827+22C>T	rs113641298	0.00253
NM_001909.5(CTSD):c.639C>G (p.Pro213=)	rs146073498	0.00197
NM_001909.5(CTSD):c.1071+12A>G	rs113936232	0.00034
NM_001909.5(CTSD):c.1077G>A (p.Ser359=)	rs138940129	0.00013
NM_001909.5(CTSD):c.1137C>T (p.Ser379=)	rs141981301	0.00008
NM_001909.5(CTSD):c.267C>G (p.Pro89=)	rs139154882	0.00006
NM_001909.5(CTSD):c.926G>A (p.Arg309His)	rs374540411	0.00006
NM_001909.5(CTSD):c.447G>A (p.Gly149=)	rs752032660	0.00004
NM_001909.5(CTSD):c.828-4G>A	rs371034011	0.00004
NM_001909.5(CTSD):c.1116C>T (p.Gly372=)	rs557342549	0.00001
NM_001909.5(CTSD):c.1158C>T (p.Gly386=)	rs762076054	0.00001
NM_001909.5(CTSD):c.366G>A (p.Lys122=)	rs369424685	0.00001
NM_001909.5(CTSD):c.489G>A (p.Ala163=)	rs767476700	0.00001
NM_001909.5(CTSD):c.558A>G (p.Pro186=)	rs755670512	0.00001
NM_001909.5(CTSD):c.973-14G>A	rs1354741089	0.00001
NM_001909.5(CTSD):c.*207TC[2]	rs199970387
NM_001909.5(CTSD):c.1023G>A (p.Lys341=)	rs111849172
NM_001909.5(CTSD):c.1072-41G>C	rs138305981
NM_001909.5(CTSD):c.705-21A>T	rs2292964
NM_001909.5(CTSD):c.828-247_828-221del	rs1219998189

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