List of variants in gene CTSD reported as 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: 31

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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.353-17C>T	rs7126177	0.06731
NM_001909.5(CTSD):c.231C>T (p.Ala77=)	rs2230067	0.06127
NM_001909.5(CTSD):c.828-17G>A	rs78735768	0.05315
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.846G>A (p.Gly282=)	rs112021026	0.00567
NM_001909.5(CTSD):c.1072-7G>A	rs149019571	0.00560
NM_001909.5(CTSD):c.828-19A>C	rs200047861	0.00494
NM_001909.5(CTSD):c.*19G>A	rs201434721	0.00493
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.951C>T (p.Ala317=)	rs78306946	0.00211
NM_001909.5(CTSD):c.639C>G (p.Pro213=)	rs146073498	0.00197
NM_001909.5(CTSD):c.353-11G>A	rs372689713	0.00039
NM_001909.5(CTSD):c.827+13T>C	rs369602025	0.00036
NM_001909.5(CTSD):c.1071+12A>G	rs113936232	0.00034
NM_001909.5(CTSD):c.1071+7G>A	rs374010531	0.00029
NM_001909.5(CTSD):c.828-18C>T	rs377228580	0.00022
NM_001909.5(CTSD):c.240C>T (p.Tyr80=)	rs147641822	0.00019
NM_001909.5(CTSD):c.294G>A (p.Thr98=)	rs369373285	0.00019
NM_001909.5(CTSD):c.1077G>A (p.Ser359=)	rs138940129	0.00013
NM_001909.5(CTSD):c.957G>A (p.Pro319=)	rs369229897	0.00013
NM_001909.5(CTSD):c.1122C>T (p.Asp374=)	rs145821780	0.00011
NM_001909.5(CTSD):c.471+15G>C	rs201413619	0.00008
NM_001909.5(CTSD):c.630C>T (p.Asn210=)	rs375282504	0.00008
NM_001909.5(CTSD):c.261G>A (p.Thr87=)	rs372181453	0.00007
NM_001909.5(CTSD):c.704+6C>T	rs370847523	0.00004
NM_001909.5(CTSD):c.432G>A (p.Ser144=)	rs587780916	0.00003
NM_001909.5(CTSD):c.270G>A (p.Gln90=)	rs587780915	0.00002
NM_001909.5(CTSD):c.828-14_828-13del	rs796052395	0.00001

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