List of variants in gene TSPEAR 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_144991.3(TSPEAR):c.1224C>G (p.His408Gln)	rs35028190	0.04880
NM_144991.3(TSPEAR):c.552T>C (p.Asp184=)	rs112735071	0.00938
NM_144991.3(TSPEAR):c.534G>A (p.Pro178=)	rs148713881	0.00888
NM_144991.3(TSPEAR):c.51C>T (p.Gly17=)	rs75351275	0.00793
NM_144991.3(TSPEAR):c.1779G>A (p.Ser593=)	rs138358770	0.00468
NM_144991.3(TSPEAR):c.702C>T (p.Asn234=)	rs117791519	0.00468
NM_144991.3(TSPEAR):c.1915G>A (p.Asp639Asn)	rs138480801	0.00244
NM_144991.3(TSPEAR):c.170G>A (p.Arg57Gln)	rs151001222	0.00210
NM_144991.3(TSPEAR):c.343G>A (p.Asp115Asn)	rs144586270	0.00189
NM_144991.3(TSPEAR):c.304-12C>T	rs192955018	0.00180
NM_144991.3(TSPEAR):c.44C>T (p.Ala15Val)	rs150107590	0.00180
NM_144991.3(TSPEAR):c.900C>T (p.Asn300=)	rs139106120	0.00154
NM_144991.3(TSPEAR):c.542+14C>T	rs200116408	0.00148
NM_144991.3(TSPEAR):c.1566+12C>T	rs199557392	0.00128
NM_144991.3(TSPEAR):c.714G>A (p.Ala238=)	rs146025689	0.00090
NM_144991.3(TSPEAR):c.1836G>T (p.Ser612=)	rs112006551

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