List of variants in gene SPART reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_015087.5(SPART):c.1130A>T (p.Lys377Met)	rs148672324	0.00191
NM_015087.5(SPART):c.1172A>G (p.Asp391Gly)	rs148833652	0.00123
NM_015087.5(SPART):c.68C>A (p.Ala23Asp)	rs753340463	0.00001
NM_015087.5(SPART):c.1147G>A (p.Gly383Arg)
NM_015087.5(SPART):c.265C>T (p.Arg89Cys)	rs369491741
NM_015087.5(SPART):c.719G>T (p.Ser240Ile)	rs1566131408

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