"PreventionGenetics, part of Exact Sciences"[submitter] AND "SPARC"[ge - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3031376	NM_003118.4(SPARC):c.*47C>T	LOC126807556, SPARC	Single nucleotide variant (3 prime UTR variant +1 more)	SPARC-related disorder	GLikely benign
Select item 3054232	NM_003118.4(SPARC):c.873C>T (p.Gly291=)	LOC126807556, SPARC	Single nucleotide variant (synonymous variant)	SPARC-related disorder	GLikely benign
Select item 733348	NM_003118.4(SPARC):c.861C>T (p.Ala287=)	LOC126807556, SPARC	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 747118	NM_003118.4(SPARC):c.816C>A (p.Thr272=)	LOC126807556, SPARC	Single nucleotide variant (synonymous variant)	SPARC-related disorder +1 more	GLikely benign
Select item 1594661	NM_003118.4(SPARC):c.771T>C (p.Ala257=)	LOC126807556, SPARC	Single nucleotide variant (synonymous variant)	SPARC-related disorder +1 more	GLikely benign
Select item 785151	NM_003118.4(SPARC):c.733G>A (p.Gly245Arg)	SPARC (G244R +1 more)	Single nucleotide variant (missense variant)	Osteogenesis imperfecta +3 more	GConflicting classifications of pathogenicity
Select item 733646	NM_003118.4(SPARC):c.633C>T (p.His211=)	SPARC	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 732215	NM_003118.4(SPARC):c.513C>G (p.Leu171=)	SPARC	Single nucleotide variant (synonymous variant)	SPARC-related disorder +1 more	GLikely benign
Select item 3049227	NM_003118.4(SPARC):c.387G>A (p.Lys129=)	SPARC	Single nucleotide variant (synonymous variant)	SPARC-related disorder	GLikely benign
Select item 716348	NM_003118.4(SPARC):c.209A>G (p.Asn70Ser)	SPARC (N70S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3030956	NM_003118.4(SPARC):c.209-4A>G	SPARC	Single nucleotide variant (intron variant)	SPARC-related disorder	GLikely benign
Select item 1653930	NM_003118.4(SPARC):c.187G>A (p.Glu63Lys)	SPARC (E62K +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 726331	NM_003118.4(SPARC):c.120+5G>A	SPARC	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign