"PreventionGenetics, part of Exact Sciences"[submitter] AND "SP8"[gene - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042795	NM_182700.6(SP8):c.1485G>A (p.Leu495=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3048085	NM_182700.6(SP8):c.1296G>A (p.Lys432=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3043995	NM_182700.6(SP8):c.1254C>T (p.Ser418=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GBenign
Select item 2408943	NM_182700.6(SP8):c.991G>A (p.Ala331Thr)	SP8 (A313T +1 more)	Single nucleotide variant (missense variant)	SP8-related condition +1 more	GConflicting classifications of pathogenicity
Select item 3054534	NM_182700.6(SP8):c.909A>G (p.Pro303=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 709118	NM_182700.6(SP8):c.798C>T (p.Leu266=)	SP8	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3033321	NM_182700.6(SP8):c.510G>T (p.Ser170=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GBenign
Select item 3047108	NM_182700.6(SP8):c.475_495del (p.Gly159_Gly165del)	SP8	Deletion (inframe deletion)	SP8-related condition	GLikely benign
Select item 3056693	NM_182700.6(SP8):c.480G>T (p.Gly160=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3041753	NM_182700.6(SP8):c.480G>C (p.Gly160=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3042037	NM_182700.6(SP8):c.453T>C (p.Val151=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3038098	NM_182700.6(SP8):c.417C>G (p.Phe139Leu)	SP8 (F121L +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3041967	NM_182700.6(SP8):c.393A>C (p.Ala131=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 2657336	NM_182700.6(SP8):c.375CGC[7] (p.Ala134_Ser135insAla)	SP8	Microsatellite (inframe_insertion)	SP8-related condition +1 more	GLikely benign
Select item 3050029	NM_182700.6(SP8):c.372A>C (p.Ala124=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3042647	NM_182700.6(SP8):c.294G>A (p.Ala98=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3045932	NM_182700.6(SP8):c.291C>T (p.Ala97=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3041945	NM_182700.6(SP8):c.288T>C (p.Ala96=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3037997	NM_182700.6(SP8):c.288T>A (p.Ala96=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 2657337	NM_182700.6(SP8):c.288T>G (p.Ala96=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition +1 more	GLikely benign
Select item 3038233	NM_182700.6(SP8):c.279A>T (p.Ala93=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3042421	NM_182700.6(SP8):c.276A>C (p.Ala92=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3038122	NM_182700.6(SP8):c.276A>T (p.Ala92=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3042119	NM_182700.6(SP8):c.267G>A (p.Ala89=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3041751	NM_182700.6(SP8):c.261T>C (p.Ala87=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign
Select item 3039746	NM_182700.6(SP8):c.228G>T (p.Gly76=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GBenign
Select item 3034616	NM_182700.6(SP8):c.223T>A (p.Ser75Thr)	SP8 (S57T +1 more)	Single nucleotide variant (missense variant)	SP8-related condition	GBenign
Select item 3061737	NM_182700.6(SP8):c.96G>A (p.Pro32=)	SP8	Single nucleotide variant (synonymous variant)	SP8-related condition	GLikely benign

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Items: 28