"PreventionGenetics, part of Exact Sciences"[submitter] AND "SHPK"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 757037	NM_013276.4(SHPK):c.1122G>A (p.Gly374=)	SHPK	Single nucleotide variant (synonymous variant)	SHPK-related condition +1 more	GLikely benign
Select item 791197	NM_013276.4(SHPK):c.955G>A (p.Ala319Thr)	SHPK (A319T)	Single nucleotide variant (missense variant)	SHPK-related condition +1 more	GBenign
Select item 715311	NM_013276.4(SHPK):c.794A>G (p.Tyr265Cys)	SHPK (Y265C)	Single nucleotide variant (missense variant)	SHPK-related condition +1 more	GBenign

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