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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060083	NM_002658.6(PLAU):c.87G>T (p.Ser29=)	C10orf55, PLAU	Single nucleotide variant (non-coding transcript variant +2 more)	C10orf55-related disorder	GLikely benign
Select item 300743	NM_002658.6(PLAU):c.162A>G (p.Pro54=)	C10orf55, PLAU	Single nucleotide variant (synonymous variant +1 more)	Quebec platelet disorder +2 more	GBenign/Likely benign
Select item 3055508	NM_002658.6(PLAU):c.194-7C>G	C10orf55, PLAU	Single nucleotide variant (intron variant)	C10orf55-related disorder	GLikely benign
Select item 3057907	NM_002658.6(PLAU):c.423G>A (p.Leu141=)	C10orf55, LOC126860960 +1 more	Single nucleotide variant (synonymous variant)	PLAU-related disorder	GLikely benign
Select item 2637149	NM_002658.6(PLAU):c.861G>T (p.Arg287Ser)	C10orf55, PLAU (R201S +2 more)	Single nucleotide variant (missense variant)	PLAU-related disorder	GUncertain significance
Select item 300758	NM_002658.6(PLAU):c.1048T>C (p.Tyr350His)	C10orf55, PLAU (Y350H +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign

ClinVar