"Fulgent Genetics, Fulgent Genetics"[submitter] AND "VPS35"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 30196	NM_018206.6(VPS35):c.1858G>A (p.Asp620Asn)	VPS35 (D620N)	Single nucleotide variant (missense variant)	Parkinson disease 17 +1 more	GPathogenic
Select item 571710	NM_018206.6(VPS35):c.1313G>A (p.Cys438Tyr)	VPS35 (C438Y)	Single nucleotide variant (missense variant)	Parkinson disease 17	GUncertain significance
Select item 1521803	NM_018206.6(VPS35):c.1262T>A (p.Phe421Tyr)	VPS35 (F421Y)	Single nucleotide variant (missense variant)	Parkinson disease 17	GUncertain significance
Select item 1608805	NM_018206.6(VPS35):c.915-16T>G	VPS35	Single nucleotide variant (intron variant)	Parkinson disease 17	GBenign/Likely benign
Select item 319294	NM_018206.6(VPS35):c.851G>A (p.Arg284Gln)	VPS35 (R284Q)	Single nucleotide variant (missense variant)	Parkinson disease 17	GUncertain significance
Select item 704148	NM_018206.6(VPS35):c.834T>C (p.Thr278=)	VPS35	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 319297	NM_018206.6(VPS35):c.-19C>T	VPS35	Single nucleotide variant (5 prime UTR variant)	Parkinson disease 17	GUncertain significance

ClinVar