"PreventionGenetics, part of Exact Sciences"[submitter] AND "VPS35L"[g - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2672622	NM_020314.7(VPS35L):c.1554G>A (p.Thr518=)	VPS35L	Single nucleotide variant (synonymous variant +1 more)	VPS35L-related condition +2 more	GLikely benign
Select item 2631580	NM_020314.7(VPS35L):c.2161C>T (p.Arg721Cys)	VPS35L (R425C +4 more)	Single nucleotide variant (missense variant +1 more)	VPS35L-related condition	GUncertain significance
Select item 2634212	NM_020314.7(VPS35L):c.2886G>C (p.Arg962Ser)	VPS35L (R666S +4 more)	Single nucleotide variant (missense variant +1 more)	VPS35L-related condition	GUncertain significance

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