"Ambry Genetics"[submitter] AND "VSNL1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3189142	NM_003385.5(VSNL1):c.8A>G (p.Lys3Arg)	VSNL1 (K3R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3189141	NM_003385.5(VSNL1):c.187A>G (p.Lys63Glu)	VSNL1 (K63E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550151	NM_003385.5(VSNL1):c.353G>A (p.Arg118Gln)	VSNL1 (R118Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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