"Ambry Genetics"[submitter] AND "SLAMF7"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2263724	NM_021181.5(SLAMF7):c.227G>T (p.Arg76Leu)	SLAMF7 (R76L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517920	NM_021181.5(SLAMF7):c.482T>C (p.Ile161Thr)	SLAMF7 (I161T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3318770	NM_021181.5(SLAMF7):c.755G>C (p.Arg252Thr)	SLAMF7 (R252T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236461	NM_021181.5(SLAMF7):c.796G>A (p.Asp266Asn)	SLAMF7 (D132N +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162728	NM_021181.5(SLAMF7):c.797A>G (p.Asp266Gly)	SLAMF7 (D132G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588238	NM_021181.5(SLAMF7):c.941A>C (p.Glu314Ala)	SLAMF7 (E183A +5 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3162729	NM_021181.5(SLAMF7):c.956T>G (p.Leu319Arg)	SLAMF7 (L188R +5 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance

ClinVar