CD160[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140295	NM_007053.4(CD160):c.55G>A (p.Val19Met)	CD160 (V19M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264719	NM_007053.4(CD160):c.116G>A (p.Arg39Gln)	CD160 (R39Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 718727	NM_007053.4(CD160):c.250G>A (p.Gly84Arg)	CD160 (G84R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2412299	NM_007053.4(CD160):c.317A>G (p.His106Arg)	CD160 (H106R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140294	NM_007053.4(CD160):c.350A>G (p.Gln117Arg)	CD160 (Q117R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512734	NM_007053.4(CD160):c.364C>T (p.Arg122Cys)	CD160 (R122C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593395	NM_007053.4(CD160):c.452T>A (p.Phe151Tyr)	CD160 (F151Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar