BTNL8[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2226861	NM_001040462.3(BTNL8):c.148G>C (p.Ala50Pro)	BTNL8 (A50P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262080	NM_001040462.3(BTNL8):c.169A>G (p.Arg57Gly)	BTNL8 (R57G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398526	NM_001040462.3(BTNL8):c.179T>C (p.Phe60Ser)	BTNL8 (F60S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619634	NM_001040462.3(BTNL8):c.235C>T (p.Pro79Ser)	BTNL8 (P79S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466546	NM_001040462.3(BTNL8):c.278C>T (p.Ala93Val)	BTNL8 (A93V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613211	NM_001040462.3(BTNL8):c.286C>T (p.Arg96Cys)	BTNL8 (R96C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542221	NM_001040462.3(BTNL8):c.484C>G (p.Arg162Gly)	BTNL8 (R162G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550662	NM_001040462.3(BTNL8):c.520G>C (p.Asp174His)	BTNL8 (D49H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386389	NM_001040462.3(BTNL8):c.536C>T (p.Ser179Phe)	BTNL8 (S63F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390795	NM_001040462.3(BTNL8):c.554T>G (p.Met185Arg)	BTNL8 (M69R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2569273	NM_001040462.3(BTNL8):c.565T>G (p.Phe189Val)	BTNL8 (F5V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521109	NM_001040462.3(BTNL8):c.604G>C (p.Gly202Arg)	BTNL8 (G18R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554475	NM_001040462.3(BTNL8):c.626G>A (p.Arg209Gln)	BTNL8 (R25Q +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2364280	NM_001040462.3(BTNL8):c.661G>A (p.Val221Ile)	BTNL8 (V105I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269159	NM_001040462.3(BTNL8):c.688C>T (p.Pro230Ser)	BTNL8 (P46S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613212	NM_001040462.3(BTNL8):c.692T>C (p.Ile231Thr)	BTNL8 (I106T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396089	NM_001040462.3(BTNL8):c.728T>G (p.Leu243Arg)	BTNL8 (L243R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656160	NM_001040462.3(BTNL8):c.801G>A (p.Ala267=)	BTNL8 (G311R)	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2590006	NM_001040462.3(BTNL8):c.887C>T (p.Thr296Met)	BTNL8 (T180M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance