"Ambry Genetics"[submitter] AND "BTNL8"[gene] - ClinVar

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Items: 31

	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 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
Select item 2380416	NM_001040462.3(BTNL8):c.1003A>G (p.Ser335Gly)	BTNL8, LOC126807633 (S151G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477960	NM_001040462.3(BTNL8):c.1039G>A (p.Gly347Arg)	BTNL8, LOC126807633 (G347R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352171	NM_001040462.3(BTNL8):c.1063G>A (p.Val355Met)	BTNL8, LOC126807633 (V230M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302862	NM_001040462.3(BTNL8):c.1105G>A (p.Val369Met)	BTNL8, LOC126807633 (V244M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412312	NM_001040462.3(BTNL8):c.1148A>G (p.Asn383Ser)	BTNL8, LOC126807633 (N258S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262081	NM_001040462.3(BTNL8):c.1232T>A (p.Leu411Gln)	BTNL8, LOC126807633 (L295Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476758	NM_001040462.3(BTNL8):c.1249A>G (p.Thr417Ala)	BTNL8, LOC126807633 (T233A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234033	NM_001040462.3(BTNL8):c.1366C>T (p.Pro456Ser)	BTNL8, LOC126807633 (P272S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234228	NM_001040462.3(BTNL8):c.1370T>C (p.Ile457Thr)	BTNL8, LOC126807633 (I332T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236851	NM_001040462.3(BTNL8):c.1387A>T (p.Thr463Ser)	BTNL8, LOC126807633 (T279S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369916	NM_001040462.3(BTNL8):c.1423G>A (p.Ala475Thr)	BTNL8, LOC126807633 (A350T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359477	NM_001040462.3(BTNL8):c.1475C>T (p.Thr492Met)	BTNL8, LOC126807633 (T367M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513658	NM_001040462.3(BTNL8):c.1499T>G (p.Met500Arg)	BTNL8, LOC126807633 (M375R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 31