Related gene-specific medical variations for Gene (Select 79908) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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
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 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 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 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 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 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 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 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 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