"Ambry Genetics"[submitter] AND "LPAR6"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3291158	NM_001162498.3(LPAR6):c.964G>T (p.Ala322Ser)	LPAR6, RB1 (A322S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3119727	NM_001162498.3(LPAR6):c.933A>T (p.Arg311Ser)	LPAR6, RB1 (R311S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2206065	NM_001162498.3(LPAR6):c.815T>C (p.Met272Thr)	LPAR6, RB1 (M272T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2493267	NM_001162498.3(LPAR6):c.794T>C (p.Val265Ala)	LPAR6, RB1 (V265A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2491821	NM_001162498.3(LPAR6):c.728T>C (p.Val243Ala)	LPAR6, RB1 (V243A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2275172	NM_001162498.3(LPAR6):c.709A>G (p.Ile237Val)	LPAR6, RB1 (I237V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2287621	NM_001162498.3(LPAR6):c.707T>C (p.Ile236Thr)	LPAR6, RB1 (I236T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2287928	NM_001162498.3(LPAR6):c.697G>A (p.Val233Ile)	LPAR6, RB1 (V233I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2512462	NM_001162498.3(LPAR6):c.626A>G (p.Lys209Arg)	LPAR6, RB1 (K209R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2406764	NM_001162498.3(LPAR6):c.571G>C (p.Val191Leu)	LPAR6, RB1 (V191L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2471064	NM_001162498.3(LPAR6):c.474C>A (p.His158Gln)	LPAR6, RB1 (H158Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2402771	NM_001162498.3(LPAR6):c.402G>C (p.Lys134Asn)	LPAR6, RB1 (K134N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2318482	NM_001162498.3(LPAR6):c.353T>G (p.Ile118Ser)	LPAR6, RB1 (I118S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3119724	NM_001162498.3(LPAR6):c.116T>C (p.Ile39Thr)	LPAR6, RB1 (I39T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2282236	NM_001162498.3(LPAR6):c.104A>G (p.Asn35Ser)	LPAR6, RB1 (N35S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2207808	NM_001162498.3(LPAR6):c.83T>C (p.Phe28Ser)	LPAR6, RB1 (F28S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3119726	NM_001162498.3(LPAR6):c.49T>C (p.Tyr17His)	LPAR6, RB1 (Y17H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2353884	NM_001162498.3(LPAR6):c.31T>C (p.Tyr11His)	LPAR6, RB1 (Y11H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance