"Ambry Genetics"[submitter] AND "OR1L8"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2559818	NM_001004457.2(OR1N2):c.76G>A (p.Glu26Lys)	OR1J2, OR1L8 +1 more (E26K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250016	NM_001004457.2(OR1N2):c.169C>T (p.His57Tyr)	OR1J2, OR1L8 +1 more (H57Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274270	NM_001004457.2(OR1N2):c.250A>T (p.Met84Leu)	OR1J2, OR1L8 +1 more (M84L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603117	NM_001004457.2(OR1N2):c.287C>T (p.Ser96Leu)	OR1J2, OR1L8 +1 more (S96L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297015	NM_001004457.2(OR1N2):c.368A>G (p.Tyr123Cys)	OR1J2, OR1L8 +1 more (Y123C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302603	NM_001004457.2(OR1N2):c.422C>T (p.Pro141Leu)	OR1J2, OR1L8 +1 more (P141L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590759	NM_001004457.2(OR1N2):c.503G>A (p.Arg168His)	OR1J2, OR1L8 +1 more (R168H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401339	NM_001004457.2(OR1N2):c.505G>A (p.Val169Met)	OR1J2, OR1L8 +1 more (V169M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595898	NM_001004457.2(OR1N2):c.516T>G (p.Cys172Trp)	OR1J2, OR1L8 +1 more (C172W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314681	NM_001004457.2(OR1N2):c.536A>G (p.His179Arg)	OR1J2, OR1L8 +1 more (H179R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482708	NM_001004457.2(OR1N2):c.541T>C (p.Tyr181His)	OR1J2, OR1L8 +1 more (Y181H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541154	NM_001004457.2(OR1N2):c.542A>C (p.Tyr181Ser)	OR1J2, OR1L8 +1 more (Y181S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383364	NM_001004457.2(OR1N2):c.566A>G (p.Lys189Arg)	OR1J2, OR1L8 +1 more (K189R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302606	NM_001004457.2(OR1N2):c.568C>T (p.Leu190Phe)	OR1J2, OR1L8 +1 more (L190F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388756	NM_001004457.2(OR1N2):c.569T>C (p.Leu190Pro)	OR1J2, OR1L8 +1 more (L190P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481317	NM_001004457.2(OR1N2):c.725C>A (p.Ser242Tyr)	OR1J2, OR1L8 +1 more (S242Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302605	NM_001004457.2(OR1N2):c.767G>T (p.Gly256Val)	OR1J2, OR1L8 +1 more (G256V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204963	NM_001004457.2(OR1N2):c.846G>A (p.Met282Ile)	OR1J2, OR1L8 +1 more (M282I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212165	NM_001004457.2(OR1N2):c.862C>G (p.Leu288Val)	OR1J2, OR1L8 +1 more (L288V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461772	NM_001004454.2(OR1L8):c.925T>G (p.Ser309Ala)	OR1J2, OR1L8 (S309A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340029	NM_001004454.2(OR1L8):c.736C>T (p.Leu246Phe)	OR1J2, OR1L8 (L246F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302592	NM_001004454.2(OR1L8):c.724T>A (p.Cys242Ser)	OR1J2, OR1L8 (C242S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352399	NM_001004454.2(OR1L8):c.706C>T (p.Arg236Cys)	OR1J2, OR1L8 (R236C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519671	NM_001004454.2(OR1L8):c.497G>A (p.Arg166His)	OR1J2, OR1L8 (R166H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365650	NM_001004454.2(OR1L8):c.496C>A (p.Arg166Ser)	OR1J2, OR1L8 (R166S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204947	NM_001004454.2(OR1L8):c.428T>C (p.Val143Ala)	OR1J2, OR1L8 (V143A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204946	NM_001004454.2(OR1L8):c.424T>C (p.Cys142Arg)	OR1J2, OR1L8 (C142R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271009	NM_001004454.2(OR1L8):c.368G>A (p.Arg123His)	OR1J2, OR1L8 (R123H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204944	NM_001004454.2(OR1L8):c.306G>T (p.Met102Ile)	OR1J2, OR1L8 (M102I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220447	NM_001004454.2(OR1L8):c.256T>A (p.Phe86Ile)	OR1J2, OR1L8 (F86I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546593	NM_001004454.2(OR1L8):c.189C>G (p.Phe63Leu)	OR1J2, OR1L8 (F63L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351235	NM_001004454.2(OR1L8):c.118A>G (p.Ile40Val)	OR1J2, OR1L8 (I40V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598645	NM_001004454.2(OR1L8):c.34G>A (p.Glu12Lys)	OR1J2, OR1L8 (E12K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204945	NM_001004454.2(OR1L8):c.32C>G (p.Ser11Cys)	OR1J2, OR1L8 (S11C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491224	NM_001004454.2(OR1L8):c.5A>G (p.Glu2Gly)	OR1J2, OR1L8 (E2G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 35