Related gene-specific medical variations for Gene (Select 26246) - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3205178	NM_001385855.1(OR2L2):c.814A>G (p.Ile272Val)	OR2L13, OR2L2 (I272V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3205177	NM_001385855.1(OR2L2):c.64A>T (p.Ile22Phe)	OR2L13, OR2L2 (I22F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600888	NM_001385855.1(OR2L2):c.62G>A (p.Arg21Lys)	OR2L13, OR2L2 (R21K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599525	NM_001385855.1(OR2L2):c.499T>C (p.Tyr167His)	OR2L13, OR2L2 (Y167H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593702	NM_001385855.1(OR2L2):c.169C>T (p.Pro57Ser)	OR2L13, OR2L2 (P57S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559100	NM_001385855.1(OR2L2):c.887T>C (p.Val296Ala)	OR2L13, OR2L2 (V296A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540824	NM_001385855.1(OR2L2):c.58T>C (p.Ser20Pro)	OR2L13, OR2L2 (S20P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509549	NM_001385855.1(OR2L2):c.307T>G (p.Phe103Val)	OR2L13, OR2L2 (F103V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401895	NM_001385855.1(OR2L2):c.217A>C (p.Ile73Leu)	OR2L13, OR2L2 (I73L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399246	NM_001385855.1(OR2L2):c.89T>C (p.Ile30Thr)	OR2L13, OR2L2 (I30T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392516	NM_001385855.1(OR2L2):c.408C>A (p.Ser136Arg)	OR2L13, OR2L2 (S136R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392515	NM_001385855.1(OR2L2):c.405A>G (p.Ile135Met)	OR2L13, OR2L2 (I135M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2377006	NM_001385855.1(OR2L2):c.919A>G (p.Ile307Val)	OR2L13, OR2L2 (I307V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371507	NM_001385855.1(OR2L2):c.226A>G (p.Ile76Val)	OR2L13, OR2L2 (I76V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368401	NM_001385855.1(OR2L2):c.778C>T (p.Arg260Cys)	OR2L13, OR2L2 (R260C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366800	NM_001385855.1(OR2L2):c.650A>G (p.Tyr217Cys)	OR2L13, OR2L2 (Y217C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363630	NM_001385855.1(OR2L2):c.322G>A (p.Val108Ile)	OR2L13, OR2L2 (V108I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304051	NM_001385855.1(OR2L2):c.886G>A (p.Val296Met)	OR2L13, OR2L2 (V296M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2280127	NM_001385855.1(OR2L2):c.439T>C (p.Ser147Pro)	OR2L13, OR2L2 (S147P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275219	NM_001385855.1(OR2L2):c.541C>T (p.Pro181Ser)	OR2L13, OR2L2 (P181S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243741	NM_001385855.1(OR2L2):c.935T>G (p.Met312Arg)	OR2L13, OR2L2 (M312R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219024	NM_001385855.1(OR2L2):c.810C>A (p.Asp270Glu)	OR2L13, OR2L2 (D270E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206606	NM_001385855.1(OR2L2):c.826T>G (p.Phe276Val)	OR2L13, OR2L2 (F276V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 23