Related gene-specific medical variations for Gene (Select 23538) - ClinVar

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Links from Gene

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3303051	NM_012375.3(OR52A1):c.692T>C (p.Leu231Ser)	LOC110011217, OR52A1 (L231S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3303050	NM_012375.3(OR52A1):c.133T>G (p.Ser45Ala)	LOC110011217, OR52A1 (S45A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3303049	NM_012375.3(OR52A1):c.275C>T (p.Pro92Leu)	LOC110011217, OR52A1 (P92L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3303048	NM_012375.3(OR52A1):c.554T>C (p.Met185Thr)	LOC110011217, OR52A1 (M185T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3303047	NM_012375.3(OR52A1):c.820T>C (p.Tyr274His)	LOC110011217, OR52A1 (Y274H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205894	NM_012375.3(OR52A1):c.907C>T (p.Arg303Cys)	LOC110011217, OR52A1 (R303C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205893	NM_012375.3(OR52A1):c.862C>T (p.Pro288Ser)	LOC110011217, OR52A1 (P288S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205892	NM_012375.3(OR52A1):c.832C>G (p.Leu278Val)	LOC110011217, OR52A1 (L278V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205891	NM_012375.3(OR52A1):c.821A>G (p.Tyr274Cys)	LOC110011217, OR52A1 (Y274C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205890	NM_012375.3(OR52A1):c.734T>C (p.Ile245Thr)	LOC110011217, OR52A1 (I245T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205889	NM_012375.3(OR52A1):c.725A>G (p.Asn242Ser)	LOC110011217, OR52A1 (N242S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205887	NM_012375.3(OR52A1):c.266T>G (p.Phe89Cys)	LOC110011217, OR52A1 (F89C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205886	NM_012375.3(OR52A1):c.221C>T (p.Ala74Val)	LOC110011217, OR52A1 (A74V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205885	NM_012375.3(OR52A1):c.202C>G (p.Leu68Val)	LOC110011217, OR52A1 (L68V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205884	NM_012375.3(OR52A1):c.110A>T (p.Tyr37Phe)	LOC110011217, OR52A1 (Y37F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612348	NM_012375.3(OR52A1):c.203T>C (p.Leu68Pro)	LOC110011217, OR52A1 (L68P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555748	NM_012375.3(OR52A1):c.568C>G (p.Leu190Val)	LOC110011217, OR52A1 (L190V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528495	NM_012375.3(OR52A1):c.71C>T (p.Ser24Phe)	LOC110011217, OR52A1 (S24F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464479	NM_012375.3(OR52A1):c.175G>A (p.Glu59Lys)	LOC110011217, OR52A1 (E59K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462556	NM_012375.3(OR52A1):c.607T>A (p.Leu203Met)	LOC110011217, OR52A1 (L203M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394897	NM_012375.3(OR52A1):c.256A>G (p.Ile86Val)	LOC110011217, OR52A1 (I86V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283779	NM_012375.3(OR52A1):c.521C>A (p.Thr174Lys)	LOC110011217, OR52A1 (T174K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282747	NM_012375.3(OR52A1):c.746G>A (p.Cys249Tyr)	LOC110011217, OR52A1 (C249Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271594	NM_012375.3(OR52A1):c.772G>A (p.Ala258Thr)	LOC110011217, OR52A1 (A258T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221442	NM_012375.3(OR52A1):c.736G>T (p.Ala246Ser)	LOC110011217, OR52A1 (A246S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212124	NM_012375.3(OR52A1):c.502C>T (p.Arg168Trp)	LOC110011217, OR52A1 (R168W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204706	NM_012375.3(OR52A1):c.859C>G (p.Pro287Ala)	LOC110011217, OR52A1 (P287A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 27