Related gene-specific medical variations for Gene (Select 81442) - ClinVar

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Links from Gene

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3303357	NM_001005278.2(OR6N2):c.382C>T (p.Arg128Trp)	OR6N1, OR6N2 (R128W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206567	NM_001005278.2(OR6N2):c.872G>A (p.Ser291Asn)	OR6N1, OR6N2 (S291N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206566	NM_001005278.2(OR6N2):c.781C>T (p.Arg261Trp)	OR6N1, OR6N2 (R261W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206565	NM_001005278.2(OR6N2):c.535T>G (p.Cys179Gly)	OR6N1, OR6N2 (C179G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206564	NM_001005278.2(OR6N2):c.383G>A (p.Arg128Gln)	OR6N1, OR6N2 (R128Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206563	NM_001005278.2(OR6N2):c.282T>A (p.Phe94Leu)	OR6N1, OR6N2 (F94L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206562	NM_001005278.2(OR6N2):c.245T>C (p.Leu82Ser)	OR6N1, OR6N2 (L82S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206561	NM_001005278.2(OR6N2):c.170C>A (p.Thr57Lys)	OR6N1, OR6N2 (T57K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2639480	NM_001005278.2(OR6N2):c.-6-1G>T	OR6N1, OR6N2	Single nucleotide variant (splice acceptor variant)	not provided	GLikely benign
Select item 2639479	NM_001005278.2(OR6N2):c.106C>T (p.Leu36=)	OR6N1, OR6N2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2620790	NM_001005278.2(OR6N2):c.593T>G (p.Val198Gly)	OR6N1, OR6N2 (V198G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457083	NM_001005278.2(OR6N2):c.11A>G (p.Tyr4Cys)	OR6N1, OR6N2 (Y4C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403110	NM_001005278.2(OR6N2):c.431T>C (p.Met144Thr)	OR6N1, OR6N2 (M144T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383395	NM_001005278.2(OR6N2):c.878G>A (p.Arg293His)	OR6N1, OR6N2 (R293H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335741	NM_001005278.2(OR6N2):c.571G>T (p.Asp191Tyr)	OR6N1, OR6N2 (D191Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329421	NM_001005278.2(OR6N2):c.583A>G (p.Asn195Asp)	OR6N1, OR6N2 (N195D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318527	NM_001005278.2(OR6N2):c.458T>A (p.Phe153Tyr)	OR6N1, OR6N2 (F153Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284546	NM_001005278.2(OR6N2):c.289T>C (p.Cys97Arg)	OR6N1, OR6N2 (C97R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281319	NM_001005278.2(OR6N2):c.578C>A (p.Ser193Tyr)	OR6N1, OR6N2 (S193Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205643	NM_001005278.2(OR6N2):c.352A>G (p.Met118Val)	OR6N1, OR6N2 (M118V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 20