"Ambry Genetics"[submitter] AND "TNFAIP2"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2298886	NM_006291.4(TNFAIP2):c.58T>C (p.Tyr20His)	TNFAIP2 (Y20H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2622320	NM_006291.4(TNFAIP2):c.67G>A (p.Glu23Lys)	TNFAIP2 (E23K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344629	NM_006291.4(TNFAIP2):c.197C>A (p.Ala66Asp)	TNFAIP2 (A66D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527536	NM_006291.4(TNFAIP2):c.199G>A (p.Gly67Arg)	TNFAIP2 (G67R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2272344	NM_006291.4(TNFAIP2):c.221G>A (p.Gly74Asp)	TNFAIP2 (G74D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2483482	NM_006291.4(TNFAIP2):c.224C>T (p.Pro75Leu)	TNFAIP2 (P75L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343316	NM_006291.4(TNFAIP2):c.240G>C (p.Glu80Asp)	TNFAIP2 (E80D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2267299	NM_006291.4(TNFAIP2):c.271C>G (p.Leu91Val)	TNFAIP2 (L91V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534688	NM_006291.4(TNFAIP2):c.338T>C (p.Val113Ala)	TNFAIP2 (V113A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2534689	NM_006291.4(TNFAIP2):c.344A>C (p.Glu115Ala)	TNFAIP2 (E115A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534690	NM_006291.4(TNFAIP2):c.388G>C (p.Glu130Gln)	TNFAIP2 (E130Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534691	NM_006291.4(TNFAIP2):c.389A>T (p.Glu130Val)	TNFAIP2 (E130V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2513000	NM_006291.4(TNFAIP2):c.415G>C (p.Val139Leu)	TNFAIP2 (V139L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464081	NM_006291.4(TNFAIP2):c.421C>T (p.Arg141Trp)	TNFAIP2 (R141W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2310153	NM_006291.4(TNFAIP2):c.521G>A (p.Gly174Glu)	TNFAIP2 (G174E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477022	NM_006291.4(TNFAIP2):c.544C>T (p.Arg182Cys)	TNFAIP2 (R182C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612585	NM_006291.4(TNFAIP2):c.713T>G (p.Leu238Arg)	TNFAIP2 (L238R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2358933	NM_006291.4(TNFAIP2):c.761A>G (p.His254Arg)	TNFAIP2 (H254R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292776	NM_006291.4(TNFAIP2):c.823T>G (p.Tyr275Asp)	TNFAIP2 (Y275D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236335	NM_006291.4(TNFAIP2):c.901G>T (p.Gly301Cys)	TNFAIP2 (G301C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2496576	NM_006291.4(TNFAIP2):c.1067G>A (p.Cys356Tyr)	TNFAIP2 (C356Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2246407	NM_006291.4(TNFAIP2):c.1217A>G (p.Asn406Ser)	TNFAIP2 (N406S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2241171	NM_006291.4(TNFAIP2):c.1311G>C (p.Glu437Asp)	TNFAIP2 (E437D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345673	NM_006291.4(TNFAIP2):c.1442C>T (p.Thr481Met)	TNFAIP2 (T481M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301871	NM_006291.4(TNFAIP2):c.1450C>T (p.Arg484Cys)	TNFAIP2 (R484C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238292	NM_006291.4(TNFAIP2):c.1667A>G (p.Asn556Ser)	TNFAIP2 (N556S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399724	NM_006291.4(TNFAIP2):c.1711G>T (p.Ala571Ser)	TNFAIP2 (A571S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460456	NM_006291.4(TNFAIP2):c.1757G>A (p.Arg586His)	TNFAIP2 (R586H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2405671	NM_006291.4(TNFAIP2):c.1940T>G (p.Leu647Arg)	TNFAIP2 (L647R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 29