"Ambry Genetics"[submitter] AND "TNFRSF8"[gene] - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327534	NM_001243.5(TNFRSF8):c.22C>G (p.Leu8Val)	LOC129929439, TNFRSF8 (L8V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363513	NM_001243.5(TNFRSF8):c.235G>A (p.Asp79Asn)	TNFRSF8 (D79N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3180302	NM_001243.5(TNFRSF8):c.355G>T (p.Val119Phe)	TNFRSF8 (V119F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343477	NM_001243.5(TNFRSF8):c.458C>T (p.Ser153Phe)	TNFRSF8 (S153F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357626	NM_001243.5(TNFRSF8):c.488C>T (p.Pro163Leu)	TNFRSF8 (P52L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180303	NM_001243.5(TNFRSF8):c.542C>T (p.Pro181Leu)	TNFRSF8 (P70L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2390270	NM_001243.5(TNFRSF8):c.635C>T (p.Pro212Leu)	TNFRSF8 (P101L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607265	NM_001243.5(TNFRSF8):c.686C>G (p.Pro229Arg)	TNFRSF8 (P229R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180305	NM_001243.5(TNFRSF8):c.753C>A (p.Asp251Glu)	TNFRSF8 (D140E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242047	NM_001243.5(TNFRSF8):c.754G>A (p.Glu252Lys)	TNFRSF8 (E141K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244936	NM_001243.5(TNFRSF8):c.764G>A (p.Arg255His)	TNFRSF8 (R255H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180306	NM_001243.5(TNFRSF8):c.770C>T (p.Thr257Met)	TNFRSF8 (T257M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225523	NM_001243.5(TNFRSF8):c.778G>A (p.Val260Met)	TNFRSF8 (V149M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180307	NM_001243.5(TNFRSF8):c.809A>C (p.Lys270Thr)	TNFRSF8 (K159T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180308	NM_001243.5(TNFRSF8):c.812C>T (p.Thr271Met)	TNFRSF8 (T271M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517551	NM_001243.5(TNFRSF8):c.835C>T (p.Arg279Cys)	TNFRSF8 (R168C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373101	NM_001243.5(TNFRSF8):c.844G>A (p.Glu282Lys)	TNFRSF8 (E171K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210214	NM_001243.5(TNFRSF8):c.851G>A (p.Arg284Gln)	TNFRSF8 (R284Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537565	NM_001243.5(TNFRSF8):c.854C>T (p.Pro285Leu)	TNFRSF8 (P174L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180309	NM_001243.5(TNFRSF8):c.864C>G (p.Ile288Met)	TNFRSF8 (I288M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478757	NM_001243.5(TNFRSF8):c.880A>G (p.Thr294Ala)	TNFRSF8 (T294A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618317	NM_001243.5(TNFRSF8):c.896G>A (p.Arg299His)	TNFRSF8 (R299H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180310	NM_001243.5(TNFRSF8):c.913A>G (p.Ile305Val)	TNFRSF8 (I305V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327530	NM_001243.5(TNFRSF8):c.929C>T (p.Thr310Met)	TNFRSF8 (T310M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2507652	NM_001243.5(TNFRSF8):c.982C>A (p.Pro328Thr)	TNFRSF8 (P217T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180311	NM_001243.5(TNFRSF8):c.998C>A (p.Pro333Gln)	TNFRSF8 (P222Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327533	NM_001243.5(TNFRSF8):c.1001A>G (p.Asp334Gly)	TNFRSF8 (D223G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 252571	NM_001243.5(TNFRSF8):c.1043C>T (p.Thr348Ile)	TNFRSF8 (T348I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327529	NM_001243.5(TNFRSF8):c.1108G>A (p.Ala370Thr)	TNFRSF8 (A259T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514636	NM_001243.5(TNFRSF8):c.1193T>C (p.Val398Ala)	TNFRSF8 (V398A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327531	NM_001243.5(TNFRSF8):c.1198G>A (p.Gly400Ser)	TNFRSF8 (G289S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553462	NM_001243.5(TNFRSF8):c.1351G>A (p.Ala451Thr)	TNFRSF8 (A339T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2598187	NM_001243.5(TNFRSF8):c.1373C>T (p.Ala458Val)	TNFRSF8 (A346V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180298	NM_001243.5(TNFRSF8):c.1423G>A (p.Val475Met)	TNFRSF8 (V475M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457328	NM_001243.5(TNFRSF8):c.1469C>T (p.Pro490Leu)	TNFRSF8 (P378L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221659	NM_001243.5(TNFRSF8):c.1506G>C (p.Glu502Asp)	TNFRSF8 (E390D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180299	NM_001243.5(TNFRSF8):c.1604C>A (p.Pro535Gln)	TNFRSF8 (P423Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386930	NM_001243.5(TNFRSF8):c.1622C>T (p.Ala541Val)	TNFRSF8 (A429V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3180300	NM_001243.5(TNFRSF8):c.1639G>A (p.Glu547Lys)	TNFRSF8 (E435K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180301	NM_001243.5(TNFRSF8):c.1661C>T (p.Ala554Val)	TNFRSF8 (A442V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3327532	NM_001243.5(TNFRSF8):c.1720G>A (p.Asp574Asn)	TNFRSF8 (D462N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316980	NM_001243.5(TNFRSF8):c.1726A>T (p.Met576Leu)	TNFRSF8 (M464L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616910	NM_001243.5(TNFRSF8):c.1741G>A (p.Glu581Lys)	TNFRSF8 (E469K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 43