TNFRSF1B[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180267	NM_001066.3(TNFRSF1B):c.80T>C (p.Val27Ala)	TNFRSF1B (V27A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 738058	NM_001066.3(TNFRSF1B):c.138T>C (p.Tyr46=)	TNFRSF1B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2405076	NM_001066.3(TNFRSF1B):c.497C>T (p.Pro166Leu)	TNFRSF1B (P166L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260167	NM_001066.3(TNFRSF1B):c.497C>G (p.Pro166Arg)	TNFRSF1B (P166R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 731198	NM_001066.3(TNFRSF1B):c.543C>T (p.Pro181=)	TNFRSF1B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3327518	NM_001066.3(TNFRSF1B):c.554G>C (p.Cys185Ser)	TNFRSF1B (C185S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 734527	NM_001066.3(TNFRSF1B):c.559G>A (p.Val187Met)	TNFRSF1B (V187M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1048802	NM_001066.3(TNFRSF1B):c.587T>G (p.Met196Arg)	TNFRSF1B (M196R)	Single nucleotide variant (missense variant)	Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR2 +2 more	GUncertain significance
Select item 2279536	NM_001066.3(TNFRSF1B):c.602C>G (p.Thr201Arg)	TNFRSF1B (T201R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 744556	NM_001066.3(TNFRSF1B):c.608C>T (p.Thr203Met)	TNFRSF1B (T203M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3180266	NM_001066.3(TNFRSF1B):c.670T>C (p.Ser224Pro)	TNFRSF1B (S224P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250250	NM_001066.3(TNFRSF1B):c.698C>A (p.Pro233His)	TNFRSF1B (P233H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 763361	NM_001066.3(TNFRSF1B):c.768C>T (p.Gly256=)	TNFRSF1B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 730777	NM_001066.3(TNFRSF1B):c.787+7C>A	TNFRSF1B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 780214	NM_001066.3(TNFRSF1B):c.791T>C (p.Leu264Pro)	TNFRSF1B (L264P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 779853	NM_001066.3(TNFRSF1B):c.919A>G (p.Lys307Glu)	TNFRSF1B (K307E)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2590817	NM_001066.3(TNFRSF1B):c.925C>T (p.Arg309Trp)	TNFRSF1B (R309W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180268	NM_001066.3(TNFRSF1B):c.955C>G (p.Leu319Val)	TNFRSF1B (L319V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 762259	NM_001066.3(TNFRSF1B):c.972G>C (p.Pro324=)	TNFRSF1B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2316833	NM_001066.3(TNFRSF1B):c.1041G>C (p.Gln347His)	TNFRSF1B (Q347H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180265	NM_001066.3(TNFRSF1B):c.1062G>C (p.Glu354Asp)	TNFRSF1B (E354D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214715	NM_001066.3(TNFRSF1B):c.1084C>T (p.Arg362Trp)	TNFRSF1B (R362W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327517	NM_001066.3(TNFRSF1B):c.1189T>G (p.Cys397Gly)	TNFRSF1B (C397G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300771	NM_001066.3(TNFRSF1B):c.1283G>A (p.Cys428Tyr)	TNFRSF1B (C428Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267742	NM_001066.3(TNFRSF1B):c.1303G>A (p.Glu435Lys)	TNFRSF1B (E435K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1048803	NM_001066.3(TNFRSF1B):c.*215C>T	TNFRSF1B	Single nucleotide variant (3 prime UTR variant)	Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR3 +2 more	GUncertain significance

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Items: 26