"PreventionGenetics, part of Exact Sciences"[submitter] AND "TNFRSF10B - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042611	NM_003842.5(TNFRSF10B):c.*5G>T	TNFRSF10B	Single nucleotide variant (3 prime UTR variant +1 more)	TNFRSF10B-related disorder	GLikely benign
Select item 3053266	NM_003842.5(TNFRSF10B):c.769C>T (p.Arg257Cys)	TNFRSF10B (R228C +1 more)	Single nucleotide variant (missense variant +1 more)	TNFRSF10B-related disorder	GLikely benign
Select item 3055816	NM_003842.5(TNFRSF10B):c.657A>G (p.Thr219=)	TNFRSF10B	Single nucleotide variant (synonymous variant +1 more)	TNFRSF10B-related disorder	GLikely benign
Select item 3059674	NM_003842.5(TNFRSF10B):c.572T>C (p.Val191Ala)	TNFRSF10B (V191A)	Single nucleotide variant (missense variant +1 more)	TNFRSF10B-related disorder	GBenign
Select item 3040635	NM_003842.5(TNFRSF10B):c.300A>G (p.Gly100=)	TNFRSF10B	Single nucleotide variant (synonymous variant +1 more)	TNFRSF10B-related disorder	GLikely benign
Select item 3040322	NM_003842.5(TNFRSF10B):c.279T>C (p.Asp93=)	TNFRSF10B	Single nucleotide variant (synonymous variant +1 more)	TNFRSF10B-related disorder	GLikely benign
Select item 3051063	NM_003842.5(TNFRSF10B):c.270C>T (p.Asp90=)	TNFRSF10B	Single nucleotide variant (synonymous variant +1 more)	TNFRSF10B-related disorder	GLikely benign
Select item 3056241	NM_003842.5(TNFRSF10B):c.200C>T (p.Ala67Val)	TNFRSF10B (A67V)	Single nucleotide variant (missense variant)	TNFRSF10B-related disorder	GBenign
Select item 719596	NM_003842.5(TNFRSF10B):c.168C>T (p.Ile56=)	TNFRSF10B	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign