"Fulgent Genetics, Fulgent Genetics"[submitter] AND "TNFRSF4"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1165295	NM_003327.4(TNFRSF4):c.371-16C>T	TNFRSF4	Single nucleotide variant (intron variant)	Combined immunodeficiency due to OX40 deficiency +1 more	GBenign/Likely benign
Select item 580337	NM_003327.4(TNFRSF4):c.146-2A>G	TNFRSF4	Single nucleotide variant (splice acceptor variant)	Combined immunodeficiency due to OX40 deficiency	GUncertain significance