"Fulgent Genetics, Fulgent Genetics"[submitter] AND "TNFRSF13B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 538709	NM_012452.3(TNFRSF13B):c.706G>T (p.Glu236Ter)	TNFRSF13B (E236*)	Single nucleotide variant (nonsense)	Immunodeficiency, common variable, 2 +2 more	GUncertain significance
Select item 1031204	NM_012452.3(TNFRSF13B):c.693C>G (p.Ser231Arg)	TNFRSF13B (S231R)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 2 +2 more	GUncertain significance
Select item 538714	NM_012452.3(TNFRSF13B):c.641T>C (p.Met214Thr)	TNFRSF13B (M214T)	Single nucleotide variant (missense variant)	Immunoglobulin A deficiency 2 +1 more	GUncertain significance
Select item 840913	NM_012452.3(TNFRSF13B):c.214C>T (p.Arg72Cys)	TNFRSF13B (R72C)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1455440	NM_012452.3(TNFRSF13B):c.61+1G>A	TNFRSF13B	Single nucleotide variant (splice donor variant)	Immunodeficiency, common variable, 2 +1 more	GPathogenic/Likely pathogenic
Select item 636449	NM_012452.3(TNFRSF13B):c.53A>G (p.Glu18Gly)	TNFRSF13B (E18G)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance

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