"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "TNFRSF1A"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2538011	NM_001065.4(TNFRSF1A):c.1228C>T (p.Arg410Cys)	TNFRSF1A (R302C +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2683182	NM_001065.4(TNFRSF1A):c.918C>A (p.Asn306Lys)	TNFRSF1A (N153K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 546693	NM_001065.4(TNFRSF1A):c.887G>C (p.Ser296Thr)	TNFRSF1A (S296T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1694064	NM_001065.4(TNFRSF1A):c.393_394insCTGGTGCTTCCTGCAGCCACACACGGTGTCCCGGT (p.Tyr132fs)	TNFRSF1A (Y132fs +1 more)	Insertion (frameshift variant +2 more)	not provided	GUncertain significance
Select item 2683183	NM_001065.4(TNFRSF1A):c.373T>G (p.Cys125Gly)	TNFRSF1A (C125G +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 97682	NM_001065.4(TNFRSF1A):c.283C>T (p.His95Tyr)	TNFRSF1A (H95Y)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 1163932	NM_001065.4(TNFRSF1A):c.122A>T (p.Asp41Val)	TNFRSF1A (D41V)	Single nucleotide variant (missense variant +3 more)	not provided	GUncertain significance

ClinVar