"Ambry Genetics"[submitter] AND "TNFSF9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2380113	NM_003811.4(TNFSF9):c.16G>A (p.Asp6Asn)	LOC130063302, TNFSF9 (D6N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278704	NM_003811.4(TNFSF9):c.76G>C (p.Val26Leu)	TNFSF9 (V26L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2531787	NM_003811.4(TNFSF9):c.154C>T (p.Pro52Ser)	TNFSF9 (P52S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253056	NM_003811.4(TNFSF9):c.331A>G (p.Ser111Gly)	TNFSF9 (S111G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374260	NM_003811.4(TNFSF9):c.362C>T (p.Thr121Met)	TNFSF9 (T121M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514778	NM_003811.4(TNFSF9):c.673G>A (p.Ala225Thr)	LOC130063305, TNFSF9 (A225T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar