TNFSF4[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180336	NM_003326.5(TNFSF4):c.499G>A (p.Gly167Ser)	TNFSF4 (G117S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 747383	NM_003326.5(TNFSF4):c.478C>T (p.Leu160=)	TNFSF4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2337049	NM_003326.5(TNFSF4):c.385C>G (p.Leu129Val)	TNFSF4 (L129V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334384	NM_003326.5(TNFSF4):c.347G>A (p.Ser116Asn)	TNFSF4 (S66N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334228	NM_003326.5(TNFSF4):c.262G>A (p.Val88Met)	TNFSF4 (V38M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 772822	NM_003326.5(TNFSF4):c.186C>T (p.Ile62=)	TNFSF4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2405313	NM_003326.5(TNFSF4):c.164G>A (p.Arg55Gln)	TNFSF4 (R55Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 979308	GRCh37/hg19 1q25.1(chr1:173047673-173339681)x1	TNFSF4	Copy number loss	not provided	GUncertain significance
Select item 688914	GRCh37/hg19 1q25.1(chr1:173036654-173333855)x1	TNFSF4	Copy number loss	not provided	GUncertain significance
Select item 565197	GRCh37/hg19 1q25.1(chr1:173064278-173167101)x1	TNFSF4	Copy number loss	not provided	GLikely benign