"Ambry Genetics"[submitter] AND "TNFSF14"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2241580	NM_001376887.1(TNFSF14):c.565C>T (p.Arg189Trp)	TNFSF14 (R189W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2274763	NM_001376887.1(TNFSF14):c.319G>A (p.Gly107Ser)	TNFSF14 (G107S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2237713	NM_001376887.1(TNFSF14):c.317C>T (p.Thr106Ile)	TNFSF14 (T106I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263627	NM_001376887.1(TNFSF14):c.229G>A (p.Ala77Thr)	TNFSF14 (A41T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255103	NM_001376887.1(TNFSF14):c.134T>C (p.Leu45Ser)	LOC130063326, TNFSF14 (L45S)	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2570209	NM_001376887.1(TNFSF14):c.92A>G (p.Gln31Arg)	LOC130063326, TNFSF14 (Q31R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign

ClinVar