"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CASP8"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2651816	NM_001228.5(CASP8):c.-26-8200T>G	CASP8, LOC128772255	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 870948	NM_001228.5(CASP8):c.-26-8076G>A	CASP8, LOC129935411	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 870949	NM_001372051.1(CASP8):c.-15C>A	CASP8 (L55M)	Single nucleotide variant (5 prime UTR variant +3 more)	not provided	GUncertain significance
Select item 333498	NM_001372051.1(CASP8):c.339C>T (p.Ser113=)	CASP8	Single nucleotide variant (synonymous variant +2 more)	Familial cancer of breast +4 more	GBenign/Likely benign
Select item 333499	NM_001372051.1(CASP8):c.432A>G (p.Ile144Met)	CASP8 (I144M +3 more)	Single nucleotide variant (missense variant +2 more)	CASP8-related condition +2 more	GUncertain significance
Select item 809140	NM_001372051.1(CASP8):c.1129G>A (p.Glu377Lys)	CASP8 (E377K +13 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance

ClinVar