"Laboratory for Molecular Medicine, Mass General Brigham Personalized - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 330156	NM_001127255.2(NLRP7):c.2775A>G (p.Ala925=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 330158	NM_001127255.2(NLRP7):c.2682T>C (p.Tyr894=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 330172	NM_001127255.2(NLRP7):c.1137G>A (p.Lys379=)	NLRP7	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 330176	NM_001127255.2(NLRP7):c.955G>A (p.Val319Ile)	NLRP7 (V319I)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 330183	NM_001127255.2(NLRP7):c.390G>A (p.Gln130=)	NLRP7	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 97796	NM_001127255.2(NLRP7):c.336dup (p.Glu113Glyfs)	NLRP7 (E113fs)	Duplication (frameshift variant)	Hydatidiform mole	GPathogenic

ClinVar