"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 97735	NM_001127255.2(NLRP7):c.2095G>A (p.Val699Ile)	NCR1, NLRP7 (V699I +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 97734	NM_001127255.2(NLRP7):c.2094C>T (p.His698=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 892832	NM_001127255.2(NLRP7):c.1104T>G (p.Ile368Met)	NLRP7 (I368M)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 893637	NM_001127255.2(NLRP7):c.930G>T (p.Gln310His)	NLRP7 (Q310H)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 97804	NM_001127255.2(NLRP7):c.574A>C (p.Met192Leu)	NLRP7 (M192L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 330181	NM_001127255.2(NLRP7):c.531C>T (p.His177=)	NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GConflicting classifications of pathogenicity

ClinVar