C3463897[trait identifier] AND "Diagnostic Laboratory, Department of G - 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 specified +1 more	GBenign
Select item 330158	NM_001127255.2(NLRP7):c.2682T>C (p.Tyr894=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1 +2 more	GBenign
Select item 287106	NM_001127255.2(NLRP7):c.1441G>A (p.Ala481Thr)	NLRP7 (A481T)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1 +1 more	GBenign
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 330183	NM_001127255.2(NLRP7):c.390G>A (p.Gln130=)	NLRP7	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 97894	NM_001127255.2(NLRP7):c.-39-16C>T	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole +1 more	GBenign

ClinVar