"Blueprint Genetics"[submitter] AND "PLCG2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 472893	NM_002661.5(PLCG2):c.1971G>C (p.Glu657Asp)	PLCG2 (E657D)	Single nucleotide variant (missense variant)	Familial cold autoinflammatory syndrome 3 +1 more	GUncertain significance
Select item 540095	NM_002661.5(PLCG2):c.2152A>G (p.Ser718Gly)	PLCG2 (S718G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 636889	NM_002661.5(PLCG2):c.2194C>T (p.Arg732Cys)	PLCG2 (R732C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 636653	NM_002661.5(PLCG2):c.2211C>A (p.Pro737=)	PLCG2	Single nucleotide variant (synonymous variant)	Familial cold autoinflammatory syndrome 3 +1 more	GUncertain significance
Select item 636970	NM_002661.5(PLCG2):c.2296A>C (p.Asn766His)	PLCG2 (N766H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 636525	NM_002661.5(PLCG2):c.2465A>C (p.Asn822Thr)	PLCG2 (N822T)	Single nucleotide variant (missense variant)	Familial cold autoinflammatory syndrome 3 +1 more	GUncertain significance

ClinVar