"Martin Pollak Laboratory, Beth Israel Deaconess Medical Center"[submi - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 64528	NM_001288772.2(PIK3C2G):c.1077A>T (p.Lys359Asn)	PIK3C2G (K359N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64529	NM_001288772.2(PIK3C2G):c.2714T>G (p.Leu905Arg)	PIK3C2G (L864R +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 64530	NM_001288772.2(PIK3C2G):c.2809A>T (p.Thr937Ser)	PIK3C2G (T896S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64531	NM_001288772.2(PIK3C2G):c.2918T>C (p.Val973Ala)	PIK3C2G (V932A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64532	NM_001288772.2(PIK3C2G):c.3459G>A (p.Leu1153=)	PIK3C2G	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 64533	NM_001288772.2(PIK3C2G):c.3816A>G (p.Glu1272=)	PIK3C2G	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 64534	NM_001288772.2(PIK3C2G):c.3822C>A (p.Ser1274Arg)	PIK3C2G (S1233R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar