"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "PIK3CD"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 753166	NM_005026.5(PIK3CD):c.449C>T (p.Ala150Val)	PIK3CD (A150V)	Single nucleotide variant (missense variant)	Immunodeficiency 14 +1 more	GConflicting classifications of pathogenicity
Select item 659165	NM_005026.5(PIK3CD):c.692C>T (p.Pro231Leu)	PIK3CD (P231L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 941354	NM_005026.5(PIK3CD):c.1459G>A (p.Ala487Thr)	LOC126805612, PIK3CD (A458T +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 14 +1 more	GConflicting classifications of pathogenicity
Select item 764550	NM_005026.5(PIK3CD):c.1726G>A (p.Val576Ile)	PIK3CD (V575I +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1162831	NM_005026.5(PIK3CD):c.2461C>T (p.Arg821Cys)	PIK3CD (R792C +2 more)	Single nucleotide variant (missense variant)	Immunodeficiency 14 +1 more	GUncertain significance
Select item 770679	NM_005026.5(PIK3CD):c.2873G>A (p.Gly958Asp)	PIK3CD (G929D +2 more)	Single nucleotide variant (missense variant)	Immunodeficiency 14 +1 more	GConflicting classifications of pathogenicity

ClinVar