"Blueprint Genetics"[submitter] AND "PIK3CD"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 636973	NM_005026.5(PIK3CD):c.323G>T (p.Arg108Leu)	PIK3CD (R108L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 636960	NM_005026.5(PIK3CD):c.397G>A (p.Asp133Asn)	PIK3CD (D133N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 636772	NM_005026.5(PIK3CD):c.460C>T (p.Arg154Trp)	PIK3CD (R154W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 581916	NM_005026.5(PIK3CD):c.1189G>A (p.Val397Met)	PIK3CD, LOC126805612 (V397M +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 582515	NM_005026.5(PIK3CD):c.1574A>G (p.Glu525Gly)	PIK3CD (E525G +2 more)	Single nucleotide variant (missense variant)	Immunodeficiency 14 +1 more	GConflicting classifications of pathogenicity
Select item 636918	NM_005026.5(PIK3CD):c.1690-3del	PIK3CD	Deletion (intron variant)	not provided	GUncertain significance
Select item 636715	NM_005026.5(PIK3CD):c.2389A>G (p.Met797Val)	PIK3CD (M797V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 88675	NM_005026.5(PIK3CD):c.3061G>A (p.Glu1021Lys)	PIK3CD (E1021K +2 more)	Single nucleotide variant (missense variant)	not provided +5 more	GPathogenic

ClinVar