C4014934[trait identifier] AND "Neuberg Centre For Genomic Medicine, N - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3235009	NM_181523.3(PIK3R1):c.1380_1397del (p.Ser460_Leu466delinsArg)	PIK3R1	Deletion (inframe_indel)	Immunodeficiency 36	GUncertain significance
Select item 2585209	NM_181523.3(PIK3R1):c.1628G>A (p.Arg543Lys)	PIK3R1 (R543K +3 more)	Single nucleotide variant (missense variant)	Immunodeficiency 36 +2 more	GUncertain significance