List of variants reported as uncertain significance for immunodeficiency 14 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005026.5(PIK3CD):c.557C>T (p.Pro186Leu)	rs779715026	0.00002
NM_005026.5(PIK3CD):c.518C>A (p.Pro173His)	rs529803273	0.00001
NM_005026.5(PIK3CD):c.1243-7_1243-5del	rs746885189
NM_005026.5(PIK3CD):c.2780G>A (p.Arg927His)	rs2525160769

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