ClinVar Miner

Submissions for variant NM_002645.4(PIK3C2A):c.254A>G (p.Lys85Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002971614 SCV003282947 uncertain significance not provided 2022-07-12 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with PIK3C2A-related conditions. This variant is present in population databases (rs368452358, gnomAD 0.08%). This sequence change replaces lysine, which is basic and polar, with arginine, which is basic and polar, at codon 85 of the PIK3C2A protein (p.Lys85Arg).

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