ClinVar Miner

Submissions for variant NM_001256007.3(PNPLA8):c.1385G>A (p.Arg462Gln)

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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 RCV003121996 SCV003789212 uncertain significance not provided 2023-07-26 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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be tolerated. ClinVar contains an entry for this variant (Variation ID: 2420831). This variant has not been reported in the literature in individuals affected with PNPLA8-related conditions. This variant is present in population databases (rs557023667, gnomAD 0.006%). This sequence change replaces arginine, which is basic and polar, with glutamine, which is neutral and polar, at codon 462 of the PNPLA8 protein (p.Arg462Gln).

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