ClinVar Miner

Submissions for variant NM_000293.3(PHKB):c.530T>C (p.Leu177Pro)

dbSNP: rs770841932
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001048518 SCV001212529 uncertain significance Glycogen storage disease IXb 2022-06-26 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 845451). This variant has not been reported in the literature in individuals affected with PHKB-related conditions. This variant is present in population databases (rs770841932, gnomAD 0.0009%). This sequence change replaces leucine, which is neutral and non-polar, with proline, which is neutral and non-polar, at codon 177 of the PHKB protein (p.Leu177Pro).

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