ClinVar Miner

Submissions for variant NM_013335.4(GMPPA):c.250C>A (p.Gln84Lys)

gnomAD frequency: 0.00004  dbSNP: rs767718283
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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 RCV001892129 SCV002153790 uncertain significance Alacrima, achalasia, and intellectual disability syndrome 2024-10-21 criteria provided, single submitter clinical testing This sequence change replaces glutamine, which is neutral and polar, with lysine, which is basic and polar, at codon 84 of the GMPPA protein (p.Gln84Lys). This variant is present in population databases (rs767718283, gnomAD 0.006%). This variant has not been reported in the literature in individuals affected with GMPPA-related conditions. ClinVar contains an entry for this variant (Variation ID: 1379954). Invitae Evidence Modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) indicates that this missense variant is not expected to disrupt GMPPA protein function with a negative predictive value of 80%. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. 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.

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