ClinVar Miner

Submissions for variant NM_019892.6(INPP5E):c.34G>C (p.Glu12Gln)

dbSNP: rs1835935570
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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 RCV001342986 SCV001536939 uncertain significance Familial aplasia of the vermis 2023-08-10 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. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) has been performed at Invitae for this missense variant, however the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on INPP5E protein function. ClinVar contains an entry for this variant (Variation ID: 1039501). This variant has not been reported in the literature in individuals affected with INPP5E-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glutamic acid, which is acidic and polar, with glutamine, which is neutral and polar, at codon 12 of the INPP5E protein (p.Glu12Gln).

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