ClinVar Miner

Submissions for variant NM_001371279.1(REEP1):c.792T>C (p.Pro264=)

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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 RCV005108336 SCV005728099 uncertain significance Hereditary spastic paraplegia 31 2024-02-02 criteria provided, single submitter clinical testing This sequence change disrupts the translational stop signal of the REEP1 mRNA. It is expected to extend the length of the REEP1 protein by 54 additional amino acid residues. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with REEP1-related conditions. This variant results in an extension of the REEP1 protein. Other variant(s) that result in a similarly extended protein product (p.*202Trpext*54) have been observed in individuals with REEP1-related disease (PMID: 29124833). This suggests that these extensions may be clinically significant. 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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