ClinVar Miner

Submissions for variant NM_003119.4(SPG7):c.861T>C (p.Phe287=)

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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 RCV003618903 SCV004526617 uncertain significance Hereditary spastic paraplegia 7 2023-12-22 criteria provided, single submitter clinical testing This sequence change affects codon 287 of the SPG7 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the SPG7 protein. It affects a nucleotide within the consensus splice site. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with SPG7-related conditions. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing. 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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