ClinVar Miner

Submissions for variant NM_003119.3(SPG7):c.1553-?_1779+?del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000240505 SCV000299135 pathogenic Hereditary spastic paraplegia 7 2016-02-11 criteria provided, single submitter clinical testing This variant is an out-of-frame deletion of the genomic region encompassing exons 12-13 of the SPG7 gene. The precise impact of this deletion on mRNA splicing is unknown, however it is anticipated to result in a truncated protein product. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a SPG7-related disease. While this particular deletion has not been reported in the literature, loss of function variants in SPG7 are known to be pathogenic (PMID: 14985266, 9635427) and similar deletions have been reported in individuals affected with hereditary spastic paraplegia (PMID: 23065789, 22571692). For these reasons, this variant has been classified as Pathogenic.

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