ClinVar Miner

Submissions for variant NM_000287.4(PEX6):c.1805del (p.Leu602fs)

dbSNP: rs2114242547
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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 RCV001389528 SCV001590920 pathogenic Peroxisome biogenesis disorder 2020-05-20 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in PEX6 are known to be pathogenic (PMID: 8670792, 19877282, 21031596). This variant has not been reported in the literature in individuals with PEX6-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Leu602Profs*17) in the PEX6 gene. It is expected to result in an absent or disrupted protein product.

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