ClinVar Miner

Submissions for variant NM_001278293.3(ARL6):c.262C>T (p.Gln88Ter)

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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 RCV003028654 SCV003319618 pathogenic Bardet-Biedl syndrome 3; Retinitis pigmentosa 55 2022-02-23 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln88*) in the ARL6 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in ARL6 are known to be pathogenic (PMID: 15258860, 19858128, 20142850, 22334370, 27486776, 31736247). For these reasons, this variant has been classified as Pathogenic. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. This variant has not been reported in the literature in individuals affected with ARL6-related conditions. This variant is not present in population databases (gnomAD no frequency).

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