ClinVar Miner

Submissions for variant NM_024685.4(BBS10):c.1447dup (p.Thr483fs)

dbSNP: rs759185809
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000673054 SCV000798220 likely pathogenic Bardet-Biedl syndrome 10 2018-03-01 criteria provided, single submitter clinical testing
Invitae RCV001388931 SCV001590085 pathogenic Bardet-Biedl syndrome 2023-10-29 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Thr483Asnfs*10) in the BBS10 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 241 amino acid(s) of the BBS10 protein. This variant is present in population databases (rs759185809, gnomAD 0.006%). This variant has not been reported in the literature in individuals affected with BBS10-related conditions. ClinVar contains an entry for this variant (Variation ID: 556979). This variant disrupts a region of the BBS10 protein in which other variant(s) (p.Val707*) have been determined to be pathogenic (PMID: 20472660, 22773737, 25982971, 27486776). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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