ClinVar Miner

Submissions for variant NM_012472.6(DNAAF11):c.633C>A (p.Tyr211Ter)

dbSNP: rs750603177
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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 RCV000650322 SCV000772164 pathogenic Primary ciliary dyskinesia 19 2017-11-04 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Tyr211*) in the LRRC6 gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with LRRC6-related disease. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. Loss-of-function variants in LRRC6 are known to be pathogenic (PMID: 23122589). For these reasons, this variant has been classified as Pathogenic.

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