ClinVar Miner

Submissions for variant NM_024753.5(TTC21B):c.3164G>A (p.Trp1055Ter)

dbSNP: rs772612775
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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 RCV002044728 SCV002110082 pathogenic Jeune thoracic dystrophy; Nephronophthisis 2021-04-11 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Trp1055*) in the TTC21B gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in TTC21B are known to be pathogenic (PMID: 18327258, 21068128, 21258341, 23559409, 24876116, 25492405, 27491411, 29068549). This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with TTC21B-related conditions. For these reasons, this variant has been classified as Pathogenic.

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