ClinVar Miner

Submissions for variant NM_001283009.2(RTEL1):c.3124C>T (p.Gln1042Ter)

dbSNP: rs929898540
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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 RCV001939342 SCV002237094 pathogenic Dyskeratosis congenita, autosomal recessive 5; Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3 2021-03-12 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln1042*) in the RTEL1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RTEL1 are known to be pathogenic (PMID: 23453664, 23959892, 25607374). This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with RTEL1-related conditions. For these reasons, this variant has been classified as Pathogenic.

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