ClinVar Miner

Submissions for variant NC_000011.9:g.(?_108217996)_(108218102_?)del

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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 RCV001379790 SCV001577656 likely pathogenic Ataxia-telangiectasia syndrome 2020-03-23 criteria provided, single submitter clinical testing This variant disrupts the kinase domain of the ATM protein, which is important for ATM's role in the DNA damage response (PMID: 23532176, 27097373, 28508083). While functional studies have not been performed to directly test the effect of this variant on ATM protein function, this suggests that disruption of this region of the protein is causative of disease. This variant has not been reported in the literature in individuals with ATM-related conditions. This variant is an in-frame deletion of the genomic region encompassing exon(s) 59 of the ATM gene. It preserves the integrity of the reading frame. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.

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