ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.4056_4065del (p.His1352fs)

dbSNP: rs1555095955
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000560088 SCV000622468 pathogenic Ataxia-telangiectasia syndrome 2023-12-17 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.His1352Glnfs*31) in the ATM gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in ATM are known to be pathogenic (PMID: 23807571, 25614872). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ATM-related conditions. ClinVar contains an entry for this variant (Variation ID: 453499). For these reasons, this variant has been classified as Pathogenic.
Ambry Genetics RCV002323895 SCV002631925 pathogenic Hereditary cancer-predisposing syndrome 2022-10-17 criteria provided, single submitter clinical testing The c.4056_4065del10 pathogenic mutation, located in coding exon 26 of the ATM gene, results from a deletion of 10 nucleotides at nucleotide positions 4056 to 4065, causing a translational frameshift with a predicted alternate stop codon (p.H1352Qfs*31). This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). This alteration is expected to result in loss of function by premature protein truncation or nonsense-mediated mRNA decay. As such, this alteration is interpreted as a disease-causing mutation.
Myriad Genetics, Inc. RCV004023642 SCV004930535 pathogenic Familial cancer of breast 2024-01-23 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

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