ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.5897G>A (p.Ser1966Asn)

dbSNP: rs1555110520
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000584470 SCV000687650 uncertain significance Hereditary cancer-predisposing syndrome 2021-09-21 criteria provided, single submitter clinical testing This missense variant replaces serine with asparagine at codon 1966 of the ATM protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with hereditary cancer in the literature. This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.
Labcorp Genetics (formerly Invitae), Labcorp RCV000812625 SCV000952944 uncertain significance Ataxia-telangiectasia syndrome 2023-04-25 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available". The asparagine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. ClinVar contains an entry for this variant (Variation ID: 490628). This variant has not been reported in the literature in individuals affected with ATM-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces serine, which is neutral and polar, with asparagine, which is neutral and polar, at codon 1966 of the ATM protein (p.Ser1966Asn).
Ambry Genetics RCV000584470 SCV001186706 likely benign Hereditary cancer-predisposing syndrome 2022-06-22 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Sema4, Sema4 RCV000584470 SCV002537450 uncertain significance Hereditary cancer-predisposing syndrome 2021-09-29 criteria provided, single submitter curation
Natera, Inc. RCV000812625 SCV002075463 uncertain significance Ataxia-telangiectasia syndrome 2021-04-28 no assertion criteria provided clinical testing

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