Total submissions: 3
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Ambry Genetics | RCV001015792 | SCV001176667 | uncertain significance | Hereditary cancer-predisposing syndrome | 2022-02-11 | criteria provided, single submitter | clinical testing | The p.N845H variant (also known as c.2533A>C), located in coding exon 16 of the ATM gene, results from an A to C substitution at nucleotide position 2533. The asparagine at codon 845 is replaced by histidine, an amino acid with similar properties. This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. |
| Invitae | RCV001054377 | SCV001218688 | uncertain significance | Ataxia-telangiectasia syndrome | 2022-01-26 | criteria provided, single submitter | clinical testing | This sequence change replaces asparagine, which is neutral and polar, with histidine, which is basic and polar, at codon 845 of the ATM protein (p.Asn845His). 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: 821407). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt ATM protein function. 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. |
| Mendelics | RCV002249632 | SCV002516945 | uncertain significance | not specified | 2022-05-04 | criteria provided, single submitter | clinical testing |