ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.2608G>A (p.Ala870Thr)

dbSNP: rs753256448
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000687202 SCV000814756 uncertain significance Hereditary breast ovarian cancer syndrome 2023-08-02 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 567191). 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. 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 BRCA1 protein function. This variant has not been reported in the literature in individuals affected with BRCA1-related conditions. This variant is present in population databases (rs753256448, gnomAD 0.0009%). This sequence change replaces alanine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 870 of the BRCA1 protein (p.Ala870Thr).
Ambry Genetics RCV002440429 SCV002745533 uncertain significance Hereditary cancer-predisposing syndrome 2021-12-17 criteria provided, single submitter clinical testing The p.A870T variant (also known as c.2608G>A), located in coding exon 9 of the BRCA1 gene, results from a G to A substitution at nucleotide position 2608. The alanine at codon 870 is replaced by threonine, an amino acid with similar properties. This amino acid position is 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.
University of Washington Department of Laboratory Medicine, University of Washington RCV002440429 SCV003851042 likely benign Hereditary cancer-predisposing syndrome 2023-03-23 criteria provided, single submitter curation Missense variant in a coldspot region where missense variants are very unlikely to be pathogenic (PMID:31911673).

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