ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.2684A>C (p.Gln895Pro)

dbSNP: rs587781914
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001231012 SCV001403515 uncertain significance Hereditary breast ovarian cancer syndrome 2023-03-26 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. 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. ClinVar contains an entry for this variant (Variation ID: 957939). This variant has not been reported in the literature in individuals affected with BRCA1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glutamine, which is neutral and polar, with proline, which is neutral and non-polar, at codon 895 of the BRCA1 protein (p.Gln895Pro).
Ambry Genetics RCV002451544 SCV002739086 uncertain significance Hereditary cancer-predisposing syndrome 2021-09-02 criteria provided, single submitter clinical testing The p.Q895P variant (also known as c.2684A>C), located in coding exon 9 of the BRCA1 gene, results from an A to C substitution at nucleotide position 2684. The glutamine at codon 895 is replaced by proline, an amino acid with similar properties. This amino acid position is conserved. 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 RCV002451544 SCV003849428 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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