ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.37G>A (p.Asp13Asn)

dbSNP: rs1060502603
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000688790 SCV000816414 uncertain significance Fanconi anemia complementation group O 2022-09-19 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 568432). 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 (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. This variant has not been reported in the literature in individuals affected with RAD51C-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces aspartic acid, which is acidic and polar, with asparagine, which is neutral and polar, at codon 13 of the RAD51C protein (p.Asp13Asn).
Ambry Genetics RCV002352128 SCV002622258 uncertain significance Hereditary cancer-predisposing syndrome 2022-07-26 criteria provided, single submitter clinical testing The p.D13N variant (also known as c.37G>A), located in coding exon 1 of the RAD51C gene, results from a G to A substitution at nucleotide position 37. The aspartic acid at codon 13 is replaced by asparagine, an amino acid with highly 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.

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