ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.1351A>G (p.Ser451Gly) (rs730881510)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000160037 SCV000210268 uncertain significance not provided 2014-01-06 criteria provided, single submitter clinical testing This variant is denoted BRCA2 c.1351A>G at the cDNA level, p.Ser451Gly (S451G) at the protein level, and results in the change of a Serine to a Glycine (AGC>GGC). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRCA2 Ser451Gly was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. This variant is a non-conservative substitution in which a neutral polar amino acid is replaced with a neutral non-polar one, altering a position that is only moderately conserved throughout evolution and is not located in a known functional domain (UniProt). In silico analyses predict this variant to have a benign effect on protein structure and function. Based on the currently available information, we consider BRCA2 Ser451Gly to be a variant of uncertain significance.

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