ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.6340_6341delinsCT (p.Gly2114Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005226107 SCV005864304 uncertain significance Marfan syndrome; Familial thoracic aortic aneurysm and aortic dissection 2024-12-18 criteria provided, single submitter clinical testing This sequence change replaces glycine, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 2114 of the FBN1 protein (p.Gly2114Leu). Information on the frequency of this variant in the gnomAD database is not available, as this variant may be reported differently in the database. This variant has not been reported in the literature in individuals affected with FBN1-related conditions. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be tolerated. 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.

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