ClinVar Miner

Submissions for variant NM_001999.4(FBN2):c.7796G>A (p.Cys2599Tyr)

dbSNP: rs1554116599
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002313343 SCV000739038 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2017-09-13 criteria provided, single submitter clinical testing The p.C2599Y variant (also known as c.7796G>A), located in coding exon 61 of the FBN2 gene, results from a G to A substitution at nucleotide position 7796. The cysteine at codon 2599 is replaced by tyrosine, an amino acid with highly dissimilar properties, and is located in a cbEGF-like domain. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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