ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.796C>T (p.Pro266Ser)

gnomAD frequency: 0.00001  dbSNP: rs1418589091
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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 RCV001962289 SCV002136768 uncertain significance Fibrous dysplasia of jaw 2021-01-28 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. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C25". The serine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with SH3BP2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces proline with serine at codon 266 of the SH3BP2 protein (p.Pro266Ser). The proline residue is highly conserved and there is a moderate physicochemical difference between proline and serine.

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