ClinVar Miner

Submissions for variant NM_024529.4(CDC73):c.1236G>A (p.Met412Ile) (rs757006970)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000559332 SCV000636180 uncertain significance Parathyroid carcinoma 2018-09-05 criteria provided, single submitter clinical testing This sequence change replaces methionine with isoleucine at codon 412 of the CDC73 protein (p.Met412Ile). The methionine residue is moderately conserved and there is a small physicochemical difference between methionine and isoleucine. This variant is present in population databases (rs757006970, ExAC 0.006%). This variant has not been reported in the literature in individuals with CDC73-related disease. ClinVar contains an entry for this variant (Variation ID: 462742). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The isoleucine 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. 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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