ClinVar Miner

Submissions for variant NM_000383.4(AIRE):c.872T>C (p.Leu291Pro)

gnomAD frequency: 0.00003  dbSNP: rs767272852
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001309246 SCV001498741 uncertain significance Polyglandular autoimmune syndrome, type 1 2021-09-01 criteria provided, single submitter clinical testing This sequence change replaces leucine with proline at codon 291 of the AIRE protein (p.Leu291Pro). The leucine residue is moderately conserved and there is a moderate physicochemical difference between leucine and proline. This variant is present in population databases (rs767272852, ExAC 0.02%). This variant has not been reported in the literature in individuals affected with AIRE-related conditions. 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 proline amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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.
Natera, Inc. RCV001309246 SCV002083880 uncertain significance Polyglandular autoimmune syndrome, type 1 2021-05-14 no assertion criteria provided clinical testing

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