ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.266T>C (p.Ile89Thr)

gnomAD frequency: 0.00001  dbSNP: rs758974509
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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 RCV002002815 SCV002248190 uncertain significance Immunodeficiency 67 2022-06-03 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 (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. ClinVar contains an entry for this variant (Variation ID: 1472124). This variant has not been reported in the literature in individuals affected with IRAK4-related conditions. This variant is present in population databases (rs758974509, gnomAD 0.0009%). This sequence change replaces isoleucine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 89 of the IRAK4 protein (p.Ile89Thr).

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