ClinVar Miner

Submissions for variant NM_002185.5(IL7R):c.1232C>A (p.Thr411Lys)

dbSNP: rs1760216117
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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 RCV001212833 SCV001384432 uncertain significance Immunodeficiency 104 2019-09-27 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C25"). This variant has not been reported in the literature in individuals with IL7R-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces threonine with lysine at codon 411 of the IL7R protein (p.Thr411Lys). The threonine residue is highly conserved and there is a moderate physicochemical difference between threonine and lysine.

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