ClinVar Miner

Submissions for variant NM_012448.4(STAT5B):c.1030A>C (p.Thr344Pro)

dbSNP: rs1598302816
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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 RCV001218212 SCV001390084 uncertain significance Growth hormone insensitivity with immune dysregulation 1, autosomal recessive 2019-06-12 criteria provided, single submitter clinical testing This sequence change replaces threonine with proline at codon 344 of the STAT5B protein (p.Thr344Pro). The threonine residue is highly conserved and there is a small physicochemical difference between threonine and proline. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with STAT5B-related conditions. 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: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C35"). 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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