ClinVar Miner

Submissions for variant NM_012448.4(STAT5B):c.417G>A (p.Gln139=)

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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 RCV003505888 SCV004259677 uncertain significance Growth hormone insensitivity with immune dysregulation 1, autosomal recessive 2023-12-31 criteria provided, single submitter clinical testing This sequence change affects codon 139 of the STAT5B mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the STAT5B protein. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with STAT5B-related conditions. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. 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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