ClinVar Miner

Submissions for variant NM_000215.4(JAK3):c.81T>G (p.His27Gln)

gnomAD frequency: 0.00001  dbSNP: rs1039181282
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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 RCV002020094 SCV002290631 uncertain significance T-B+ severe combined immunodeficiency due to JAK3 deficiency 2021-08-31 criteria provided, single submitter clinical testing This sequence change replaces histidine with glutamine at codon 27 of the JAK3 protein (p.His27Gln). The histidine residue is weakly conserved and there is a small physicochemical difference between histidine and glutamine. This variant is not present in population databases (ExAC no frequency). This missense change has been observed in individual(s) with primary immunodeficiency (PMID: 29049190). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt JAK3 protein function. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a 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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