ClinVar Miner

Submissions for variant NM_003190.5(TAPBP):c.538_540dup (p.Leu180_Ser181insLeu)

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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 RCV005072358 SCV005700316 uncertain significance MHC class I deficiency 2024-07-23 criteria provided, single submitter clinical testing This variant, c.538_540dup, results in the insertion of 1 amino acid(s) of the TAPBP protein (p.Leu180dup), but otherwise preserves the integrity of the reading frame. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with TAPBP-related conditions. 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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