ClinVar Miner

Submissions for variant NM_001379200.1(TBX1):c.1152_1160dup (p.Gly390_Leu391insAlaGlyGly)

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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 RCV003105676 SCV003793388 uncertain significance DiGeorge syndrome 2022-09-19 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. This variant has not been reported in the literature in individuals affected with TBX1-related conditions. This variant, c.1125_1133dup, results in the insertion of 3 amino acid(s) of the TBX1 protein (p.Ala379_Gly381dup), but otherwise preserves the integrity of the reading frame. This variant is not present in population databases (gnomAD no frequency).

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