ClinVar Miner

Submissions for variant NM_001130144.3(LTBP3):c.3689_3692dup (p.Pro1232fs)

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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 RCV003592431 SCV004246828 uncertain significance Brachyolmia-amelogenesis imperfecta syndrome 2023-11-17 criteria provided, single submitter clinical testing This sequence change results in a frameshift in the LTBP3 gene (p.Pro1232Alafs*119). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 72 amino acid(s) of the LTBP3 protein and extend the protein by 46 additional amino acid residues. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with LTBP3-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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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