ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.2164G>T (p.Ala722Ser)

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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 RCV002637491 SCV003514650 uncertain significance Myofibrillar myopathy 4 2022-10-13 criteria provided, single submitter clinical testing The LDB3 gene has multiple clinically relevant transcripts. This variant occurs in alternate transcript NM_007078.3, and corresponds to NM_001080116.1:c.*33582G>T in the primary transcript. This sequence change replaces alanine, which is neutral and non-polar, with serine, which is neutral and polar, at codon 722 of the LDB3 protein (p.Ala722Ser). 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with LDB3-related conditions. This variant is not present in population databases (gnomAD no frequency).

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