ClinVar Miner

Submissions for variant NM_001130144.3(LTBP3):c.1846+6C>T

dbSNP: rs760385371
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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 RCV001950317 SCV002225517 uncertain significance Brachyolmia-amelogenesis imperfecta syndrome 2022-08-16 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. Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. ClinVar contains an entry for this variant (Variation ID: 1440089). This variant has not been reported in the literature in individuals affected with LTBP3-related conditions. This variant is present in population databases (rs760385371, gnomAD 0.003%). This sequence change falls in intron 12 of the LTBP3 gene. It does not directly change the encoded amino acid sequence of the LTBP3 protein. It affects a nucleotide within the consensus splice site.

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