ClinVar Miner

Submissions for variant NM_001044.5(SLC6A3):c.654-3C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002579252 SCV003489584 uncertain significance Parkinsonism-dystonia, infantile 2022-05-09 criteria provided, single submitter clinical testing This sequence change falls in intron 4 of the SLC6A3 gene. It does not directly change the encoded amino acid sequence of the SLC6A3 protein. It affects a nucleotide within the consensus splice site. This variant is present in population databases (rs764834876, gnomAD 0.2%). This variant has not been reported in the literature in individuals affected with SLC6A3-related conditions. 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 is not likely to affect RNA splicing. 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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