ClinVar Miner

Submissions for variant NM_138773.4(SLC25A46):c.55C>A (p.Arg19=) (rs1186440654)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000703705 SCV000832619 uncertain significance Neuropathy, hereditary motor and sensory, type 6B 2018-05-17 criteria provided, single submitter clinical testing This sequence change affects codon 19 of the SLC25A46 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the SLC25A46 protein. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with SLC25A46-related disease. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. 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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