ClinVar Miner

Submissions for variant NM_138773.4(SLC25A46):c.59A>T (p.Asp20Val)

dbSNP: rs1799533031
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001069579 SCV001234757 uncertain significance Neuropathy, hereditary motor and sensory, type 6B 2019-02-19 criteria provided, single submitter clinical testing This sequence change replaces aspartic acid with valine at codon 20 of the SLC25A46 protein (p.Asp20Val). The aspartic acid residue is moderately conserved and there is a large physicochemical difference between aspartic acid and valine. 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with SLC25A46-related conditions. This variant is not present in population databases (ExAC no frequency).

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