ClinVar Miner

Submissions for variant NM_006567.5(FARS2):c.28G>A (p.Ala10Thr)

dbSNP: rs753993545
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001879541 SCV002144499 uncertain significance Combined oxidative phosphorylation defect type 14 2021-08-15 criteria provided, single submitter clinical testing This sequence change replaces alanine with threonine at codon 10 of the FARS2 protein (p.Ala10Thr). The alanine residue is moderately conserved and there is a small physicochemical difference between alanine and threonine. This variant is present in population databases (rs753993545, ExAC 0.009%). This variant has not been reported in the literature in individuals affected with FARS2-related conditions. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt FARS2 protein function. 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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