ClinVar Miner

Submissions for variant NM_003849.4(SUCLG1):c.31A>G (p.Ile11Val)

gnomAD frequency: 0.00001  dbSNP: rs773513648
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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 RCV001977991 SCV002265248 uncertain significance Mitochondrial DNA depletion syndrome 9 2021-12-02 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. 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: "Not Available"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals affected with SUCLG1-related conditions. This variant is present in population databases (rs773513648, gnomAD 0.01%). This sequence change replaces isoleucine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 11 of the SUCLG1 protein (p.Ile11Val).

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