ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.640A>G (p.Ser214Gly)

gnomAD frequency: 0.00001  dbSNP: rs752144637
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000706981 SCV000836057 uncertain significance Mitochondrial complex II deficiency, nuclear type 1; Paragangliomas 5 2024-01-29 criteria provided, single submitter clinical testing This sequence change replaces serine, which is neutral and polar, with glycine, which is neutral and non-polar, at codon 214 of the SDHA protein (p.Ser214Gly). This variant is present in population databases (rs752144637, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with SDHA-related conditions. ClinVar contains an entry for this variant (Variation ID: 582812). 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 SDHA protein function with a negative predictive value of 95%. 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.
Ambry Genetics RCV002360833 SCV002661206 uncertain significance Hereditary cancer-predisposing syndrome 2022-02-27 criteria provided, single submitter clinical testing The p.S214G variant (also known as c.640A>G), located in coding exon 6 of the SDHA gene, results from an A to G substitution at nucleotide position 640. The serine at codon 214 is replaced by glycine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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