ClinVar Miner

Submissions for variant NM_002693.3(POLG):c.678G>C (p.Gln226His)

gnomAD frequency: 0.00052  dbSNP: rs147282197
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Total submissions: 18
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005396563 SCV006055463 uncertain significance Progressive sclerosing poliodystrophy; Mitochondrial DNA depletion syndrome 1; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1; Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis; Mitochondrial DNA depletion syndrome 4b 2022-05-17 criteria provided, single submitter research
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003317141 SCV004020890 uncertain significance not specified 2025-11-03 criteria provided, single submitter clinical testing Variant summary: POLG c.678G>C (p.Gln226His) results in a non-conservative amino acid change located in the DNA mitochondrial polymerase, exonuclease domain (IPR041336) of the encoded protein sequence. 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. The variant allele was found at a frequency of 0.00041 in 247722 control chromosomes, predominantly at a frequency of 0.00077 within the Non-Finnish European subpopulation in the gnomAD database. This frequency is not significantly higher than estimated for disease-causing variants in POLG, allowing no conclusion about variant significance. c.678G>C has been reported in the literature in individuals affected with POLG-Related Spectrum Disorders, including parkinsonism (Montaut_2018) and adult-onset chronic progressive external ophthalmoplegia (Heighton_2019) without strong evidence for causality, and as a compound heterozygous genotype together with a pathogenic variant in an individual diagnosed with sensory ataxic neuropathy with mtDNA deletions (Keller_2021). To our knowledge, no experimental evidence demonstrating an impact on protein function has been reported. The following publications have been ascertained in the context of this evaluation (PMID: 38871447, 31521625, 33600046, 29913018). ClinVar contains an entry for this variant (Variation ID: 206581). Based on the evidence outlined above, the variant was classified as uncertain significance.
Ambry Genetics RCV002362986 SCV002661810 uncertain significance Inborn genetic diseases 2024-12-11 criteria provided, single submitter clinical testing The c.678G>C (p.Q226H) alteration is located in exon 3 (coding exon 2) of the POLG gene. This alteration results from a G to C substitution at nucleotide position 678, causing the glutamine (Q) at amino acid position 226 to be replaced by a histidine (H). The p.Q226H alteration is predicted to be tolerated by in silico analysis. Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Mayo Clinic Laboratories, Mayo Clinic RCV000710188 SCV002541299 uncertain significance not provided 2025-06-26 criteria provided, single submitter clinical testing BP4, PM3
CENTOGENE GmbH and LLC - Guiding Precision Medicine RCV001808471 SCV002059496 uncertain significance Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 2019-06-05 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000710188 SCV001961537 uncertain significance not provided 2025-11-01 criteria provided, single submitter clinical testing POLG: PM2:Supporting, PM3:Supporting, BP4
Institute of Human Genetics, Cologne University RCV001263148 SCV001441226 uncertain significance Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 2024-01-30 criteria provided, single submitter research
Illumina Laboratory Services, Illumina RCV001121513 SCV001280138 uncertain significance POLG-related disorder 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine RCV000633538 SCV000887199 likely benign Progressive sclerosing poliodystrophy 2018-10-01 criteria provided, single submitter clinical testing The NM_002693.2:c.678G>C (NP_002684.1:p.Gln226His) [GRCH38: NC_000015.10:g.89330258C>G] variant in POLG gene is interpretated to be a Likely Benign based on ACMG guidelines (PMID: 25741868). This variant meets the following evidence codes reported in the ACMG-guideline. BS2:Observation of the variant in controls is inconsistent with penetrance of Mitochondrial DNA depletion syndrome 4A (Alpers type). BP4:Computational evidence/predictors indicate no impact on the POLG structure, function, or protein-protein interaction. Based on the evidence criteria codes applied, the variant is suggested to be Likely Benign.
Labcorp Genetics (formerly Invitae), Labcorp RCV000633538 SCV000754784 likely benign Progressive sclerosing poliodystrophy 2026-01-20 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000710188 SCV000709292 uncertain significance not provided 2018-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000710188 SCV000614733 uncertain significance not provided 2024-12-30 criteria provided, single submitter clinical testing Available data are insufficient to determine the clinical significance of the variant at this time. The frequency of this variant in the general population is uninformative in assessment of its pathogenicity. (http://gnomad.broadinstitute.org) Polyphen and MutationTaster yielded discordant predictions regarding whether this amino acid change is damaging to the protein.
GeneDx RCV000710188 SCV000242262 uncertain significance not provided 2025-06-10 criteria provided, single submitter clinical testing In silico analysis suggests that this missense variant does not alter protein structure/function; This variant is associated with the following publications: (PMID: 18156159, 21880868, 33600046, 40004527, 39595984)
PreventionGenetics, part of Exact Sciences RCV001121513 SCV005346115 uncertain significance POLG-related disorder 2024-07-05 no assertion criteria provided clinical testing The POLG c.678G>C variant is predicted to result in the amino acid substitution p.Gln226His. This variant has been reported in the compound heterozygous state in an individual with infantile muscular atrophy and weakness (Keller et al. 2021. PubMed ID: 33600046). Additionally, this variant was reported in the heterozygous state in one patient with clinical features suggestive of POLG deficiency, although a second plausible causative variant was not identified (Tang et al. 2011. PubMed ID: 21880868, Supplementary Table 3). This variant is reported in 0.076% of alleles in individuals of European (Non-Finnish) descent in gnomAD. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000710188 SCV001967299 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000710188 SCV001931330 likely benign not provided no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000710188 SCV001742578 likely benign not provided no assertion criteria provided clinical testing
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV000678826 SCV000805012 uncertain significance Autism; Seizure 2016-08-10 no assertion criteria provided clinical testing

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