ClinVar Miner

Submissions for variant NM_000203.5(IDUA):c.246C>G (p.His82Gln)

gnomAD frequency: 0.00274  dbSNP: rs148775298
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Total submissions: 12
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000078387 SCV000110233 other not provided 2018-05-25 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000245681 SCV000302972 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000208604 SCV000627149 other Mucopolysaccharidosis type 1 2018-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000078387 SCV000730496 benign not provided 2018-09-28 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 27939258, 15300847, 23465405, 28721335, 33195954)
Counsyl RCV000664463 SCV000788427 other Hurler syndrome 2018-04-12 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000245681 SCV000919534 benign not specified 2017-12-20 criteria provided, single submitter clinical testing Variant summary: The IDUA c.246C>G (p.His82Gln) variant involves the alteration of a non-conserved nucleotide that is not located within a known functional domain (InterPro). 3/4 in silico tools predict a benign outcome for this variant (SNPsandGO not captured due to low reliability index). This variant was found in 766/261890 control chromosomes (gnomAD), including 2 homozygotes, at a frequency of 0.0029249, which is approximately equal to the estimated maximal expected allele frequency of a pathogenic IDUA variant (0.0026926). In addition, the frequency in the European (Non-Finnish) subpopulation, which includes the two homozygotes, is nearly 2 times higher than the estimated maximal allele frequency (0.00487), suggesting this variant may be a benign polymorphism. The variant has been identified in compound heterozygosity with other variants of possible pathogenicity in patients with an equivocal diagnosis of pseudodeficient MPS1, but patient clinical data and phase of the variants were not reported (Yogalingam_2004). In another published abstract, this variant was not found to segregate with disease in a MPS1 proband with 2 other causative mutation (Johnson_2007). The unaffected father and sister with severely reduced IDUA activity levels, were found to be obligate carriers who harbored this variant in compound heterozygosity with each of probands causative variants, thereby confirming the phase. The variant was found in the homozygous state via newborn screening where the enzyme activity level in a dried blood spot was borderline normal, suggesting the variant may be a pseudodeficiency allele (Scott_2013). A functional study in CHO cells suggests that while there is a reduction in enzyme activity using a fluorimetric substrate, the reduction would not be severe enough to be associated with a disease-causing mutation (Yogalingam_2004). Although the levels of enzyme activity when analyzed using a radiolabelled naturally derived disaccharide substrate were not reported in this study, all literature reports this variant as a pseudodeficiency allele. Another study showed a mild reduction in activity in leukocytes of a suspected MPS I patient with genotype c.246C>G/c.251G>C, but with normal urinary glycosaminoglycan (GAG) levels, suggesting the observed reduction in activity is not sufficient to impair GAG metabolism and cause disease (Bravo_2017). In addition, multiple clinical diagnostic laboratories/reputable databases have classified this variant as likely benign, benign, or as clinically benign but reported as a pseudodeficiency allele. Taken together, this variant is classified as Benign.
Mendelics RCV000664463 SCV001136675 likely benign Hurler syndrome 2019-05-28 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000208604 SCV001317786 uncertain significance Mucopolysaccharidosis type 1 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.
CeGaT Center for Human Genetics Tuebingen RCV000078387 SCV001748088 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing IDUA: BP4, BS2
Ambry Genetics RCV002453397 SCV002736213 likely benign Inborn genetic diseases 2017-12-28 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
GeneReviews RCV000208604 SCV000264373 not provided Mucopolysaccharidosis type 1 no assertion provided literature only Pseudodeficiency variants
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000078387 SCV001553224 likely benign not provided no assertion criteria provided clinical testing The IDUA p.His82Gln variant was identified in the literature in individuals with Mucopolysaccharidosis type I (MPS type I) disease (Bravo_2017_28721335, Clarke_2016_27939258,Yogalingam_2004_15300847). The variant was also identified in the following databases: dbSNP (ID: rs148775298) as “with other allele”, ClinVar (1x as benign by Gene Reviews, 1x as likely benign by Prevention Genetics, 1x as uncertain significance by EGL Genetic), Clinvitae (3x by ClinVar). This variant was identified in the 1000 Genomes Project in 6 of 5008 chromosomes (frequency: 0.0012), The NHLBI GO Exome Sequencing Project in 63 of 8578 European American alleles (freq. 0.007) and in 5 of 4383 of African American alleles (freq. 0.001), the Exome Aggregation Consortium database (August 8th 2016) in 293 (1 homozygous) of 80272 chromosomes (freq. 0.0036) and the genome Aggregation Database (beta, October 19th 2016) in 766 (2 homozygous) of 261890 chromosomes (freq. 0.003) in the following populations: African in 18 of 22820 chromosomes (freq. 0.0008), other in 16 of 6160 chromosomes (freq. 0.0025), Latino in 118 of 33784 chromosomes (freq. 0.003), European non Finnish in 569 of 116766 chromosomes (freq. 0.005), and Finnish in 45 of 24302 chromosomes (freq. 0.0018), but was not seen in Ashkenazi Jewish, East Asian and South Asian populations, increasing the likelihood this could be a low frequency variant. Lysosomal storage diseases (LSDs) are genetic disorders with an estimated overall prevalence of 1 in 7,700 live births. They are mainly caused by monogenic defects in genes encoding lysosomal enzymes that degrade macromolecules such as glycolipids, glycoproteins and mucopolysaccharides. These defects produce an abnormal and progressive lysosomal accumulation of specific substrates, leading to structural changes and deterioration of the cellular function. LSDs are clinically heterogeneous, being usually undetectable at birth, and characterized by progressive manifestations that may include different organs and systems in the body (Bravo_2017_28721335). A functional study on the level of protein synthesis, stability and specific activity of p.His82Gln variant has determined the nonpathogenic nature of this variant in a Mucopolysaccharidosis Type I patient (Yogalingam_2004_15300847). IDUA pseudodeficiency alleles can result in decreased enzyme activity when found in the homozygous state or in the compound heterozygous state with another pseudodeficiency allele, a pathogenic variant, or a variant of unknown significance. The Missouri NBS program reported that of 46 infants with a positive NBS screen, 26 had leukocyte IDUA enzyme activity below normal levels but above levels identified in patients with confirmed severe MPS I.36 Follow up testing showed that uGAG levels in these infants were not indicative of severe MPS I, and no patient was homozygous or compound heterozygous for previously reported pathogenic variants. Four purported pseudodeficiency missense IDUA alleles were identified (p.A79T, p.H82Q, p.D223N, and p.V322E) of which p.A79T was prevalent in the African American population (Clarke_2016_27939258). The p.His82Gln residue is not conserved in mammals and four out of five computational analyses (PolyPhen-2, SIFT, AlignGVGD, BLOSUM, MutationTaster) do not suggest a high likelihood of impact to the protein; however, this information is not predictive enough to rule out pathogenicity. The variant occurs outside of the splicing consensus sequence and 3 of 5 in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer, HumanSpliceFinder) predict a greater than 10% difference in splicing. However, this information is not predictive enough to assume pathogenicity. In summary, based on the above information, the clinical significance of this variant cannot be determined with certainty at this time although we would lean towards a more benign role for this variant. This variant is classified as likely benign.

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