ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.7728T>C (p.Asn2576=) (rs1801188)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 10
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000080769 SCV000112671 benign not specified 2016-08-03 criteria provided, single submitter clinical testing
GeneDx RCV000080769 SCV000168142 benign not specified 2013-11-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000080769 SCV000268970 benign not specified 2014-10-29 criteria provided, single submitter clinical testing p.Asn2576Asn in exon 53 of DMD: This variant is not expected to have clinical si gnificance because it has been identified in 20% (1364/6728) of European America n chromosomes by the NHLBI Exome Sequencing Project ( u/EVS/; dbSNP rs1801188).
PreventionGenetics,PreventionGenetics RCV000080769 SCV000309943 benign not specified criteria provided, single submitter clinical testing
Ambry Genetics RCV000252250 SCV000317955 benign Cardiovascular phenotype 2015-06-29 criteria provided, single submitter clinical testing General population or subpopulation frequency is too high to be a pathogenic mutation based on disease/syndrome prevalence and penetrance
Illumina Clinical Services Laboratory,Illumina RCV000382472 SCV000482229 benign Dilated cardiomyopathy 3B 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000080769 SCV000603334 benign not specified 2018-07-06 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000576429 SCV000677278 benign Becker muscular dystrophy; Duchenne muscular dystrophy 2017-04-28 criteria provided, single submitter clinical testing
Phosphorus, Inc. RCV000578071 SCV000679894 benign Duchenne muscular dystrophy 2017-08-01 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000080769 SCV001364028 benign not specified 2019-02-18 criteria provided, single submitter clinical testing Variant summary: DMD c.7728T>C alters a non-conserved nucleotide resulting in a synonymous change. 5/5 computational tools predict no significant impact on normal splicing. However, these predictions have yet to be confirmed by functional studies. The variant allele was found at a frequency of 0.17 in 204704 control chromosomes, predominantly within the East Asian subpopulation at a frequency of 0.35 in the gnomAD database, including 584 homozygotes and 1751 hemizygotes. The observed variant frequency within East Asian control individuals in the gnomAD database is approximately 30 fold of the estimated maximal expected allele frequency for a pathogenic variant in DMD causing Dystrophinopathies phenotype (0.011), strongly suggesting that the variant is a benign polymorphism. To our knowledge, no occurrence of c.7728T>C in individuals affected with Dystrophinopathies and no experimental evidence demonstrating its impact on protein function have been reported. Six ClinVar submissions from clinical diagnostic laboratories (evaluation after 2014) cite the variant as likely benign/benign. Based on the evidence outlined above, the variant was classified as benign.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.