{"title":"Clinical Interpretation of Sequence Variants","authors":"Junyu Zhang, Yanyi Yao, Haixian He, Jun Shen","doi":"10.1002/cphg.98","DOIUrl":null,"url":null,"abstract":"<p>Clinical interpretation of DNA sequence variants is a critical step in reporting clinical genetic testing results. Application of next-generation sequencing technology in molecular genetic testing has facilitated diagnoses of genetic disorders in clinical practice. However, the large number of DNA sequence variants detected in clinical specimens, many of which have never been seen before, make clinical interpretation challenging. Recommendations by the American College of Medical Genetics and Genomics and the Association for Molecular Pathology (ACMG/AMP) have been widely adopted by clinical laboratories around the world to guide clinical interpretation of sequence variants. The ClinGen Sequence Variant Interpretation Working Group and various disease-specific variant curation expert panels have also developed specifications for the ACMG/AMP recommendations. Despite these efforts to standardize variant interpretation in clinical practice, different laboratories may subjectively use professional judgment to determine which criteria are applicable when classifying a variant. In addition, clinicians and researchers who are not familiar with the variant interpretation process may have difficulty understanding clinical genetic reports and communicating the clinical significance of genetic testing results. Here we provide a step-by-step protocol for clinical interpretation of sequence variants, including practical examples. By following this protocol, clinical laboratory geneticists can interpret the clinical significance of sequence variants according to the ACMG/AMP recommendations and ClinGen framework. Furthermore, this article will help clinicians and researchers to understand variant classification in clinical genetic testing reports and evaluate the quality of the reports. © 2020 by John Wiley & Sons, Inc.</p><p><b>Basic Protocol</b>: Interpreting the clinical significance of sequence variants</p><p><b>Support Protocol</b>: Reevaluating the clinical significance of sequence variants</p>","PeriodicalId":40007,"journal":{"name":"Current Protocols in Human Genetics","volume":"106 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cphg.98","citationCount":"40","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Human Genetics","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cphg.98","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 40
Abstract
Clinical interpretation of DNA sequence variants is a critical step in reporting clinical genetic testing results. Application of next-generation sequencing technology in molecular genetic testing has facilitated diagnoses of genetic disorders in clinical practice. However, the large number of DNA sequence variants detected in clinical specimens, many of which have never been seen before, make clinical interpretation challenging. Recommendations by the American College of Medical Genetics and Genomics and the Association for Molecular Pathology (ACMG/AMP) have been widely adopted by clinical laboratories around the world to guide clinical interpretation of sequence variants. The ClinGen Sequence Variant Interpretation Working Group and various disease-specific variant curation expert panels have also developed specifications for the ACMG/AMP recommendations. Despite these efforts to standardize variant interpretation in clinical practice, different laboratories may subjectively use professional judgment to determine which criteria are applicable when classifying a variant. In addition, clinicians and researchers who are not familiar with the variant interpretation process may have difficulty understanding clinical genetic reports and communicating the clinical significance of genetic testing results. Here we provide a step-by-step protocol for clinical interpretation of sequence variants, including practical examples. By following this protocol, clinical laboratory geneticists can interpret the clinical significance of sequence variants according to the ACMG/AMP recommendations and ClinGen framework. Furthermore, this article will help clinicians and researchers to understand variant classification in clinical genetic testing reports and evaluate the quality of the reports. © 2020 by John Wiley & Sons, Inc.
Basic Protocol: Interpreting the clinical significance of sequence variants
Support Protocol: Reevaluating the clinical significance of sequence variants
序列变异的临床解释。
DNA序列变异的临床解释是报告临床基因检测结果的关键一步。下一代测序技术在分子遗传检测中的应用促进了临床实践中遗传疾病的诊断。然而,在临床标本中检测到的大量DNA序列变异,其中许多以前从未见过,这使得临床解释具有挑战性。美国医学遗传学与基因组学学院和分子病理学协会(ACMG/AMP)的建议已被世界各地的临床实验室广泛采用,以指导序列变异的临床解释。ClinGen序列变异解释工作组和各种疾病特异性变异管理专家小组也为ACMG/AMP建议制定了规范。尽管在临床实践中努力将变体解释标准化,但不同的实验室可能会主观地使用专业判断来确定在对变体进行分类时适用哪些标准。此外,不熟悉变体解释过程的临床医生和研究人员可能难以理解临床基因报告并传达基因检测结果的临床意义。在这里,我们提供了一个逐步的方案,用于序列变异的临床解释,包括实际的例子。通过遵循该方案,临床实验室遗传学家可以根据ACMG/AMP建议和ClinGen框架来解释序列变异的临床意义。此外,本文将帮助临床医生和研究人员了解临床基因检测报告中的变异分类,并评估报告的质量。©2020 John Wiley&Sons,股份有限公司基本方案:解释序列变异的临床意义支持方案:重新评估序列变异的医学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。