用于分析种系 ATM 序列变异的 ACMG/AMP 变异整理指南规范。

IF 8.1 1区 生物学 Q1 GENETICS & HEREDITY American journal of human genetics Pub Date : 2024-11-07 Epub Date: 2024-09-23 DOI:10.1016/j.ajhg.2024.08.022
Marcy E Richardson, Megan Holdren, Terra Brannan, Miguel de la Hoya, Amanda B Spurdle, Sean V Tavtigian, Colin C Young, Lauren Zec, Susan Hiraki, Michael J Anderson, Logan C Walker, Shannon McNulty, Clare Turnbull, Marc Tischkowitz, Katherine Schon, Thomas Slavin, William D Foulkes, Melissa Cline, Alvaro N Monteiro, Tina Pesaran, Fergus J Couch
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引用次数: 0

摘要

ClinGen 遗传性乳腺癌、卵巢癌和胰腺癌(HBOP)变异鉴定专家小组(VCEP)由国际公认的临床遗传学、分子生物学和变异解读专家组成。该 VCEP 根据 ClinGen 协议为美国医学遗传学会和分子病理学协会 (ACMG/AMP) 的共济失调毛细血管扩张症突变 (ATM) 基因指南制定了规范。这些针对 ATM 基因的特定规则是在 ACMG/AMP 指南的基础上修改而成的,并在试验性整理阶段对 33 个不同类型和分类的 ATM 变体进行了测试。试验结果表明,HBOP VCEP 分类与 ClinVar 中的分类大多一致。有 6 个试点变异在 ClinVar 中的解释存在冲突,根据 VCEP 的 ATM 特定规则重新评估后,有 4 个被 VCEP 归为良性变异,1 个可能是致病变异,1 个是意义不确定的变异 (VUS),从而提高了公共领域中解释的确定性。总体而言,33 个试点变异中有 28 个不属于 VUS,分类率达到 85%。ClinGen批准的修改后的规则证明了其在改进ATM变异解释方面的价值。
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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants.

The ClinGen Hereditary Breast, Ovarian, and Pancreatic Cancer (HBOP) Variant Curation Expert Panel (VCEP) is composed of internationally recognized experts in clinical genetics, molecular biology, and variant interpretation. This VCEP made specifications for the American College of Medical Genetics and Association for Molecular Pathology (ACMG/AMP) guidelines for the ataxia telangiectasia mutated (ATM) gene according to the ClinGen protocol. These gene-specific rules for ATM were modified from the ACMG/AMP guidelines and were tested against 33 ATM variants of various types and classifications in a pilot curation phase. The pilot revealed a majority agreement between the HBOP VCEP classifications and the ClinVar-deposited classifications. Six pilot variants had conflicting interpretations in ClinVar, and re-evaluation with the VCEP's ATM-specific rules resulted in four that were classified as benign, one as likely pathogenic, and one as a variant of uncertain significance (VUS) by the VCEP, improving the certainty of interpretations in the public domain. Overall, 28 of the 33 pilot variants were not VUS, leading to an 85% classification rate. The ClinGen-approved, modified rules demonstrated value for improved interpretation of variants in ATM.

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来源期刊
CiteScore
14.70
自引率
4.10%
发文量
185
审稿时长
1 months
期刊介绍: The American Journal of Human Genetics (AJHG) is a monthly journal published by Cell Press, chosen by The American Society of Human Genetics (ASHG) as its premier publication starting from January 2008. AJHG represents Cell Press's first society-owned journal, and both ASHG and Cell Press anticipate significant synergies between AJHG content and that of other Cell Press titles.
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