ACMG/AMP 遗传性出血性远端血管扩张症基因-ENG 和 ACVRL1 的变异编辑指南规范

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-05-18 DOI:10.1155/2024/3043736
Desiree DeMille, Jamie McDonald, Carmelo Bernabeu, Hilary Racher, Carla Olivieri, Claudia Cantarini, Anna Sbalchiero, Bryony A. Thompson, Luca Jovine, Claire L. Shovlin, Sophie Dupuis-Girod, Gaetan Lesca, Maud Tusseau, Arupa Ganguly, Raj S. Kasthuri, Jaime Jessen, Maarten P. G. Massink, Shoji Ichikawa, Pinar Bayrak-Toydemir
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引用次数: 0

摘要

2015 年 ACMG/AMP 序列变异解读标准和指南已被实验室广泛使用,包括用于遗传性出血性毛细血管扩张症(HHT)基因的变异整理。然而,这些通用指南在发布之初就被认为需要针对特定基因和疾病进行修改和规范,以优化变异分类并使之标准化。为此,我们成立了 ClinGen HHT 变异整理专家小组。在此,我们介绍了我们推荐的 HHT 特异性变异体分类标准,以及对 ENG 和 ACVRL1 基因的 30 个变异体进行试点测试的结果。在最初的 ACMG/AMP 规则中,有 8 条被确定不适用于 ENG 或 ACVRL1 相关的 HHT,或之前 ClinGen 建议删除的规则,有 2 条规则未作修改,其余 18 条规则则根据 HHT 规范或之前 ClinGen 的一般建议进行了修改。这项研究表明了 HHT 特异性标准在优化和规范 HHT 变异分类以及解决分类冲突方面的重要性。
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Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1

The 2015 ACMG/AMP standards and guidelines for interpretation of sequence variants are widely used by laboratories, including for variant curation of the hereditary hemorrhagic telangiectasia (HHT) genes. However, the need for gene- and disease-specific modifications and specifications of these general guidelines to optimize and standardize variant classification was recognized at the time of publication. With this goal, the ClinGen HHT variant curation expert panel was formed. Here, we describe our recommended HHT-specific variant classification criteria and the outcomes from pilot testing of 30 variants of the ENG and ACVRL1 genes. Eight of the original ACMG/AMP rules were determined to not be applicable for ENG- or ACVRL1-related HHT or were previously recommended by ClinGen for removal, two rules were unmodified, and the remaining 18 rules were modified according to HHT specifications or previous ClinGen general recommendations. This study demonstrates the importance of HHT-specific criteria in the optimization and standardization of HHT variant classification and conflicting classification resolution.

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