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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants.

Authors :
Richardson, Marcy E.
Holdren, Megan
Brannan, Terra
de la Hoya, Miguel
Spurdle, Amanda B.
Tavtigian, Sean V.
Young, Colin C.
Zec, Lauren
Hiraki, Susan
Anderson, Michael J.
Walker, Logan C.
McNulty, Shannon
Turnbull, Clare
Tischkowitz, Marc
Schon, Katherine
Slavin, Thomas
Foulkes, William D.
Cline, Melissa
Monteiro, Alvaro N.
Pesaran, Tina
Source :
American Journal of Human Genetics. Nov2024, Vol. 111 Issue 11, p2411-2426. 16p.
Publication Year :
2024

Abstract

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. This paper details ACMG/AMP-style guidelines for ataxia telangiectasia mutated (ATM) variant interpretation and shows the results of pilot classifications. Several phenotype-driven rules were omitted or modified due to low-penetrance and commonness of breast cancer. This work aims to harmonize the classification of ATM variants and avoid misinterpretation by using standard rules. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00029297
Volume :
111
Issue :
11
Database :
Academic Search Index
Journal :
American Journal of Human Genetics
Publication Type :
Academic Journal
Accession number :
180678033
Full Text :
https://doi.org/10.1016/j.ajhg.2024.08.022