The American Journal of Human Genetics · 2024 · 16 citations · 61 references
MedicineGeneticsOncologyCancer GeneticsMedical GeneticsMolecular OncologyGermline Variant AnalysisGermline Variant InterpretationMutation AnalysisSomatic Variant InterpretationVariant ClassificationVariant InterpretationBenign Variant InterpretationClinical Variant CurationClinvar CurationHereditary Cancer Variant InterpretationLikely Pathogenic Variant InterpretationPathogenic Variant ClassificationSequence Variant CurationVariant Of Uncertain Significance Interpretation
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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