Special articleStandards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists
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Supported by the Association for Molecular Pathology.
Disclosures: E.J.D. is the Medical Director for Cofactor Genomics and claims ownership in P&V Licensing, LLC; A.Y. is a consultant for Foundation Medicine; A.M.T. received research funding from Foundation Medicine, EMD Serono, Baxalta, Bayer, and Onyx.
The Interpretation of Sequence Variants in Somatic Conditions Working Group is a working group of the Association for Molecular Pathology Clinical Practice Committee with liaison representation from the American College of Medical Genetics and Genomics (S.K. and D.J.W.), American Society of Clinical Oncology (A.M.T. and A.Y), and College of American Pathologists (M.D. and N.I.L.). The 2015 and 2016 Clinical Practice Committee consisted of Marina Nikiforova (Chair 2015 to 2016), Monica Basehore, Christopher Coldren, Linda Cook, Jennifer Crow, Birgit Funke, Meera Hameed, Larry Jennings, Arivarasan Karunamurthy, Annette Kim, Bryan Krock, Mary Lowery-Nordberg, Melissa Miller, Benjamin Pinsky, Somak Roy, Mark Routbort, Ryan Schmidt, and David Viswanatha.
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