Erratum: Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC) (Genetics in Medicine (2022) 24(5) (986–998), (S1098360022000016), (10.1016/j.gim.2022.01.001))

Peter Horak, Malachi Griffith, Arpad M. Danos, Beth A. Pitel, Subha Madhavan, Xuelu Liu, Cynthia Chow, Heather Williams, Leigh Carmody, Lisa Barrow-Laing, Damian Rieke, Simon Kreutzfeldt, Albrecht Stenzinger, David Tamborero, Manuela Benary, Padma Sheila Rajagopal, Cristiane M. Ida, Harry Lesmana, Laveniya Satgunaseelan, Jason D. MerkerMichael Y. Tolstorukov, Paulo Vidal Campregher, Jeremy L. Warner, Shruti Rao, Maya Natesan, Haolin Shen, Jeffrey Venstrom, Somak Roy, Kayoko Tao, Rashmi Kanagal-Shamanna, Xinjie Xu, Deborah I. Ritter, Kym Pagel, Kilannin Krysiak, Adrian Dubuc, Yassmine M. Akkari, Xuan Shirley Li, Jennifer Lee, Ian King, Gordana Raca, Alex Wagner, Marylin M. Li, Sharon E. Plon, Shashikant Kulkarni, Obi L. Griffith, Debyani Chakravarty, Dmitriy Sonkin

Research output: Contribution to journalComment/debate

5 Scopus citations

Abstract

Correction to: Genetics in Medicine 2022; https://doi.org/10.1016/j.gim.2022.01.001 In the article “Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)” by Horak et al (Genet Med 2022;24:986-998), there were 3 errors in Table 2 where the terms OM3 and OM4 were used incorrectly. The article has been corrected online and can be accessed at https://doi.org/10.1016/j.gim.2022.01.001.

Original languageEnglish
Pages (from-to)1991
Number of pages1
JournalGenetics in Medicine
Volume24
Issue number9
DOIs
StatePublished - Sep 2022

Fingerprint

Dive into the research topics of 'Erratum: Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC) (Genetics in Medicine (2022) 24(5) (986–998), (S1098360022000016), (10.1016/j.gim.2022.01.001))'. Together they form a unique fingerprint.

Cite this