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Published in: Familial Cancer 2/2016

01-04-2016 | Short Communication

Germline BAP1 mutations misreported as somatic based on tumor-only testing

Authors: Mohamed H. Abdel-Rahman, Karan Rai, Robert Pilarski, Frederick H. Davidorf, Colleen M. Cebulla

Published in: Familial Cancer | Issue 2/2016

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Abstract

We present three unrelated patients with germline mutations in BAP1 misreported as somatic mutations. All had strong family histories of cancer. One of these patients presented with an invasive breast cancer with the tumor tissue showing partial loss of the mutant rather than the wild type allele, suggesting that the germline BAP1 mutation didn’t contribute to breast cancer development in this patient. This data highlights the importance of sequencing matching germline and tumor DNA for proper assessment of somatic versus germline mutation status. In patients with somatic mutations reported from laboratories carrying out tumor-only genomic testing, the possibility that a variant may be a germline mutation should be considered, especially if the personal and/or family history suggests hereditary cancer predisposition. Since tumor-only testing can reveal germline mutations, ethical issues for patients being tested should be considered including proper consent and genetic counseling.
Literature
9.
go back to reference Rai K, Pilarski R, Cebulla CM, Abdel-Rahman MH (2015) Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases. Clin Genet. doi:10.1111/cge.12630 PubMed Rai K, Pilarski R, Cebulla CM, Abdel-Rahman MH (2015) Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases. Clin Genet. doi:10.​1111/​cge.​12630 PubMed
Metadata
Title
Germline BAP1 mutations misreported as somatic based on tumor-only testing
Authors
Mohamed H. Abdel-Rahman
Karan Rai
Robert Pilarski
Frederick H. Davidorf
Colleen M. Cebulla
Publication date
01-04-2016
Publisher
Springer Netherlands
Published in
Familial Cancer / Issue 2/2016
Print ISSN: 1389-9600
Electronic ISSN: 1573-7292
DOI
https://doi.org/10.1007/s10689-016-9865-9

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