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. Author manuscript; available in PMC: 2017 Dec 1.
Published in final edited form as: Cancer Discov. 2016 Oct 7;6(12):1342–1351. doi: 10.1158/2159-8290.CD-16-0607

Figure 2. Core, recurrent SNVs in HGSOC are restricted to TP53 mutations.

Figure 2

A) Oncoprint of all non-synonymous mutations in patient 539 reveals mutation of TP53 and distribution of mutations into core, shared, and private classes. B) A minority of SNVs and insertions/deletions (indels) are present in all samples (“core”). The majority of mutations are shared between 2–3 anatomic sites (“shared”), or present in only one site (“private”) C) Euler diagram of all non-synonymous SNVs and indels. Core SNVs/indels present in all anatomic sites are highlighted in red.