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. 2024 Jan 31;29:92. doi: 10.1186/s40001-024-01672-3

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 10 — Mutation differences between high- and low-risk patients in the TCGA cohort. A The waterfall plot shows mutation information for genes that were mutated in at least 3% of the samples in the high-risk group. B The waterfall plot shows mutation information for genes that were mutated in at least 3% of the samples in the low-risk group. Kaplan–Meier survival curves for the four patient groups stratified by risk score, TP53 mutation status (C), TTN mutation status (D), and SPOP mutation status (E)