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. 2023 Aug 31;29(9):2295–2306. doi: 10.1038/s41591-023-02491-5

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© The Author(s) 2023

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 10 — (a) IGV screenshot of the pre- versus post-relapse CD138+ cells demonstrating that mutations in GPRC5D (structural variations, copy number variations, single nucleotide variations) were not detected prior to therapy. (b) Immunohistochemistry staining of CD138 and GPRC5D expression in the pre- versus post-relapse bone marrow biopsy samples.