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. 2022 Nov 5;12:18813. doi: 10.1038/s41598-022-22879-6

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© The Author(s) 2022

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/.

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m7G-related gene mutations and CNV information in UCEC. (A) One hundred and fifty-two (28.73%) out of 529 patients show different genetic alterations. Of the missense mutation is the most common type of mutations. (B) 28 m7G-related gene copy number variants. (C) CNV change in location of intracellular m7G-related genes.