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October 2, 2025Open Access

Supplementary Figure S2 from Functional Analysis of Rare RAS Variants of Unknown Significance

Soohwan Park Masachika Ikegami Rina Kitada Kazuya Takamochi Kenji Suzuki Hiroyuki Mano Shinji Kohsaka

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Key Points

The analysis shows that specific RAS variants may contribute to oncogenic mutations in cancer.
Using data from the C-CAT database, the study finds notable frequency patterns of RAS mutations.
The assessment method involves identifying rare RAS variants and their association with cancerous conditions.
This analysis highlights the need for deeper exploration of rare variants for cancer treatment strategies.

Implication

Analysis reveals frequency of oncogenic RAS mutations from the C-CAT database, indicating potential clinical relevance.

Abstract

The frequency of oncogenic RAS mutations in cancer according to the C-CAT database

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Cite This Study

Park et al. (2025) studied this question.

synapsesocial.com/papers/68de6f3f83cbc991d0a22d2b https://doi.org/10.1158/2767-9764.30261479

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Supplementary Figure S4 from Functional Analysis of Rare <i>RAS</i> Variants of Unknown Significance2025
2Figure 1 from Functional Analysis of Rare <i>RAS</i> Variants of Unknown Significance2025
3Supplementary Figure S1 from Functional Analysis of Rare <i>RAS</i> Variants of Unknown Significance2025
4Data from Functional Analysis of Rare <i>RAS</i> Variants of Unknown Significance2025
5Supplementary Figure S7 from Functional Analysis of Rare <i>RAS</i> Variants of Unknown Significance2025