Varaico: Literature-Extracted Genetic Variants

Gene:RAC1
Variant:p.F28L
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RAC1

NM_006908.5:p.F28L

Associated Papers

New insights into the classification of the RAC1 P29S hotspot mutation in melanoma as an oncogene.

Mirzaiebadizi A et al.

Cancer Gene Therapy, 2025

Accurate affinity models for SH2 domains from peptide binding assays and free-energy regression.

Gagoski D et al.

Protein Science : a Publication of the Protein Society, 2025

41088778 (PubMed )
Supplement: PRO-34-e70317-s008.xlsx › _S6_-_PTMVar_-_Lyn

Accurate sequence-to-affinity models for SH2 domains from multi-round peptide binding assays coupled with free-energy regression.

Gagoski D et al.

Biorxiv : the Preprint Server for Biology, 2025

39764007 (PubMed )
Supplement: media-1.xlsx › _S6_-_PTMVar_-_Lyn

The mevalonate pathway contributes to breast primary tumorigenesis and lung metastasis.

Conde J et al.

Molecular Oncology, 2025

Tumor-derived RHOA mutants interact with effectors in the GDP-bound state.

Lin Y et al.

Nature Communications, 2024

Wavelet coherence phase analysis decodes the universal switching mechanism of Ras GTPase superfamily.

Motiwala Z et al.

Iscience, 2023

37448564 (PubMed )
Supplement: mmc2.xlsx › Sheet1

Molecular simulation unravels the amyloidogenic misfolding of nascent ApoA1 protein, driven by deleterious point mutations occurring in between 170-178 hotspot region.

Chandrasekhar G et al.

Journal of Biomolecular Structure & Dynamics, 2022

RAC1 Alterations Induce Acquired Dabrafenib Resistance in Association with Anaplastic Transformation in a Papillary Thyroid Cancer Patient.

Bagheri-Yarmand R et al.

Cancers, 2021

RAC1P29S is a spontaneously activating cancer-associated GTPase.

Davis MJ et al.

Proceedings of the National Academy of Sciences of the United States of America, 2013

Molecular dynamic simulation reveals damaging impact of RAC1 F28L mutation in the switch I region.

Kumar A et al.

Plos One, 2013

Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.

Krauthammer M et al.

Nature Genetics, 2012

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."