Varaico: Literature-Extracted Genetic Variants

Gene:RRAS
Variant:p.Q87L
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RRAS

NM_006270.5:p.Q87L

Associated Papers

Ras-Related Mutants Identified in Young-Onset Colorectal Cancer Display Divergent Phenotypes and Retain Their Pro-Angiogenic Effects.

David APL et al.

Cells, 2026

RRAS and RRAS2 mutations are recurrent oncogenic drivers in lung cancer and are sensitive to the pan-RAS inhibitor RMC-6236.

Pfeil AJ et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2026

RRAS and RRAS2 mutations are recurrent oncogenic drivers in lung cancer and are sensitive to the pan-RAS inhibitor RMC-6236.

Pfeil AJ et al.

Biorxiv : the Preprint Server for Biology, 2025

Mosaic RASopathies: A review of disorders caused by somatic pathogenic variants in the genes of the RAS/MAPK pathway.

Carli D et al.

American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2022

Genomic landscape of patients with FLT3-mutated acute myeloid leukemia (AML) treated within the CALGB 10603/RATIFY trial.

Jahn N et al.

Leukemia, 2022

35922444 (PubMed )
Supplement: 41375_2022_1650_MOESM2_ESM.xlsx › NGS_dataset

Genomic and Epigenomic Landscape of Juvenile Myelomonocytic Leukemia.

Fiñana C et al.

Cancers, 2022

The RASopathies: from pathogenetics to therapeutics.

Hebron KE et al.

Disease Models & Mechanisms, 2022

The RRAS2 pathogenic variant p.Q72L produces severe Noonan syndrome with hydrocephalus: A case report.

Weinstock NI et al.

American Journal of Medical Genetics. Part A, 2022

The acquisition of molecular drivers in pediatric therapy-related myeloid neoplasms.

Schwartz JR et al.

Nature Communications, 2021

33579957 (PubMed )
Supplement: 41467_2021_21255_MOESM24_ESM.xlsx › Sup._Data_21_Serial_Sequencing

Disease burden and conditioning regimens in ASCT1221, a randomized phase II trial in children with juvenile myelomonocytic leukemia: A Children's Oncology Group study.

Dvorak CC et al.

Pediatric Blood & Cancer, 2018

The genomic landscape of pediatric myelodysplastic syndromes.

Schwartz JR et al.

Nature Communications, 2017

An Oncogenic ALK Fusion and an RRAS Mutation in KRAS Mutation-Negative Pancreatic Ductal Adenocarcinoma.

Shimada Y et al.

The Oncologist, 2017

The genomic landscape of juvenile myelomonocytic leukemia.

Stieglitz E et al.

Nature Genetics, 2015

A short splicing isoform of afadin suppresses the cortical axon branching in a dominant-negative manner.

Umeda K et al.

Molecular Biology of the Cell, 2015

Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis.

Flex E et al.

Human Molecular Genetics, 2014

R-Ras controls axon branching through afadin in cortical neurons.

Iwasawa N et al.

Molecular Biology of the Cell, 2012

Semaphorin 4D/Plexin-B1 stimulates PTEN activity through R-Ras GTPase-activating protein activity, inducing growth cone collapse in hippocampal neurons.

Oinuma I et al.

The Journal of Biological Chemistry, 2010

Structure and function of the intracellular region of the plexin-b1 transmembrane receptor.

Tong Y et al.

The Journal of Biological Chemistry, 2009

The effector loop and prenylation site of R-Ras are involved in the regulation of integrin function.

Oertli B et al.

Oncogene, 2000

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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."