Varaico: Literature-Extracted Genetic Variants

Gene:KRAS
Variant:p.N116S
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KRAS

NM_004985.5:p.N116S

Associated Papers

The role of MLH1, MSH2 and MSH6 in the development of colorectal cancer in Uganda.

Wismayer R et al.

Bmc Cancer, 2025

Comprehensive structure-function analysis reveals gain- and loss-of-function mechanisms impacting oncogenic KRAS activity.

Kwon JJ et al.

Biorxiv : the Preprint Server for Biology, 2024

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.

Ahram DF et al.

Journal of the American Society of Nephrology : Jasn, 2023

KRAS and RAS-MAPK Pathway Deregulation in Mature B Cell Lymphoproliferative Disorders.

Vendramini E et al.

Cancers, 2022

Clinical and Functional Characterization of Atypical KRAS/NRAS Mutations in Metastatic Colorectal Cancer.

Loree JM et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2021

Structural bioinformatics enhances mechanistic interpretation of genomic variation, demonstrated through the analyses of 935 distinct RAS family mutations.

Tripathi S et al.

Bioinformatics (oxford, England), 2021

33226070 (PubMed )
Supplement: btaa972_supplementary_data.zip › RAS_Manuscript_RMarkdown.tar.gz › RAS_Manuscript1.Revised › RAS_Variants_Scores.xlsx › Sheet1

Swimming toward solutions: Using fish and frogs as models for understanding RASopathies.

Patterson VL et al.

Birth Defects Research, 2020

Craniofacial, orofacial and dental disorders: the role of the RAS/ERK pathway.

Vogiatzi A et al.

Expert Reviews in Molecular Medicine, 2019

Somatic alterations in circulating cell-free DNA of oesophageal carcinoma patients during primary staging are indicative for post-surgical tumour recurrence.

Pasternack H et al.

Scientific Reports, 2018

The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK Pathway.

Tajan M et al.

Endocrine Reviews, 2018

K-Ras(V14I) -induced Noonan syndrome predisposes to tumour development in mice.

Hernández-Porras I et al.

The Journal of Pathology, 2016

Characterization of a novel KRAS mutation identified in Noonan syndrome.

Razzaque MA et al.

American Journal of Medical Genetics. Part A, 2012

Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back.

Rauen KA et al.

American Journal of Medical Genetics. Part A, 2010

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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."