Varaico: Literature-Extracted Genetic Variants

Gene:KRAS
Variant:p.V152A
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KRAS

NM_004985.5:p.V152A

Associated Papers

Finding driver mutations in cancer: Elucidating the role of background mutational processes.

Brown AL et al.

Plos Computational Biology, 2019

31034466 (PubMed )
Supplement: pcbi.1006981.s010.xlsx › final_benchmark

Clinical and molecular aspects of RAS related disorders.

Denayer E et al.

Journal of Medical Genetics, 2008

Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction.

Gelb BD et al.

Human Molecular Genetics, 2006

Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype.

Carta C et al.

American Journal of Human Genetics, 2006

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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."