<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Behairy MY</submitter><funding>Taif University</funding><pubmed_abstract>The &lt;i>NRAS&lt;/i> gene is a well-known oncogene that acts as a major player in carcinogenesis. Mutations in the &lt;i>NRAS&lt;/i> gene have been linked to multiple types of human tumors. Therefore, the identification of the most deleterious single nucleotide polymorphisms (SNPs) in the &lt;i>NRAS&lt;/i> gene is necessary to understand the key factors of tumor pathogenesis and therapy. We aimed to retrieve &lt;i>NRAS&lt;/i> missense SNPs and analyze them comprehensively using sequence and structure approaches to determine the most deleterious SNPs that could increase the risk of carcinogenesis. We also adopted structural biology methods and docking tools to investigate the behavior of the filtered SNPs. After retrieving missense SNPs and analyzing them using six &lt;i>in silico&lt;/i> tools, 17 mutations were found </pubmed_abstract><journal>Frontiers in genetics</journal><pagination>872845</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9424727</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Computational Analysis of Deleterious SNPs in &lt;i>NRAS&lt;/i> to Assess Their Potential Correlation With Carcinogenesis.</pubmed_title><pmcid>PMC9424727</pmcid><pubmed_authors>Althobaiti F</pubmed_authors><pubmed_authors>Alaa Eldeen M</pubmed_authors><pubmed_authors>Behairy MY</pubmed_authors><pubmed_authors>Elfaky MA</pubmed_authors><pubmed_authors>Sileem AE</pubmed_authors><pubmed_authors>Darwish KM</pubmed_authors><pubmed_authors>Soltan MA</pubmed_authors><pubmed_authors>Ezz EM</pubmed_authors><pubmed_authors>Adam MS</pubmed_authors><pubmed_authors>Fayad E</pubmed_authors><pubmed_authors>Albogami S</pubmed_authors><pubmed_authors>Gouda AM</pubmed_authors><pubmed_authors>Refaat AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Computational Analysis of Deleterious SNPs in &lt;i>NRAS&lt;/i> to Assess Their Potential Correlation With Carcinogenesis.</name><description>The &lt;i>NRAS&lt;/i> gene is a well-known oncogene that acts as a major player in carcinogenesis. Mutations in the &lt;i>NRAS&lt;/i> gene have been linked to multiple types of human tumors. Therefore, the identification of the most deleterious single nucleotide polymorphisms (SNPs) in the &lt;i>NRAS&lt;/i> gene is necessary to understand the key factors of tumor pathogenesis and therapy. We aimed to retrieve &lt;i>NRAS&lt;/i> missense SNPs and analyze them comprehensively using sequence and structure approaches to determine the most deleterious SNPs that could increase the risk of carcinogenesis. We also adopted structural biology methods and docking tools to investigate the behavior of the filtered SNPs. After retrieving missense SNPs and analyzing them using six &lt;i>in silico&lt;/i> tools, 17 mutations were found </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-28T06:35:56.805Z</modification><creation>2024-11-07T00:35:15.752Z</creation></dates><accession>S-EPMC9424727</accession><cross_references><pubmed>36051694</pubmed><doi>10.3389/fgene.2022.872845</doi></cross_references></HashMap>