<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(2)</volume><submitter>Suratekar R</submitter><pubmed_abstract>The highly contagious Delta variant of SARS-CoV-2 has become a prevalent strain globally and poses a public health challenge around the world. While there has been extensive focus on understanding the amino acid mutations in the Delta variant's Spike protein, the mutational landscape of the rest of the SARS-CoV-2 proteome (25 proteins) remains poorly understood. To this end, we performed a systematic analysis of mutations in all the SARS-CoV-2 proteins from nearly 2 million SARS-CoV-2 genomes from 176 countries/territories. Six highly prevalent missense mutations in the viral life cycle-associated Membrane (I82T), Nucleocapsid (R203M, D377Y), NS3 (S26L), and NS7a (V82A, T120I) proteins are almost exclusive to the Delta variant compared to other variants of concern (mean prevalence across g</pubmed_abstract><journal>Molecular systems biology</journal><pagination>e10673</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8842124</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High diversity in Delta variant across countries revealed by genome-wide analysis of SARS-CoV-2 beyond the Spike protein.</pubmed_title><pmcid>PMC8842124</pmcid><pubmed_authors>Soundararajan V</pubmed_authors><pubmed_authors>Donadio G</pubmed_authors><pubmed_authors>Ghosh P</pubmed_authors><pubmed_authors>Venkatakrishnan AJ</pubmed_authors><pubmed_authors>Suratekar R</pubmed_authors><pubmed_authors>Niesen MJM</pubmed_authors><pubmed_authors>Anand P</pubmed_authors></additional><is_claimable>false</is_claimable><name>High diversity in Delta variant across countries revealed by genome-wide analysis of SARS-CoV-2 beyond the Spike protein.</name><description>The highly contagious Delta variant of SARS-CoV-2 has become a prevalent strain globally and poses a public health challenge around the world. While there has been extensive focus on understanding the amino acid mutations in the Delta variant's Spike protein, the mutational landscape of the rest of the SARS-CoV-2 proteome (25 proteins) remains poorly understood. To this end, we performed a systematic analysis of mutations in all the SARS-CoV-2 proteins from nearly 2 million SARS-CoV-2 genomes from 176 countries/territories. Six highly prevalent missense mutations in the viral life cycle-associated Membrane (I82T), Nucleocapsid (R203M, D377Y), NS3 (S26L), and NS7a (V82A, T120I) proteins are almost exclusive to the Delta variant compared to other variants of concern (mean prevalence across g</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-05-31T02:02:14.577Z</modification><creation>2024-11-20T05:54:07.505Z</creation></dates><accession>S-EPMC8842124</accession><cross_references><pubmed>35156767</pubmed><doi>10.15252/msb.202110673</doi></cross_references></HashMap>