Varaico: Literature-Extracted Genetic Variants

Gene:ACE2
Variant:p.Q81*
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ACE2

NM_001371415.1:p.Q81*

Associated Papers

Combined mutations in nonstructural protein 14, envelope, and membrane proteins mitigate the neuropathogenicity of SARS-CoV-2 Omicron BA.1 in K18-hACE2 mice.

Sangare K et al.

Msphere, 2025

Evaluation of Genomic Surveillance of SARS-CoV-2 Virus Isolates and Comparison of Mutational Spectrum of Variants in Bangladesh.

Sultana A et al.

Viruses, 2025

Spike protein mutations and structural insights of pangolin lineage B.1.1.25 with implications for viral pathogenicity and ACE2 binding affinity.

Akter S et al.

Scientific Reports, 2023

Mutational dynamics across VOCs in International travellers and Community transmission underscores importance of Spike-ACE2 interaction.

Mehta P et al.

Microbiological Research, 2022

35779308 (PubMed )
Supplement: mmc1.xlsx › Supplementary_table_2

Phylogeography and genomic analysis of SARS-CoV-2 delta variant in Morocco.

El Mazouri S et al.

Journal of Infection in Developing Countries, 2022

The first three waves of the Covid-19 pandemic hint at a limited genetic repertoire for SARS-CoV-2.

Wassenaar TM et al.

Fems Microbiology Reviews, 2022

In-silico genomic landscape characterization and evolution of SARS-CoV-2 variants isolated in India shows significant drift with high frequency of mutations.

Ahmed-Abakur EH et al.

Saudi Journal of Biological Sciences, 2022

Genomic Characterization of SARS-CoV-2 Isolated from Patients with Distinct Disease Outcomes in Mexico.

Boukadida C et al.

Microbiology Spectrum, 2022

Genomic Diversity of SARS-CoV-2 in Algeria and North African Countries: What We Know So Far and What We Expect?

Menasria T et al.

Microorganisms, 2022

Molecular dynamic study of SARS-CoV-2 with various S protein mutations and their effect on thermodynamic properties.

Abdalla M et al.

Computers in Biology and Medicine, 2022

Two-step fitness selection for intra-host variations in SARS-CoV-2.

Li J et al.

Cell Reports, 2022

34982968 (PubMed )
Supplement: mmc3.pdf

Clinico-Genomic Analysis Reiterates Mild Symptoms Post-vaccination Breakthrough: Should We Focus on Low-Frequency Mutations?

Kanakan A et al.

Frontiers in Microbiology, 2022

Mapping Genetic Events of SARS-CoV-2 Variants.

Qin L et al.

Frontiers in Microbiology, 2022

Genomic landscape of alpha-variant of SARS-CoV-2 circulated in Pakistan.

Fiaz N et al.

Plos One, 2022

A next generation sequencing (NGS) analysis to reveal genomic and proteomic mutation landscapes of SARS-CoV-2 in South Asia.

Mahmood TB et al.

Current Research in Microbial Sciences, 2021

Phylogenomics and population genomics of SARS-CoV-2 in Mexico during the pre-vaccination stage reveals variants of interest B.1.1.28.4 and B.1.1.222 or B.1.1.519 and the nucleocapsid mutation S194L associated with symptoms.

Barona-Gómez F et al.

Microbial Genomics, 2021

Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant.

Liu Y et al.

Biorxiv : the Preprint Server for Biology, 2021

Molecular characterization of SARS-CoV-2 from Bangladesh: implications in genetic diversity, possible origin of the virus, and functional significance of the mutations.

Rahman MM et al.

Heliyon, 2021

Analysis of SARS-CoV-2 mutations in the United States suggests presence of four substrains and novel variants.

Wang R et al.

Communications Biology, 2021

33589648 (PubMed )
Supplement: 42003_2021_1754_MOESM1_ESM.pdf

Whole-genome sequencing of SARS-CoV-2 reveals the detection of G614 variant in Pakistan.

Umair M et al.

Plos One, 2021

Spike protein D614G and RdRp P323L: the SARS-CoV-2 mutations associated with severity of COVID-19.

Biswas SK et al.

Genomics & Informatics, 2020

Variant analysis of SARS-CoV-2 genomes.

Koyama T et al.

Bulletin of the World Health Organization, 2020

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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."