Varaico: Literature-Extracted Genetic Variants

Gene:ATP6AP1
Variant:p.G204R
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ATP6AP1

NM_001183.6:p.G204R

Associated Papers

Clinical characteristics and novel mutations of omicron subvariant XBB in Tamil Nadu, India - a cohort study.

Selvavinayagam ST et al.

The Lancet Regional Health. Southeast Asia, 2023

38076717 (PubMed )
Supplement: mmc1.pdf

An improved method for determining frequency of multiple variants of SARS-CoV-2 in wastewater using qPCR assays.

Fuzzen M et al.

The Science of the Total Environment, 2023

A Noncoding A-to-U Kozak Site Change Related to the High Transmissibility of Alpha, Delta, and Omicron VOCs.

Yang J et al.

Molecular Biology and Evolution, 2023

A comprehensive analysis of the mutational landscape of the newly emerging Omicron (B.1.1.529) variant and comparison of mutations with VOCs and VOIs.

Chakraborty C et al.

Geroscience, 2022

Comparative Analysis of SARS-CoV-2 Variants of Concern, Including Omicron, Highlights Their Common and Distinctive Amino Acid Substitution Patterns, Especially at the Spike ORF.

Nikolaidis M et al.

Viruses, 2022

Identification of a novel SARS-CoV-2 variant with a truncated protein in ORF8 gene by next generation sequencing.

DeRonde S et al.

Scientific Reports, 2022

Genomic surveillance, evolution and global transmission of SARS-CoV-2 during 2019-2022.

Sharif N et al.

Plos One, 2022

Evolution, Mode of Transmission, and Mutational Landscape of Newly Emerging SARS-CoV-2 Variants.

Chakraborty C et al.

Mbio, 2021

Characterizations of SARS-CoV-2 mutational profile, spike protein stability and viral transmission.

Laha S et al.

Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases, 2020

Comprehensive genomic variation profiling of cervical intraepithelial neoplasia and cervical cancer identifies potential targets for cervical cancer early warning.

Huang J et al.

Journal of Medical Genetics, 2019

30567904 (PubMed )
Supplement: jmedgenet-2018-105745supp001.pdf

Human phytanoyl-CoA hydroxylase: resolution of the gene structure and the molecular basis of Refsum's disease.

Jansen GA et al.

Human Molecular Genetics, 2000

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