Varaico: Literature-Extracted Genetic Variants

Gene:IFNAR1
Variant:p.V168L
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IFNAR1

NM_000629.3:p.V168L

Associated Papers

Impact of rare JAK/STAT germline mutations on vaccination-induced innate immune responses in a Tyrolian population.

Hennighausen L et al.

International Journal of Biological Sciences, 2026

Next-generation sequencing of CCR5, CXCR4, and IFNAR1 variants in relation to HIV-1 disease progression and ART response.

Pekkoc-Uyanik KC et al.

Scientific Reports, 2025

Association study of the JAK/STAT signaling pathway with susceptibility to COVID-19 in moroccan patient and in-silico analysis of rare variants.

El Houdi M et al.

Virus Research, 2025

Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.

Huang YC et al.

Journal of Personalized Medicine, 2023

Immunogenomic analysis of human brain metastases reveals diverse immune landscapes across genetically distinct tumors.

Álvarez-Prado ÁF et al.

Cell Reports. Medicine, 2023

36652909 (PubMed )
Supplement: mmc8.xlsx › BrM167

Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families.

Azzarà A et al.

Plos One, 2022

Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer.

Liu S et al.

Communications Biology, 2021

33907296 (PubMed )
Supplement: 42003_2021_2024_MOESM11_ESM.xlsx › Supplementary_Data_8

Genetic variability in COVID-19-related genes in the Brazilian population.

Secolin R et al.

Human Genome Variation, 2021

33824725 (PubMed )
Supplement: 41439_2021_146_MOESM3_ESM.xlsx › In_silico_prediction_results

Immune response genes receptors expression and polymorphisms in relation to multiple sclerosis susceptibility and response to INF-β therapy.

Karam RA et al.

Iubmb Life, 2016

TNFRSF10B polymorphisms and haplotypes associated with increased risk of death in non-small cell lung cancer.

Schabath MB et al.

Carcinogenesis, 2013

Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes.

Reyes-Gibby CC et al.

Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer, 2013

The role of non-HLA single nucleotide polymorphisms in multiple sclerosis susceptibility.

Bahreini SA et al.

Journal of Neuroimmunology, 2010

Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.

Hildebrandt MA et al.

Plos One, 2010

Role of inflammation gene polymorphisms on pain severity in lung cancer patients.

Reyes-Gibby CC et al.

Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2009

Recent advances in genetic analysis of multiple sclerosis: genetic associations and therapeutic implications.

Niino M et al.

Expert Review of Neurotherapeutics, 2007

Exhaustive genotyping of the interferon alpha receptor 1 (IFNAR1) gene and association of an IFNAR1 protein variant with AIDS progression or susceptibility to HIV-1 infection in a French AIDS cohort.

Diop G et al.

Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, 2006

IFNAR1 and IFNAR2 polymorphisms confer susceptibility to multiple sclerosis but not to interferon-beta treatment response.

Leyva L et al.

Journal of Neuroimmunology, 2005

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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."