Varaico: Literature-Extracted Genetic Variants

Gene:CFTR
Variant:p.S549R
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CFTR

NM_000492.4:p.S549R

Associated Papers

Profile of cystic fibrosis transmembrane conductance regulator (CFTR) gene variants across India and their variability in different geographic regions.

Chowdhury MR et al.

Gene, 2026

Long-term Outcomes of Pediatric CFSPID: A 15-Year Clinical and Genomic Study Across Newborn Screening Cystic Fibrosis Units.

Morales-Tirado A et al.

Archivos De Bronconeumologia, 2026

General trends in the calnexin-dependent expression and pharmacological rescue of clinical CFTR variants.

Tedman A et al.

Elife, 2025

41379933 (PubMed )
Supplement: elife-107180-supp1.xlsx › CANX_KO_Counts

Novel insight into CFTR gene's single nucleotide variants classification via in-silico analysis of a conserved site.

Rafique H et al.

Journal of Computer-aided Molecular Design, 2025

CFTR Modulator Response in Nasal Organoids Derived from People with Cystic Fibrosis.

Lo Cicero S et al.

Cells, 2025

Cystic fibrosis risk variants confer protection against inflammatory bowel disease.

Yu M et al.

Cell Genomics, 2025

41330381 (PubMed )
Supplement: mmc3.xlsx › Sheet1

Gene Editing for Cystic Fibrosis: Advances and Prospects of CRISPR-Cas9 Therapy.

Khurram I et al.

Cell Biology International, 2025

Characterization of Egyptian cystic fibrosis children including genotypes and phenotypes: A single tertiary center experience.

Fouda EM et al.

Respiratory Medicine, 2025

Efficacy of elexacaftor/tezacaftor/ivacaftor in non-cystic fibrosis bronchiectasis patients with a single pathogenic CFTR mutation: a retrospective cohort analysis.

Papadakis L et al.

Erj Open Research, 2025

41189580 (PubMed )
Supplement: 00007-2025.SUPPLEMENT.pdf

Genetically engineered approaches to the treatment of cystic fibrosis.

Safrygina AA et al.

Biophysical Reviews, 2025

General Trends in the Calnexin-Dependent Expression and Pharmacological Rescue of Clinical CFTR Variants.

Tedman A et al.

Biorxiv : the Preprint Server for Biology, 2025

40964320 (PubMed )
Supplement: media-1.pdf

Identification and Characterization of a Rare Exon 22 Duplication in CFTR in Two Families.

Ahting S et al.

International Journal of Molecular Sciences, 2025

40429633 (PubMed )
Supplement: ijms-26-04487-s001.zip › CFTR2_25September2024.xlsx › CFTR2_variants__genomic_info

Functional variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with increased risk of colorectal cancer.

Prizment A et al.

Human Molecular Genetics, 2025

39825500 (PubMed )
Supplement: supplementary_tables_ddaf007.xlsx › STable3

Genetic Variants and Clinical Characteristics in the Diagnosis of Children Aged Under 18 Years With Cystic Fibrosis in a Brazilian State.

Arpini LDSB et al.

Pediatric Pulmonology, 2025

Discovery and Development of CFTR Modulators for the Treatment of Cystic Fibrosis.

Wang X et al.

Journal of Medicinal Chemistry, 2025

Unraveling the Mechanism of Action, Binding Sites, and Therapeutic Advances of CFTR Modulators: A Narrative Review.

Baroni D

Current Issues in Molecular Biology, 2025

A new era of cystic fibrosis therapy with CFTR modulators.

Barros LGB et al.

Jornal Brasileiro De Pneumologia : Publicacao Oficial Da Sociedade Brasileira De Pneumologia E Tisilogia, 2025

Rescue of Mutant CFTR Channel Activity by Investigational Co-Potentiator Therapy.

Bacalhau M et al.

Biomedicines, 2025

Clinical impact of pharmacogenomics in pediatric care: insights extracted from clinical exome sequencing.

Maggo S et al.

Frontiers in Genetics, 2025

40510810 (PubMed )
Supplement: Table3.xlsx › Table_S1

Effect of CFTR modulators on glucose homeostasis in children and young adults with cystic fibrosis-related diabetes: a systematic review.

Giordano P et al.

Frontiers in Endocrinology, 2025

Pathogenic variation underlying rare diseases in an Arab population: Implications for screening programs.

Jain R et al.

Genetics in Medicine Open, 2025

A severe early presentation of cystic fibrosis in an infant with a homozygous c.1375_1383del CFTR variant- a case report.

Yousef A

Frontiers in Pediatrics, 2025

Highly Effective Modulator Therapy in Cystic Fibrosis: Addressing Unusual Variants in the Middle East.

Isse S et al.

Pulmonary Medicine, 2025

Cystic fibrosis risk variants confer protection against inflammatory bowel disease.

Yu M et al.

Medrxiv : the Preprint Server for Health Sciences, 2024

39677473 (PubMed )
Supplement: media-1.xlsx › ST3

Impact of the expanded label for elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with no F508del variant in the USA.

Cromwell EA et al.

The European Respiratory Journal, 2024

39227072 (PubMed )
Supplement: ERJ-01146-2024.Supplement.pdf

Impact of age at ivacaftor initiation on pulmonary outcomes among people with cystic fibrosis.

Merlo CA et al.

Thorax, 2024

Long-term impact of ivacaftor on mortality rate and health outcomes in people with cystic fibrosis.

Merlo CA et al.

Thorax, 2024

CFTR complex alleles and phenotypic variability in cystic fibrosis disease.

El-Seedy A et al.

Cellular and Molecular Biology (noisy-le-grand, France), 2024

Association between CFTR modulators and changes in iron deficiency markers in cystic fibrosis.

Jia S et al.

Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society, 2024

The clinical effectiveness of elexacaftor/tezacaftor/ivacaftor (ETI) for people with CF without a F508del variant: A systematic review and meta-analysis.

Lupas D et al.

Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society, 2024

Diagnosis of cystic fibrosis: a high heterogeneity of symptoms and genotypes in a Brazil population.

Meneses DG et al.

Bmc Pediatrics, 2024

Exploring the diversity of CFTR gene mutations in cystic fibrosis individuals of South Asia.

Rafique H et al.

The Journal of Asthma : Official Journal of the Association for the Care of Asthma, 2024

The Spectrum and Frequency of Cystic Fibrosis Mutations in Albanian Patients.

Kasmi I et al.

Balkan Journal of Medical Genetics : Bjmg, 2024

Distribution of pathogenic variants in the CFTR gene in a representative cohort of people with cystic fibrosis in the Kingdom of Bahrain.

Majed OAK et al.

Molecular Genetics and Genomics : Mgg, 2024

Contradiction in Star-Allele Nomenclature of Pharmacogenes between Common Haplotypes and Rare Variants.

Ahn SH et al.

Genes, 2024

38674455 (PubMed )
Supplement: genes-15-00521-s001.zip › Supplementary_Table.xls › Table_S1

Recommended Tool Compounds for Modifying the Cystic Fibrosis Transmembrane Conductance Regulator Channel Variants.

Han X et al.

Acs Pharmacology & Translational Science, 2024

Diagnosing Cystic Fibrosis in the 21st Century-A Complex and Challenging Task.

Anton-Păduraru DT et al.

Diagnostics (basel, Switzerland), 2024

Comparison of refugee patients with cystic fibrosis and their counterpart children from Turkey during the war.

Yılmaz Aİ et al.

European Journal of Pediatrics, 2024

Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences.

Ideozu JE et al.

Genome Medicine, 2024

38515211 (PubMed )
Supplement: 13073_2024_1316_MOESM1_ESM.xlsx › Table_S1B

Organic Synthesis and Current Understanding of the Mechanisms of CFTR Modulator Drugs Ivacaftor, Tezacaftor, and Elexacaftor.

Ferreira FC et al.

Molecules (basel, Switzerland), 2024

Benchmarking AlphaMissense Pathogenicity Predictions Against Cystic Fibrosis Variants.

McDonald EF et al.

Biorxiv : the Preprint Server for Biology, 2024

37873426 (PubMed )
Supplement: media-2.xlsx › Sheet1
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