Varaico: Literature-Extracted Genetic Variants

Gene:TFRC
Variant:p.G142S
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TFRC

NM_001128148.3:p.G142S

Associated Papers

Germline Variants in the Immune Response-Related Genes: Possible Modifying Effect on Age-Dependent BRCA1 Penetrance in Breast Cancer Patient.

Kuligina ES et al.

Cancers, 2025

41374957 (PubMed )
Supplement: cancers-17-03756-s001.zip › Table_S4a.xlsx › Table_S4a

Proteogenomic Profiling of Treatment-Naïve Metastatic Malignant Melanoma.

Kuras M et al.

Cancers, 2025

40075679 (PubMed )
Supplement: cancers-17-00832-s001.zip › Table_S5._SAAVs.xlsx › Table_S5A

Translational and clinical comparison of whole genome and transcriptome to panel sequencing in precision oncology.

Kerle IA et al.

Npj Precision Oncology, 2025

39794422 (PubMed )
Supplement: 41698_2024_788_MOESM7_ESM.xlsx › patient_10_panel_small_variants

Combining germline, tissue and liquid biopsy analysis by comprehensive genomic profiling to improve the yield of actionable variants in a real-world cancer cohort.

Vanni I et al.

Journal of Translational Medicine, 2024

38750555 (PubMed )
Supplement: 12967_2024_5227_MOESM15_ESM.xlsx › S15

Comprehensive Genomic and Transcriptomic Analysis of Three Synchronous Primary Tumours and a Recurrence from a Head and Neck Cancer Patient.

Bresadola L et al.

International Journal of Molecular Sciences, 2021

34299215 (PubMed )
Supplement: ijms-22-07583-s001.zip › SupplementaryTable3.xlsx › germline_mutations

A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.

Bell S et al.

Communications Biology, 2021

33536631 (PubMed )
Supplement: 42003_2020_1575_MOESM4_ESM.xlsx › Supplementary_Data_2

Quality control of single amino acid variations detected by tandem mass spectrometry.

Yi X et al.

Journal of Proteomics, 2018

Birth Characteristics and Childhood Leukemia Risk: Correlations With Genetic Markers.

Kennedy AE et al.

Journal of Pediatric Hematology/oncology, 2015

Transferrin receptor levels and polymorphism of its gene in age-related macular degeneration.

Wysokinski D et al.

Acta Biochimica Polonica, 2015

The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.

Tang X et al.

Nucleic Acids Research, 2014

25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A0EM-01A.domain

Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Szeto CY et al.

Febs Open Bio, 2014

24490137 (PubMed )
Supplement: mmc5.xlsx › coding

A bioinformatics workflow for variant peptide detection in shotgun proteomics.

Li J et al.

Molecular & Cellular Proteomics : Mcp, 2011

[Correlation of TFRC polymorphism with the susceptibility and clinicopathologic phenotypes of IgA nephropathy].

Feng XZ et al.

Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences, 2008

HFE H63D variant and leukemia susceptibility.

Dorak MT

Leukemia & Lymphoma, 2006

Evidence for an association between compound heterozygosity for germ line mutations in the hemochromatosis (HFE) gene and increased risk of colorectal cancer.

Robinson JP et al.

Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2005

Hemochromatosis gene mutations and distal adenomatous colorectal polyps.

McGlynn KA et al.

Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2005

Preliminary identification of pathogenic variants in an Afro-Colombian Raizal family with risk factors for glaucoma.

Castillo-Plata H et al.

Colombia Medica (cali, Colombia), 0

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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."