Varaico: Literature-Extracted Genetic Variants

Gene:H3-3A
Variant:p.G35W
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H3-3A

NM_002107.7:p.G35W

Associated Papers

β-Human Chorionic Gonadotropin-Secreting Giant Cell Tumor of Bone in the Mandible: Case Report and Comprehensive Literature Review.

Flores-Hidalgo A et al.

Head and Neck Pathology, 2026

H3-3A gene mutation analysis in giant cell tumor of bone and its histologic mimics: A single institutional study from India.

Uppin SG et al.

Annals of Diagnostic Pathology, 2026

Comparative Analysis of a Dual DNA-RNA Panel and a DNA-Only Panel for Sarcoma: Real-World Data From a Nationwide Genomic Database.

Nakata E et al.

Cancer Science, 2026

41128349 (PubMed )
Supplement: CAS-117-156-s003.xlsx › Sheet1

Nucleotide Substitution Biases in Related Cancer Driver Genes.

Khadre A et al.

International Journal of Molecular Sciences, 2025

Genomic profiling in hepatocellular carcinoma: a real-world retrospective analysis.

Salani F et al.

Esmo Open, 2025

41167083 (PubMed )
Supplement: mmc4.xlsx › Table_S10B

Conventional (bone-type) giant cell tumor of the larynx: the first case with proven H3-3A: c.103G >T (p.Gly35Trp) mutation.

Laco J et al.

Virchows Archiv : an International Journal of Pathology, 2025

Establishment and characterization of two novel patient-derived cell lines from giant cell tumor of bone: NCC-GCTB11-C1 and NCC-GCTB12-C1.

Adachi Y et al.

Human Cell, 2025

Genetics of urinary bladder paragangliomas: a multi-center study of a Chinese cohort.

Jiang J et al.

Journal of Endocrinological Investigation, 2025

Insights into the genetic landscape of pheochromocytomas and paragangliomas in a Brazilian cohort.

Fagundes GFC et al.

European Journal of Endocrinology, 2025

A Rare Pediatric Giant Cell Tumor of the Clivus Bone, H3.3 p.Gly35Trp-mutated: Case Report and Mini-review of the Literature.

Gaggero G et al.

Turkish Archives of Pediatrics, 2025

Genomic Insights Into High-Grade Infarct-Associated Bone Sarcomas.

Tvrdik T et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc, 2024

GLI1 confers resistance to PARP inhibitors by activating the DNA damage repair pathway.

Ikeuchi H et al.

Oncogene, 2024

39095584 (PubMed )
Supplement: 41388_2024_3105_MOESM2_ESM.xlsx › Supplementary_Table_S6

H3.3-G34W in giant cell tumor of bone functionally aligns with the exon choice repressor hnRNPA1L2.

Lee E et al.

Cancer Gene Therapy, 2024

Osteosarcomas With Few Chromosomal Alterations or Adult Onset Are Genetically Heterogeneous.

Difilippo V et al.

Laboratory Investigation; a Journal of Technical Methods and Pathology, 2024

Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment.

Zethoven M et al.

Nature Communications, 2022

36271074 (PubMed )
Supplement: 41467_2022_34011_MOESM4_ESM.xlsx › Supplementary_Data_1

Clinicopathologic and molecular features of denosumab-treated giant cell tumour of bone (GCTB): Analysis of 21 cases.

Yang L et al.

Annals of Diagnostic Pathology, 2022

Diagnostic Utility of Genetic and Immunohistochemical H3-3A Mutation Analysis in Giant Cell Tumour of Bone.

Wągrodzki M et al.

International Journal of Molecular Sciences, 2022

A Comprehensive Understanding of the Genomic Bone Tumor Landscape: A Multicenter Prospective Study.

Xie X et al.

Frontiers in Oncology, 2022

Mutational Profile and Potential Molecular Therapeutic Targets of Pheochromocytoma.

Ma X et al.

Frontiers in Endocrinology, 2022

A common classification framework for histone sequence alterations in tumours: an expert consensus proposal.

Leske H et al.

The Journal of Pathology, 2021

Electronic DNA Analysis of CSF Cell-free Tumor DNA to Quantify Multi-gene Molecular Response in Pediatric High-grade Glioma.

Bruzek AK et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2020

Globally altered epigenetic landscape and delayed osteogenic differentiation in H3.3-G34W-mutant giant cell tumor of bone.

Lutsik P et al.

Nature Communications, 2020

Absence of H3F3A mutation in a subset of malignant giant cell tumor of bone.

Yoshida KI et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc, 2019

[H3F3A mutated multicentric giant cell tumor of bone : A very rare primary bone disease].

Giesche JP et al.

Der Pathologe, 2018

The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location.

Scotto di Carlo F et al.

Bmc Cancer, 2018

Detection of H3F3A p.G35W and p.G35R in giant cell tumor of bone by Allele Specific Locked Nucleic Acid quantitative PCR (ASLNAqPCR).

Gamberi G et al.

Pathology, Research and Practice, 2018

Update of Pheochromocytoma Syndromes: Genetics, Biochemical Evaluation, and Imaging.

Alrezk R et al.

Frontiers in Endocrinology, 2018

Highly recurrent H3F3A mutations with additional epigenetic regulator alterations in giant cell tumor of bone.

Ogura K et al.

Genes, Chromosomes & Cancer, 2017

Histone 3.3 mutations in giant cell tumor and giant cell-rich sarcomas of bone.

Righi A et al.

Human Pathology, 2017

H3F3 mutation status of giant cell tumors of the bone, chondroblastomas and their mimics: a combined high resolution melting and pyrosequencing approach.

Kervarrec T et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc, 2017

Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas.

Toledo RA et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2016

Denosumab treated giant cell tumour of bone: a morphological, immunohistochemical and molecular analysis of a series.

Girolami I et al.

Journal of Clinical Pathology, 2016

Bilateral Lung Metastases From a Phalangeal Giant Cell Tumor of Bone.

Orr A et al.

Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society, 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."