Varaico: Literature-Extracted Genetic Variants

Gene:CTNNB1
Variant:p.G34A
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CTNNB1

NM_001904.4:p.G34A

Associated Papers

Infantile Sinonasal Myxoma Is Clinically and Genetically Distinct From Other Myxomas of the Craniofacial Bones and From Desmoid Fibromatosis.

Odintsov I et al.

The American Journal of Surgical Pathology, 2023

Standing in the canine precision medicine knowledge gap: Improving annotation of canine cancer genomic biomarkers through systematic comparative analysis of human cancer mutations in COSMIC.

Sakthikumar S et al.

Veterinary and Comparative Oncology, 2023

37248814 (PubMed )
Supplement: supplement_1.xlsx › Supp._Table_5

The autism-associated loss of δ-catenin functions disrupts social behavior.

Mendez-Vazquez H et al.

Proceedings of the National Academy of Sciences of the United States of America, 2023

The autism-associated loss of δ-catenin functions disrupts social behaviors.

Mendez-Vazquez H et al.

Biorxiv : the Preprint Server for Biology, 2023

Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis.

Light N et al.

Nature Communications, 2023

36604421 (PubMed )
Supplement: 41467_2022_35727_MOESM5_ESM.xlsx › Sheet1

Targeted Therapy of Papillary Thyroid Cancer: A Comprehensive Genomic Analysis.

Hescheler DA et al.

Frontiers in Endocrinology, 2021

34630336 (PubMed )
Supplement: Table_1.xlsx › Tab2

Analytical Validation of a Hybrid Capture-Based Next-Generation Sequencing Clinical Assay for Genomic Profiling of Cell-Free Circulating Tumor DNA.

Clark TA et al.

The Journal of Molecular Diagnostics : Jmd, 2018

29936259 (PubMed )
Supplement: mmc12.xlsx › Table_S12

Intranodal palisaded myofibroblastoma: another mesenchymal neoplasm with CTNNB1 (β-catenin gene) mutations: clinicopathologic, immunohistochemical, and molecular genetic study of 18 cases.

Laskin WB et al.

The American Journal of Surgical Pathology, 2015

Functional correlates of mutation of the Asp32 and Gly34 residues of beta-catenin.

Provost E et al.

Oncogene, 2005

Genomic and immunohistochemical analysis in human adrenal cortical neoplasia reveal beta-catenin mutations as potential prognostic biomarker.

Kovach AE et al.

Discoveries (craiova, Romania), 0

CTNNB1 somatic mutations drive Wnt pathway activation in a case of incidental intranodal palisaded myofibroblastoma.

Moreno de Juan G et al.

Revista Espanola De Patologia : Publicacion Oficial De La Sociedad Espanola De Anatomia Patologica Y De La Sociedad Espanola De Citologia, 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."