Varaico: Literature-Extracted Genetic Variants

Gene:CTNNB1
Variant:p.W383C
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CTNNB1

NM_001904.4:p.W383C

Associated Papers

Integrating evidence from protein domains to identify cancer driver mutations.

Ostroverkhova D et al.

Protein Science : a Publication of the Protein Society, 2026

41556616 (PubMed )
Supplement: PRO-35-e70422-s002.xlsx › Table_S1

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 conformational and mutational landscape of the ubiquitin-like marker for autophagosome formation in cancer.

Fas BA et al.

Autophagy, 2021

33302793 (PubMed )
Supplement: KAUP_A_1847443_SM1965.zip › Supplementary_information › TableS4.xlsx › IID_LIRs_mutations

Genetic alteration of Chinese patients with rectal mucosal melanoma.

Li H et al.

Bmc Cancer, 2021

34044811 (PubMed )
Supplement: 12885_2021_8383_MOESM1_ESM.xlsx › Supplementary_Table_1

Genomic profiling reveals high frequency of DNA repair genetic aberrations in gallbladder cancer.

Abdel-Wahab R et al.

Scientific Reports, 2020

33328484 (PubMed )
Supplement: 41598_2020_77939_MOESM1_ESM.xlsx › Sheet1

Assessment of somatic mutations in urine and plasma of Wilms tumor patients.

Miguez ACK et al.

Cancer Medicine, 2020

Oncogenic Mutations in Armadillo Repeats 5 and 6 of β-Catenin Reduce Binding to APC, Increasing Signaling and Transcription of Target Genes.

Liu P et al.

Gastroenterology, 2020

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour.

Halliday BJ et al.

Plos Genetics, 2018

29912901 (PubMed )
Supplement: pgen.1007399.s002.xlsx › Sheet2

Somatic mutations in CDH1 and CTNNB1 in primary carcinomas at 13 anatomic sites.

Busch EL et al.

Oncotarget, 2017

29156750 (PubMed )
Supplement: oncotarget-08-85680-s002.xlsx › CTNNB1

Canonical WNT signalling determines lineage specificity in Wilms tumour.

Fukuzawa R et al.

Oncogene, 2009

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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."