Varaico: Literature-Extracted Genetic Variants

Gene:U2AF1
Variant:p.I24T
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U2AF1

NM_006758.3:p.I24T

Associated Papers

U2AF1 mutations rescue deleterious exon skipping induced by KRAS mutations.

Walter DM et al.

Biorxiv : the Preprint Server for Biology, 2025

The effect of U2AF1 mutation on erythroid differentiation and sensitivity to demethylation drug treatment.

Liu Y et al.

Medical Oncology (northwood, London, England), 2025

Reannotation of cancer mutations based on expressed RNA transcripts reveals functional non-coding mutations in melanoma.

Pepe D et al.

American Journal of Human Genetics, 2025

40359938 (PubMed )
Supplement: mmc6.xlsx › Sheet_1

TP53 missense mutation reveals gain-of-function properties in small-sized KRAS transformed pancreatic ductal adenocarcinoma.

Zhou Y et al.

Journal of Translational Medicine, 2023

38037073 (PubMed )
Supplement: 12967_2023_4742_MOESM1_ESM.xlsx › Sheet1

The Biological and Clinical Consequences of RNA Splicing Factor U2AF1 Mutation in Myeloid Malignancies.

Zhao Y et al.

Cancers, 2022

The genetic landscape of pancreatic head ductal adenocarcinoma in China and prognosis stratification.

Yang Y et al.

Bmc Cancer, 2022

35180847 (PubMed )
Supplement: 12885_2022_9279_MOESM3_ESM.xlsx › sheet1

Clinical and molecular characteristics of Chinese non-small cell lung cancer patients with ERBB2 transmembrane domain mutations.

Fan Y et al.

Molecular Oncology, 2020

32478891 (PubMed )
Supplement: MOL2-14-1731-s002.xlsx › Sheet1

Rare and private spliceosomal gene mutations drive partial, complete, and dual phenocopies of hotspot alterations.

Pangallo J et al.

Blood, 2020

A novel 3' splice site recognition by the two zinc fingers in the U2AF small subunit.

Yoshida H et al.

Genes & Development, 2015

26215567 (PubMed )
Supplement: supp_gad.267104.115_SuppMaterial.pdf
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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."