Varaico: Literature-Extracted Genetic Variants

Gene:SLX4
Variant:p.R237Q
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SLX4

NM_032444.4:p.R237Q

Associated Papers

Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition.

Fiorica PN et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2025

39992227 (PubMed )
Supplement: ccr-24-2785_supplementary_data_1_suppds1.xlsx › Supplemental_Table_3

Alterations in DNA Damage Repair Genes Before and After Neoadjuvant Cisplatin-based Chemotherapy in Muscle-invasive Bladder Cancer.

Lemberger U et al.

European Urology Open Science, 2025

39717660 (PubMed )
Supplement: mmc4.xlsx › Raw_data

Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues.

Sánchez-Guixé M et al.

Cancer Discovery, 2024

38501975 (PubMed )
Supplement: EMS194327-supplement-Table_S1.pdf

Identification of heritable rare variants associated with early-stage lung adenocarcinoma risk.

Fu R et al.

Translational Lung Cancer Research, 2022

35529798 (PubMed )
Supplement: tlcr-11-04-509-supplementary.pdf

A systematic genome-wide mapping of oncogenic mutation selection during CRISPR-Cas9 genome editing.

Sinha S et al.

Nature Communications, 2021

34764240 (PubMed )
Supplement: 41467_2021_26788_MOESM14_ESM.zip › Source_Data › Source_Data_Figure_1-6.xlsx › Figure_6F

Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients.

Del Valle J et al.

Cancers, 2020

32235514 (PubMed )
Supplement: cancers-12-00829-s001.zip › cancers-727310-supplementary › Table_S3.xlsx › Supplementary_Table_3

A novel molecular diagnostics platform for somatic and germline precision oncology.

Cabanillas R et al.

Molecular Genetics & Genomic Medicine, 2017

Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans.

Elmakky A et al.

Current Genomics, 2015

Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families.

Fernández-Rodríguez J et al.

Bmc Cancer, 2012

Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer.

Landwehr R et al.

Breast Cancer Research and Treatment, 2011

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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."