Varaico: Literature-Extracted Genetic Variants

Gene:CHEK2
Variant:p.F169fs
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CHEK2

NM_007194.4:p.F169fs

Associated Papers

Utilization of genetic evaluation in patients with kidney cancer who meet guidelines for genetic referral.

Makarova E et al.

Urologic Oncology, 2025

Germline CHEK2 mutations in patients with myeloid neoplasms.

Freiman L et al.

Leukemia, 2024

Immunohistochemical findings and clinicopathological features of breast cancers with pathogenic germline mutations in Non-BRCA genes.

Singh K et al.

Human Pathology, 2024

Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer.

Turchiano A et al.

Genes, 2023

Identification of hereditary breast and ovarian cancer germline variants in Granada (Spain): NGS perspective.

Molina-Zayas M et al.

Molecular Genetics and Genomics : Mgg, 2022

Functional Analysis Identifies Damaging CHEK2 Missense Variants Associated with Increased Cancer Risk.

Boonen RACM et al.

Cancer Research, 2022

Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.

LaDuca H et al.

Plos One, 2017

28152038 (PubMed )
Supplement: pone.0170843.s003.xlsx › S3_Table
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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."