Varaico: Literature-Extracted Genetic Variants

Gene:CHEK2
Variant:p.P536P
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CHEK2

NM_007194.4:p.P536P

Associated Papers

Cell-Free DNA Sequencing Reveals Gene Variants in DNA Damage Repair Genes Associated with Prognosis of Prostate Cancer Patients.

Lieb V et al.

Cells, 2022

36429046 (PubMed )
Supplement: cells-11-03618-s001.zip › Suppl._files › Suppl._Table_S2_.xlsx › variant_score

Identification of CHEK2 germline mutations in BRCA1/2 and PALB2 negative breast and ovarian cancer patients.

Aksoy F et al.

Human Heredity, 2022

Cell-Free DNA Variant Sequencing Using Plasma and AR-V7 Testing of Circulating Tumor Cells in Prostate Cancer Patients.

Lieb V et al.

Cells, 2021

34831445 (PubMed )
Supplement: cells-10-03223-s001.zip › Suppl._Table_S1.xlsx › variant_score

A recurrent CHEK2 p.H371Y mutation is associated with breast cancer risk in Chinese women.

Liu Y et al.

Human Mutation, 2011

Evaluation of the contribution of the three breast cancer susceptibility genes CHEK2, STK11, and PALB2 in non-BRCA1/2 French Canadian families with high risk of breast cancer.

Guénard F et al.

Genetic Testing and Molecular Biomarkers, 2010

The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype.

Ruijs MW et al.

Hereditary Cancer in Clinical Practice, 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."