Varaico: Literature-Extracted Genetic Variants

Gene:NBN
Variant:p.E23delFs
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NBN

NM_002485.5:p.E23delFs

Associated Papers

Frequency of Founder Mutations in BRCA1 and BRCA2 Genes in Hereditary Breast Cancers in Poland vs. Other Countries.

Kulikowska B et al.

Cancers, 2026

Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan.

Akbar F et al.

Hereditary Cancer in Clinical Practice, 2022

Genetic predisposition to male breast cancer in Poland.

Szwiec M et al.

Bmc Cancer, 2021

Prevalence of pathogenic variants in DNA damage response and repair genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer.

Hartman TR et al.

Scientific Reports, 2020

The spectrum of mutations predisposing to familial breast cancer in Poland.

Cybulski C et al.

International Journal of Cancer, 2019

Landscape of Germline Mutations in DNA Repair Genes for Breast Cancer in Latin America: Opportunities for PARP-Like Inhibitors and Immunotherapy.

Urbina-Jara LK et al.

Genes, 2019

Hereditary breast and ovarian cancer susceptibility genes (review).

Kobayashi H et al.

Oncology Reports, 2013

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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."