Varaico: Literature-Extracted Genetic Variants

Gene:BRCA2
Variant:p.S1093delFs
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BRCA2

NM_000059.4:p.S1093delFs

Associated Papers

Three cases of colon cancer in four generations of the Saudi family, caused by endogamous germline mutations.

Alshaya DS et al.

Cellular and Molecular Biology (noisy-le-grand, France), 2023

Increased prevalence of the founder BRCA1 c.5309G>T and recurrent BRCA2 c.1310_1313delAAGA mutations in breast cancer families from Northerstern region of Morocco: evidence of geographical specificity and high relevance for genetic counseling.

Melki R et al.

Bmc Cancer, 2023

Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients.

Jouhadi H et al.

Bmc Research Notes, 2016

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients.

El Khachibi M et al.

Bmc Cancer, 2015

BRCA1 and BRCA2 germline mutation spectrum in hereditary breast/ovarian cancer families from Maghrebian countries.

Cherbal F et al.

Breast Disease, 2012

Contribution of BRCA2 germline mutations to hereditary breast/ovarian cancer in Germany.

Hamann U et al.

Journal of Medical Genetics, 2002

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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."