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Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients | Oncotarget
Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients | Oncotarget

Spectrum of the Mutations in <fc>B</fc>ernard&#x02013;<fc>S</fc>oulier Syndrome
Spectrum of the Mutations in <fc>B</fc>ernard&#x02013;<fc>S</fc>oulier Syndrome

BRCA2 variants identified in the analyzed population by dHPLC/Sanger... | Download Table
BRCA2 variants identified in the analyzed population by dHPLC/Sanger... | Download Table

Table 2 from Suggestion of BRCA1 c.5339T&gt;C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea. | Semantic Scholar
Table 2 from Suggestion of BRCA1 c.5339T&gt;C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea. | Semantic Scholar

Reported prevalence of BRCA1 founder mutations in the Polish population. | Download Scientific Diagram
Reported prevalence of BRCA1 founder mutations in the Polish population. | Download Scientific Diagram

Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife
Figures and data in Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance | eLife

Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?
Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?

Genes | Free Full-Text | BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome
Genes | Free Full-Text | BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome

Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis – topic of research paper in Biological sciences. Download scholarly article PDF
Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis – topic of research paper in Biological sciences. Download scholarly article PDF

My Mutation
My Mutation

Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15
Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15

How to read variant information in the rare diseases test reports…
How to read variant information in the rare diseases test reports…

PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar
PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar

Common mutation types of BRCA1 or BRCA2 genes in the BIC database. | Download Scientific Diagram
Common mutation types of BRCA1 or BRCA2 genes in the BIC database. | Download Scientific Diagram

Cureus | Sociodemographic, Clinical, and Variation Outcomes for Breast Cancer and Breast Cancer-Related Mutations in a Ten-Year Cohort From Neiva, Huila, Colombia | Article
Cureus | Sociodemographic, Clinical, and Variation Outcomes for Breast Cancer and Breast Cancer-Related Mutations in a Ten-Year Cohort From Neiva, Huila, Colombia | Article

dbBRCA-Asian
dbBRCA-Asian

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My Mutation

Frameshift mutations detected in BRCA genes | Download Table
Frameshift mutations detected in BRCA genes | Download Table

The Breast Cancer Information Core: Database design, structure, and scope - Szabo - 2000 - Human Mutation - Wiley Online Library
The Breast Cancer Information Core: Database design, structure, and scope - Szabo - 2000 - Human Mutation - Wiley Online Library

Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays
Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays

Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table
Novel variants of uncertain clinical significance (VUS) in Greek... | Download Table

P/LP variants. cDNA and Protein changes are named according to HGVS... | Download Table
P/LP variants. cDNA and Protein changes are named according to HGVS... | Download Table