P/LP variants. cDNA and Protein changes are named according to HGVS... | Download Table
Absence of BRCA/FMR1 Correlations in Women with Ovarian Cancers | PLOS ONE
NGS bioinformatics pipeline—worries and wish lists: A look at the preanalytic, analytic, and postanalytic phases - CAP TODAY
Spectrum of the Mutations in <fc>B</fc>ernard–<fc>S</fc>oulier Syndrome
Comprehensive profiling of BRCA1 and BRCA2 variants in breast and ovarian cancer in Chinese patients - Gao - 2020 - Human Mutation - Wiley Online Library
How to read variant information in the rare diseases test reports…
Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients | Oncotarget
Common mutation types of BRCA1 or BRCA2 genes in the BIC database. | Download Scientific Diagram
Genes | Free Full-Text | Differences in Ovarian and Other Cancers Risks by Population and BRCA Mutation Location
Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilate
Functional assays provide a robust tool for the clinical annotation of genetic variants of uncertain significance | npj Genomic Medicine
Reported prevalence of BRCA1 founder mutations in the Polish population. | Download Scientific Diagram
Table 2 from Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea. | Semantic Scholar
BRCA Exchange
Germ line BRCA2 pathogenic mutations in breast and ovarian cancer... | Download Table
Comparative In Vitro and In Silico Analyses of Variants in Splicing Regions of BRCA1 and BRCA2 Genes and Characterization of Novel Pathogenic Mutations | PLOS ONE
My Mutation
Frontiers | Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays
dbBRCA-Asian
![PDF] The Clinical Significance of Unknown Sequence Variants in BRCA Genes | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/bf87f5f3d03688219adbdb700c61ca774b46789f/2-Table1-1.png "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
Reported prevalence of BRCA1 founder mutations in the Polish population. | Download Scientific Diagram
Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project - Genetics in Medicine
Frameshift mutations detected in BRCA genes | Download Table
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?
Frontiers | Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15
The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science
