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Dataset
Additional file 9: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
Splice-site variants with their corresponding HSF and MaxEnt Scores from Human Splicing Finder 3.0. (XLSX 10 kb)
Publication year:2019
Accessibility:open
Publisher:figshare.ars
License:CC0-1.0,CC-BY-4.0
Format:xlsx
Keywords: familial breast cancer, missing heritability, BRCA1 and BRCA2-negative, whole exome sequencing, candidate breast cancer predisposing genes/variants