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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)
Jaar van publicatie:2019
Toegankelijkheid:open
Uitgever:figshare.ars
Licentie:CC0-1.0,CC-BY-4.0
Formaat:xlsx
Trefwoorden: familial breast cancer, missing heritability, BRCA1 and BRCA2-negative, whole exome sequencing, candidate breast cancer predisposing genes/variants