The mutational landscape of core-binding factor acute myeloid leukemias
Mutational data for 165 CBF-AML cases sequenced either by whole-genome (n = 17) or whole-exome (n = 148) sequencing are displayed. Two fusion subgroups are compared (RUNX1-RUNX1T1 and CBFB-MYH11). Signaling, epigenetic and cohesin genes are separated into functional groups. Cytogenetic abnormalities (Del(9q), -X/-Y, +8, -5/-7, and Complex), patient age group (adult or pediatric), and fusion status are indicated. Visualization representative of Faber, et al. 2016, Figure 1a. Mousing over each instance of a mutation provides further information (sample, mutation type, amino acid change, and gene name). Clicking on each gene symbol opens a ProteinPaint view of mutations found within the gene for this cohort. Numbers in parentheses next to each gene symbol indicate the number of samples altered.