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DIS3 is detected as a mutational cancer driver

DIS3 reports

Gene details
DIS3
Gene ID ENSG00000083520
Transcript ID ENST00000377767
Protein ID ENSP00000366997
Cancer types where is driver 1
Cohorts where is driver 1
Mutated samples 10
Mutations 410
Known driver False
Method signals per Cancer Type
Cancer type Methods Samples Samples (%)
ClustL HotMAPS smRegions Clustered Mutations
CBaSE dNdScv Recurrent Mutations
FML Functional Mutations
MutPanning Tri-nucleotide specific bias
combination Combination
In-silico saturation mutagenesis
Alt text
In silico saturation mutagenesis profiles across all tumor types where a specific model is available. Driver mutations (displayed as red dots) are mapped to their positions in the canonical transcript. The dendrogram on the right represents a hierarchical clustering of the profiles based on site-by-site concordance via Matthews Correlation similarity. The track on the top displays the Pfam domains mapping to the canonical transcript. See the FAQs for more details about the in silico saturation mutagenesis computed with boostDM.
Model Mutations Driver mutations Driver mutations (%)
LNM (Lymphoid Neoplasm) 11450 4873 42.56
LYMPH (Lymphoid) 11450 4899 42.79
MBN (Mature B-Cell Neoplasms) 11450 4888 42.69
NHL (Non-Hodgkin Lymphoma) 11450 4894 42.74
PCM (Plasma Cell Myeloma) 11450 4885 42.66
Observed mutations in tumors
The mutations needle plot shows the distribution of the observed mutations along the protein sequence.
Mutation (GRCh38) Protein Position Samples Consequence