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PAX5 is detected as a mutational cancer driver

PAX5 reports

Gene details
PAX5
Gene ID ENSG00000196092
Transcript ID ENST00000358127
Protein ID ENSP00000350844
Cancer types where is driver 2
Cohorts where is driver 2
Mutated samples 6
Mutations 280
Known driver True
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) 4796 2968 61.88
LYMPH (Lymphoid) 4796 3086 64.35
NHL (Non-Hodgkin Lymphoma) 4796 3088 64.39
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