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PTEN is detected as a mutational cancer driver

PTEN reports

Gene details
PTEN
Gene ID ENSG00000171862
Transcript ID ENST00000371953
Protein ID ENSP00000361021
Cancer types where is driver 38
Cohorts where is driver 78
Mutated samples 1,073
Mutations 1,794
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 (%)
BOWEL (Bowel) 4763 2972 62.40
BRAIN (CNS/Brain) 4763 3031 63.64
BRCA (Invasive Breast Carcinoma) 4763 2509 52.68
BREAST (Breast) 4763 2509 52.68
COADREAD (Colorectal Adenocarcinoma) 4763 2972 62.40
DIFG (Diffuse Glioma) 4763 3005 63.09
BRAIN (Encapsulated Glioma) 4763 3031 63.64
GB (Glioblastoma) 4763 2741 57.55
GBM (Glioblastoma Multiforme) 4763 2505 52.59
KIDNEY (Kidney) 4763 2786 58.49
LUNG (Lung) 4763 2366 49.67
LUSC (Lung Squamous Cell Carcinoma) 4763 2141 44.95
MEL (Melanoma) 4763 2566 53.87
NSCLC (Non-Small Cell Lung Cancer) 4763 2091 43.90
PRAD (Prostate Adenocarcinoma) 4763 2448 51.40
PROSTATE (Prostate) 4763 2451 51.46
RCC (Renal Cell Carcinoma) 4763 2786 58.49
SKIN (Skin) 4763 2537 53.26
UCEC (Endometrial Carcinoma) 4763 2616 54.92
UTERUS (Uterus) 4763 2614 54.88
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