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TP53 is detected as a mutational cancer driver

TP53 reports

Gene details
TP53
Gene ID ENSG00000141510
Transcript ID ENST00000269305
Protein ID ENSP00000269305
Cancer types where is driver 74
Cohorts where is driver 212
Mutated samples 9,192
Mutations 11,353
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 (%)
SKIN (Basal Cell Carcinoma) 4823 1332 27.62
BILIARY_TRACT (Biliary Tract) 4823 1084 22.48
MBN (Burkitt Lymphoma) 4823 923 19.14
BLADDER (Bladder/Urinary Tract) 4823 1115 23.12
BLCA (Bladder Urothelial Carcinoma) 4823 981 20.34
BONE (Bone) 4823 1139 23.62
BOWEL (Bowel) 4823 933 19.34
BRAIN (CNS/Brain) 4823 915 18.97
BRCA (Invasive Breast Carcinoma) 4823 755 15.65
BREAST (Breast) 4823 755 15.65
CHOL (Cholangiocarcinoma) 4823 1094 22.68
RCC (Chromophobe Renal Cell Carcinoma) 4823 1364 28.28
MBN (Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma) 4823 917 19.01
COAD (Colon Adenocarcinoma) 4823 819 16.98
COADREAD (Colorectal Adenocarcinoma) 4823 901 18.68
CSCC (Cutaneous Squamous Cell Carcinoma) 4823 1352 28.03
DIFG (Diffuse Glioma) 4823 948 19.66
DLBCLNOS (Diffuse Large B-Cell Lymphoma, NOS) 4823 1052 21.81
EGC (Esophagogastric Adenocarcinoma) 4823 854 17.71
ENCG (Encapsulated Glioma) 4823 776 16.09
ESCA (Esophageal Adenocarcinoma) 4823 701 14.53
ESCC (Esophageal Squamous Cell Carcinoma) 4823 617 12.79
GB (Glioblastoma) 4823 938 19.45
GBM (Glioblastoma Multiforme) 4823 949 19.68
HCC (Hepatocellular Carcinoma) 4823 1108 22.97
HEAD_NECK (Head and Neck) 4823 911 18.89
HGGNOS (High-Grade Glioma, NOS) 4823 747 15.49
HNSC (Head and Neck Squamous Cell Carcinoma) 4823 789 16.36
IPN (Intraductal Papillary Neoplasm of the Bile Duct) 4823 1094 22.68
KIDNEY (Kidney) 4823 1466 30.40
LGGNOS (Low-Grade Glioma, NOS) 4823 604 12.52
LIVER (Liver) 4823 1104 22.89
LMS (Leiomyosarcoma) 4823 1193 24.74
LNET (Lung Neuroendocrine Tumor) 4823 910 18.87
LNM (Lymphoid Neoplasm) 4823 913 18.93
LUAD (Lung Adenocarcinoma) 4823 907 18.81
LUNG (Lung) 4823 961 19.93
LUSC (Lung Squamous Cell Carcinoma) 4823 810 16.79
LYMPH (Lymphoid) 4823 917 19.01
MBN (Mature B-Cell Neoplasms) 4823 941 19.51
BRAIN (Miscellaneous Brain Tumor) 4823 835 17.31
MEL (Melanoma) 4823 1212 25.13
RCC (Renal Non-Clear Cell Carcinoma) 4823 1364 28.28
NHL (Non-Hodgkin Lymphoma) 4823 925 19.18
NPC (Nasopharyngeal Carcinoma) 4823 901 18.68
NSCLC (Non-Small Cell Lung Cancer) 4823 926 19.20
OS (Osteosarcoma) 4823 1196 24.80
OVARY (Ovary/Fallopian Tube) 4823 777 16.11
OVT (Ovarian Epithelial Tumor) 4823 781 16.19
PAAD (Pancreatic Adenocarcinoma) 4823 929 19.26
PANCREAS (Pancreas) 4823 892 18.49
ENCG (Pilocytic Astrocytoma) 4823 655 13.58
PCM (Plasma Cell Myeloma) 4823 1117 23.16
PRAD (Prostate Adenocarcinoma) 4823 676 14.02
PROSTATE (Prostate) 4823 827 17.15
RCC (Renal Cell Carcinoma) 4823 1364 28.28
READ (Rectal Adenocarcinoma) 4823 1238 25.67
SCLC (Small Cell Lung Cancer) 4823 927 19.22
MEL (Cutaneous Melanoma) 4823 1212 25.13
SKIN (Skin) 4823 1332 27.62
SOFT_TISSUE (Soft Tissue) 4823 1140 23.64
STAD (Stomach Adenocarcinoma) 4823 854 17.71
STOMACH (Esophagus/Stomach) 4823 878 18.20
UCEC (Endometrial Carcinoma) 4823 796 16.50
UCS (Uterine Carcinosarcoma/Uterine Malignant Mixed Mullerian Tumor) 4823 837 17.35
UTERUS (Uterus) 4823 796 16.50
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