Mutation gene index search

Total number of mutation frequency in cell lines

Cell Line Frequency
BLOOD_Leukemia 107180
BLOOD_Lymphoma 81539
BLOOD_Myeloma 15891
BONE 15945
BREAST 34721
CNS 45242
KIDNEY 15859
LARGE_INTESTINE 180231
LIVER 12280
LUNG_NSCLC_LUAD 59881
LUNG_NSCLC_LUSC 18659
LUNG_SCLC 46363
OESOPHAGUS 22798
OVARY 42656
PANCREAS 18650
SKIN 6668
SOFT_TISSUE 28165
STOMACH 35808
UPPER_AERODIGESTIVE_TRACT 89241
URINARY_TRACT 21346
Total number of mutation frequency in patient samples
Tissue Frequency
ACC (Adrenocortical carcinoma) 5971
BLCA (Bladder Urothelial Carcinoma) 91098
BRCA (Breast invasive carcinoma) 56484
CESC (Cervical squamous cell carcinoma\n and endocervical adenocarcinoma) 75793
CHOL (Cholangiocarcinoma) 2513
COAD (Colon adenocarcinoma) 149446
DLBC (Lymphoid Neoplasm Diffuse \n Large B-cell Lymphoma) 4721
ESCA (Esophageal carcinoma) 25557
GBM (Glioblastoma multiforme) 22125
HNSC (Head and Neck squamous \n cell carcinoma) 62575
KICH (Kidney Chromophobe) 1908
KIRC (Kidney renal clear cell carcinoma) 14021
KIRP (Kidney renal papillary cell carcinoma) 17157
LAML (Acute Myeloid Leukemia) 2060
LGG (Brain Lower Grade Glioma) 23638
LIHC (Liver hepatocellular carcinoma) 39491
LUAD (Lung adenocarcinoma) 107035
LUSC (Lung squamous cell carcinoma) 118771
MESO (Mesothelioma) 2397
OV (Ovarian serous cystadenocarcinoma) 16537
PAAD (Pancreatic adenocarcinoma) 11670
PCPG (Pheochromocytoma and Paraganglioma) 1360
PRAD (Prostate adenocarcinoma) 18830
READ (Rectum adenocarcinoma) 45601
SARC (Sarcoma) 18834
SKCM (Skin Cutaneous Melanoma) 300904
STAD (Stomach adenocarcinoma) 90141
THCA (Thyroid carcinoma) 4035
THYM (Thymoma) 2316
TGCT (Testicular Germ Cell Tumors) 1467
UCEC (Uterine Corpus Endometrial Carcinoma) 689603
UCS (Uterine Carcinosarcoma) 7829
UVM (Uveal Melanoma) 1368
SCLC (Small Cell Lung Cancer) 24785