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. 2016 May 14;7(31):50719–50734. doi: 10.18632/oncotarget.9368

Table 2. Overview of SETD2 mutation frequencies in a selection of tumors based on the COSMIC database (Feb 2016)*.

Tissue/tumour subtype Percentage of samples with mutation cases tested
truncating missense
Kidney 4.19 3.10 2197
ccRCC 5.43 4.14 1473
Lung 1.26 1.42 1826
Adenocarcinoma 3.51 3.51 550
Skin 1.08 2.65 1017
Liver 0.74 1.55 1611
Hepatocellular carcinoma 0.78 1.12 893
Soft tissue 0.70 4.67 428
Biliary tract 0.66 0.66 152
Adenocarcinoma 0.67 0.67 150
Endometrium 0.63 3.49 631
Endometrioid carcinoma 0.74 4.08 539
Large intestine 0.59 3.05 1345
Adenocarcinoma 0.62 3.10 1298
Breast 0.58 0.94 1378
Central nervous system 0.47 0.38 2128
Pancreas 0.46 0.33 1521
Ductal carcinoma 0.40 0.57 1240
Stomach 0.34 2.04 587
Urinary tract 0.30 0.90 666
Haematopoietic and lymphoid 0.24 0.87 2519
Acute lymphoblastic B cell leukaemia 1.54 2.32 258
Acute lymphoblastic T cell leukaemia 0.97 0.97 207
Diffuse large B cell lymphoma 0.00 3.20 250
Ovary 0.24 0.59 843
Serous carcinoma 0.31 0.78 641
Bone 0.20 0.60 496
Prostate 0.10 0.88 1019
Adenocarcinoma 0.12 0.48 827
*

Tumor subtypes with a sample size less than 100 cases have been excluded.