ENSG00000134982 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000134982 -0.4 5.55e-11 BRCA
ENSG00000134982 -0.8 1.89e-25 LUSC
ENSG00000134982 -0.6 5.29e-16 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000134982 GI tumors 10096563
ENSG00000134982 tumor 10347231
ENSG00000134982 tumour 10559900
ENSG00000134982 tumor 10681393
ENSG00000134982 cancer 10692769
ENSG00000134982 colon cancer 10982392
ENSG00000134982 colon cancer 11166179
ENSG00000134982 colorectal cancer 11211307
ENSG00000134982 colon cancer 11398198
ENSG00000134982 tumours 11514192
ENSG00000134982 cancer 11564862
ENSG00000134982 tumor 12955080
ENSG00000134982 tumour 14596806
ENSG00000134982 tumor 14600025
ENSG00000134982 colon cancer 14728717
ENSG00000134982 Tumor 15958564
ENSG00000134982 colon cancer 16042576
ENSG00000134982 cancer 18160396
ENSG00000134982 tumor 18182737
ENSG00000134982 colorectal tumors 18952824
ENSG00000134982 tumor 21457491
ENSG00000134982 Wilms' tumor 22199344
ENSG00000134982 cancer 23170979
ENSG00000134982 tumor 24928580
ENSG00000134982 cancer 25601154
ENSG00000134982 tumour 25788329
ENSG00000134982 colon tumor 27485505
ENSG00000134982 tumour 28134256
ENSG00000134982 colorectal cancer 28271271
ENSG00000134982 colorectal cancer 29158781
ENSG00000134982 colorectal tumors 8033082
ENSG00000134982 tumour 9348288
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000134982 colorectal adenocarcinoma frameshift_variant 49.18% (2322/4721) 57 entries
ENSG00000134982 colon adenocarcinoma sequence_alteration 47.74% (1182/2476) 19 entries
ENSG00000134982 colorectal neoplasm frameshift_variant 20.93% (104/497) 2 entries
ENSG00000134982 colorectal adenoma missense_variant 49.96% (710/1421) 3 entries
ENSG00000134982 colorectal adenocarcinoma conservative_inframe_deletion 49.18% (2322/4721) 1 entry
ENSG00000134982 rectal adenocarcinoma missense_variant 60.51% (613/1013) 11 entries
ENSG00000134982 Gastric Adenoma stop_gained 33.33% (77/231) 6 entries
ENSG00000134982 Rectal Villous Adenoma missense_variant 83.33% (10/12) 2 entries
ENSG00000134982 colon adenoma frameshift_variant 61.54% (64/104) 7 entries
ENSG00000134982 Ampulla of Vater Carcinoma missense_variant 24.87% (49/197) 1 entry
ENSG00000134982 colorectal adenoma stop_gained 49.96% (710/1421) 16 entries
ENSG00000134982 Rectal Tubulovillous Adenoma frameshift_variant 86.67% (13/15) 2 entries
ENSG00000134982 colorectal adenocarcinoma missense_variant 49.18% (2322/4721) 39 entries
ENSG00000134982 rectum adenoma frameshift_variant 68.42% (13/19) 2 entries
ENSG00000134982 colon adenocarcinoma missense_variant 47.74% (1182/2476) 22 entries
ENSG00000134982 colon adenoma sequence_alteration 61.54% (64/104) 2 entries
ENSG00000134982 colorectal adenoma frameshift_variant 49.96% (710/1421) 14 entries
ENSG00000134982 Rectal Tubular Adenoma stop_gained 62.96% (17/27) 1 entry
ENSG00000134982 rectum adenoma stop_gained 68.42% (13/19) 3 entries
ENSG00000134982 colorectal tubulovillous adenoma frameshift_variant 62.5% (35/56) 4 entries
ENSG00000134982 Rectal Villous Adenoma stop_gained 83.33% (10/12) 3 entries
ENSG00000134982 colonic neoplasm stop_gained 70.0% (14/20) 1 entry
ENSG00000134982 Ampulla of Vater Carcinoma stop_gained 24.87% (49/197) 1 entry
ENSG00000134982 Gastric Adenoma frameshift_variant 33.33% (77/231) 9 entries
ENSG00000134982 rectal adenocarcinoma frameshift_variant 60.51% (613/1013) 24 entries
ENSG00000134982 cecum adenocarcinoma missense_variant 55.73% (219/393) 9 entries
ENSG00000134982 rectal adenocarcinoma stop_gained 60.51% (613/1013) 30 entries
ENSG00000134982 cecum adenocarcinoma frameshift_variant 55.73% (219/393) 16 entries
ENSG00000134982 rectal adenocarcinoma sequence_alteration 60.51% (613/1013) 8 entries
ENSG00000134982 colon adenocarcinoma frameshift_variant 47.74% (1182/2476) 43 entries
ENSG00000134982 colorectal adenoma sequence_alteration 49.96% (710/1421) 7 entries
ENSG00000134982 cecum adenocarcinoma stop_gained 55.73% (219/393) 14 entries
ENSG00000134982 Rectal Villous Adenoma frameshift_variant 83.33% (10/12) 3 entries
ENSG00000134982 Gastric Adenoma sequence_alteration 33.33% (77/231) 2 entries
ENSG00000134982 colorectal adenocarcinoma sequence_alteration 49.18% (2322/4721) 27 entries
ENSG00000134982 cecum adenocarcinoma sequence_alteration 55.73% (219/393) 2 entries
ENSG00000134982 Rectal Tubular Adenoma frameshift_variant 62.96% (17/27) 4 entries
ENSG00000134982 colonic neoplasm frameshift_variant 70.0% (14/20) 2 entries
ENSG00000134982 Rectal Tubulovillous Adenoma stop_gained 86.67% (13/15) 1 entry
ENSG00000134982 colorectal adenoma conservative_inframe_deletion 49.96% (710/1421) 2 entries
ENSG00000134982 Gastric Adenoma missense_variant 33.33% (77/231) 2 entries
ENSG00000134982 colorectal tubulovillous adenoma sequence_alteration 62.5% (35/56) 2 entries
ENSG00000134982 colorectal tubulovillous adenoma stop_gained 62.5% (35/56) 3 entries
ENSG00000134982 Ampulla of Vater Carcinoma frameshift_variant 24.87% (49/197) 1 entry
ENSG00000134982 colorectal adenocarcinoma stop_gained 49.18% (2322/4721) 61 entries
ENSG00000134982 colon adenocarcinoma stop_gained 47.74% (1182/2476) 52 entries
ENSG00000134982 colon adenoma stop_gained 61.54% (64/104) 8 entries
ENSG00000134982 colorectal neoplasm stop_gained 20.93% (104/497) 3 entries
ENSG00000134982 Prostate Small Cell Carcinoma frameshift_variant 15.79% (3/19) 1 entry
ENSG00000134982 Gallbladder Adenocarcinoma missense_variant 3.017% (7/232) 2 entries
ENSG00000134982 esophageal squamous cell carcinoma stop_gained 2.583% (24/929) 2 entries
ENSG00000134982 clear cell renal carcinoma sequence_alteration 0.9793% (17/1736) 1 entry
ENSG00000134982 bladder carcinoma frameshift_variant 4.545% (28/616) 1 entry
ENSG00000134982 lung adenocarcinoma stop_gained 3.746% (121/3230) 5 entries
ENSG00000134982 acute lymphoblastic leukemia missense_variant 0.8264% (3/363) 2 entries
ENSG00000134982 squamous cell lung carcinoma missense_variant 2.317% (25/1079) 5 entries
ENSG00000134982 Rectal Tubulovillous Adenoma sequence_alteration 86.67% (13/15) 1 entry
ENSG00000134982 colonic neoplasm sequence_alteration 70.0% (14/20) 1 entry
ENSG00000134982 Endometrial Endometrioid Adenocarcinoma missense_variant 5.997% (46/767) 3 entries
ENSG00000134982 hepatocellular carcinoma stop_gained 2.661% (29/1090) 3 entries
ENSG00000134982 ovarian serous adenocarcinoma missense_variant 1.396% (13/931) 2 entries
ENSG00000134982 polycythemia vera missense_variant 2.609% (3/115) 2 entries
ENSG00000134982 clear cell renal carcinoma missense_variant 0.9793% (17/1736) 6 entries
ENSG00000134982 Signet Ring Cell Gastric Adenocarcinoma frameshift_variant 7.895% (3/38) 2 entries
ENSG00000134982 colon carcinoma frameshift_variant 25.0% (2/8) 1 entry
ENSG00000134982 Ovarian Endometrioid Adenocarcinoma frameshift_variant 9.589% (7/73) 2 entries
ENSG00000134982 Breast Carcinoma by Gene Expression Profile missense_variant 4.386% (5/114) 4 entries
ENSG00000134982 prostate carcinoma stop_gained 3.901% (22/564) 3 entries
ENSG00000134982 gastric adenocarcinoma frameshift_variant 4.46% (97/2175) 9 entries
ENSG00000134982 bladder transitional cell carcinoma stop_gained 4.733% (31/655) 2 entries
ENSG00000134982 prostate carcinoma missense_variant 3.901% (22/564) 3 entries
ENSG00000134982 prostate carcinoma frameshift_variant 3.901% (22/564) 2 entries
ENSG00000134982 Pancreatic Acinar Cell Carcinoma missense_variant 7.609% (7/92) 2 entries
ENSG00000134982 sebaceous adenocarcinoma missense_variant 37.5% (3/8) 1 entry
ENSG00000134982 central nervous system primitive neuroectodermal neoplasm missense_variant 0.9831% (7/712) 2 entries
ENSG00000134982 Colon Juvenile Polyp missense_variant 25.0% (3/12) 1 entry
ENSG00000134982 diffuse gastric adenocarcinoma stop_gained 16.04% (30/187) 3 entries
ENSG00000134982 nasopharyngeal squamous cell carcinoma stop_gained 2.597% (8/308) 1 entry
ENSG00000134982 Pleural Epithelioid Mesothelioma frameshift_variant 1.442% (3/208) 1 entry
ENSG00000134982 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma stop_gained 2.765% (12/434) 2 entries
ENSG00000134982 angiosarcoma missense_variant 6.383% (3/47) 1 entry
ENSG00000134982 adrenal cortex carcinoma stop_gained 1.691% (7/414) 3 entries
ENSG00000134982 undifferentiated pleomorphic sarcoma missense_variant 4.167% (3/72) 1 entry
ENSG00000134982 chromophobe renal cell carcinoma missense_variant 1.235% (2/162) 2 entries
ENSG00000134982 prostate adenocarcinoma missense_variant 5.326% (120/2253) 4 entries
ENSG00000134982 Hepatoblastoma missense_variant 23.08% (9/39) 1 entry
ENSG00000134982 female breast carcinoma missense_variant 1.518% (9/593) 5 entries
ENSG00000134982 anaplastic astrocytoma missense_variant 2.516% (4/159) 1 entry
ENSG00000134982 follicular thyroid carcinoma missense_variant 3.704% (4/108) 2 entries
ENSG00000134982 Ovarian Endometrioid Adenocarcinoma missense_variant 9.589% (7/73) 2 entries
ENSG00000134982 Endometrial Endometrioid Adenocarcinoma frameshift_variant 5.997% (46/767) 3 entries
ENSG00000134982 breast adenosis stop_gained 16.67% (2/12) 1 entry
ENSG00000134982 lung adenocarcinoma frameshift_variant 3.746% (121/3230) 6 entries
ENSG00000134982 small cell lung carcinoma stop_gained 3.025% (17/562) 1 entry
ENSG00000134982 bile duct adenocarcinoma missense_variant 2.494% (20/802) 3 entries
ENSG00000134982 hepatocellular carcinoma missense_variant 2.661% (29/1090) 4 entries
ENSG00000134982 breast ductal adenocarcinoma stop_gained 3.889% (73/1877) 3 entries
ENSG00000134982 Rectal Traditional Serrated Adenoma frameshift_variant 17.24% (5/29) 1 entry
ENSG00000134982 bladder carcinoma missense_variant 4.545% (28/616) 1 entry
ENSG00000134982 small intestinal adenocarcinoma stop_gained 19.0% (19/100) 5 entries
ENSG00000134982 nasal cavity and paranasal sinus carcinoma missense_variant 10.91% (6/55) 2 entries
ENSG00000134982 Appendix Neuroendocrine Tumor G1 missense_variant 2.128% (2/94) 1 entry
ENSG00000134982 lung adenocarcinoma missense_variant 3.746% (121/3230) 14 entries
ENSG00000134982 esophageal adenocarcinoma frameshift_variant 5.928% (38/641) 3 entries
ENSG00000134982 melanoma stop_gained 3.077% (28/910) 4 entries
ENSG00000134982 rectum adenoma sequence_alteration 68.42% (13/19) 1 entry
ENSG00000134982 papillary thyroid carcinoma frameshift_variant 3.698% (24/649) 7 entries
ENSG00000134982 oral squamous cell carcinoma missense_variant 2.477% (8/323) 4 entries
ENSG00000134982 T-cell acute lymphoblastic leukemia missense_variant 2.658% (16/602) 2 entries
ENSG00000134982 Appendix Adenocarcinoma stop_gained 1.431% (8/559) 2 entries
ENSG00000134982 skin melanoma missense_variant 6.061% (76/1254) 10 entries
ENSG00000134982 anaplastic oligodendroglioma missense_variant 4.082% (4/98) 2 entries
ENSG00000134982 Bladder Adenocarcinoma stop_gained 13.64% (3/22) 2 entries
ENSG00000134982 brain glioblastoma frameshift_variant 1.845% (28/1518) 2 entries
ENSG00000134982 Endometrial Endometrioid Adenocarcinoma stop_gained 5.997% (46/767) 2 entries
ENSG00000134982 Duodenal Adenocarcinoma stop_gained 18.29% (15/82) 2 entries
ENSG00000134982 esophageal carcinoma frameshift_variant 1.363% (14/1027) 1 entry
ENSG00000134982 endometrial carcinoma stop_gained 5.0% (4/80) 3 entries
ENSG00000134982 squamous cell lung carcinoma sequence_alteration 2.317% (25/1079) 1 entry
ENSG00000134982 Dysplasia in Ulcerative Colitis missense_variant 37.5% (3/8) 1 entry
ENSG00000134982 mucosal melanoma missense_variant 4.286% (3/70) 1 entry
ENSG00000134982 pancreatic neuroendocrine tumor missense_variant 3.689% (9/244) 3 entries
ENSG00000134982 nasopharyngeal squamous cell carcinoma sequence_alteration 2.597% (8/308) 1 entry
ENSG00000134982 cervical squamous cell carcinoma missense_variant 2.286% (8/350) 1 entry
ENSG00000134982 breast ductal adenocarcinoma missense_variant 3.889% (73/1877) 3 entries
ENSG00000134982 small intestinal adenocarcinoma frameshift_variant 19.0% (19/100) 5 entries
ENSG00000134982 head and neck squamous cell carcinoma missense_variant 0.6378% (5/784) 2 entries
ENSG00000134982 colorectal neoplasm amino_acid_insertion 20.93% (104/497) 1 entry
ENSG00000134982 acute myeloid leukemia missense_variant 0.5274% (5/948) 1 entry
ENSG00000134982 HER2 Positive Breast Carcinoma missense_variant 6.699% (14/209) 3 entries
ENSG00000134982 lung adenocarcinoma sequence_alteration 3.746% (121/3230) 4 entries
ENSG00000134982 gastric intestinal type adenocarcinoma missense_variant 7.117% (20/281) 4 entries
ENSG00000134982 papillary thyroid carcinoma missense_variant 3.698% (24/649) 2 entries
ENSG00000134982 Pleural Mesothelioma missense_variant 1.351% (2/148) 2 entries
ENSG00000134982 ulcerative colitis missense_variant 3.448% (2/58) 1 entry
ENSG00000134982 Gallbladder Adenocarcinoma stop_gained 3.017% (7/232) 2 entries
ENSG00000134982 ameloblastoma missense_variant 12.0% (3/25) 1 entry
ENSG00000134982 adrenal cortex carcinoma frameshift_variant 1.691% (7/414) 2 entries
ENSG00000134982 prostate adenocarcinoma stop_gained 5.326% (120/2253) 4 entries
ENSG00000134982 adrenal cortex carcinoma missense_variant 1.691% (7/414) 2 entries
ENSG00000134982 ovarian teratoma missense_variant 6.897% (4/58) 1 entry
ENSG00000134982 urothelial carcinoma missense_variant 3.488% (3/86) 1 entry
ENSG00000134982 skin carcinoma missense_variant 7.692% (8/104) 1 entry
ENSG00000134982 rectal neoplasm stop_gained 80.0% (4/5) 1 entry
ENSG00000134982 basal cell carcinoma missense_variant 9.639% (8/83) 2 entries
ENSG00000134982 skin melanoma frameshift_variant 6.061% (76/1254) 2 entries
ENSG00000134982 metaplastic breast carcinoma stop_gained 4.795% (7/146) 2 entries
ENSG00000134982 female breast carcinoma sequence_alteration 1.518% (9/593) 1 entry
ENSG00000134982 papillary renal cell carcinoma missense_variant 0.7732% (3/388) 1 entry
ENSG00000134982 squamous cell lung carcinoma stop_gained 2.317% (25/1079) 2 entries
ENSG00000134982 hepatocellular carcinoma sequence_alteration 2.661% (29/1090) 1 entry
ENSG00000134982 non-small cell lung carcinoma frameshift_variant 1.312% (10/762) 1 entry
ENSG00000134982 prostate adenocarcinoma sequence_alteration 5.326% (120/2253) 1 entry
ENSG00000134982 colon adenoma missense_variant 61.54% (64/104) 1 entry
ENSG00000134982 pancreatic ductal adenocarcinoma missense_variant 3.12% (64/2051) 6 entries
ENSG00000134982 non-small cell lung carcinoma missense_variant 1.312% (10/762) 5 entries
ENSG00000134982 gastric adenocarcinoma stop_gained 4.46% (97/2175) 9 entries
ENSG00000134982 metaplastic breast carcinoma missense_variant 4.795% (7/146) 1 entry
ENSG00000134982 cervical carcinoma missense_variant 12.5% (3/24) 2 entries
ENSG00000134982 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma missense_variant 2.765% (12/434) 5 entries
ENSG00000134982 brain glioblastoma missense_variant 1.845% (28/1518) 6 entries
ENSG00000134982 Duodenal Adenocarcinoma frameshift_variant 18.29% (15/82) 2 entries
ENSG00000134982 melanoma missense_variant 3.077% (28/910) 6 entries
ENSG00000134982 skin melanoma stop_gained 6.061% (76/1254) 2 entries
ENSG00000134982 gastric adenocarcinoma missense_variant 4.46% (97/2175) 6 entries
ENSG00000134982 small intestinal adenocarcinoma missense_variant 19.0% (19/100) 2 entries
ENSG00000134982 papillary thyroid carcinoma stop_gained 3.698% (24/649) 2 entries
ENSG00000134982 adenosquamous lung carcinoma missense_variant 6.897% (2/29) 2 entries
ENSG00000134982 urothelial carcinoma stop_gained 3.488% (3/86) 1 entry
ENSG00000134982 breast carcinoma missense_variant 1.258% (25/1988) 5 entries
ENSG00000134982 bile duct adenocarcinoma stop_gained 2.494% (20/802) 3 entries
ENSG00000134982 pancreatic ductal adenocarcinoma sequence_alteration 3.12% (64/2051) 1 entry
ENSG00000134982 melanoma frameshift_variant 3.077% (28/910) 1 entry
ENSG00000134982 Pancreatic Acinar Cell Carcinoma frameshift_variant 7.609% (7/92) 2 entries
ENSG00000134982 small cell lung carcinoma missense_variant 3.025% (17/562) 4 entries
ENSG00000134982 breast carcinoma frameshift_variant 1.258% (25/1988) 1 entry
ENSG00000134982 breast carcinoma stop_gained 1.258% (25/1988) 1 entry
ENSG00000134982 Merkel cell skin cancer missense_variant 3.509% (6/171) 2 entries
ENSG00000134982 gastric intestinal type adenocarcinoma stop_gained 7.117% (20/281) 3 entries
ENSG00000134982 diffuse gastric adenocarcinoma missense_variant 16.04% (30/187) 2 entries
ENSG00000134982 colorectal tubulovillous adenoma missense_variant 62.5% (35/56) 1 entry
ENSG00000134982 breast ductal adenocarcinoma sequence_alteration 3.889% (73/1877) 1 entry
ENSG00000134982 nasopharyngeal squamous cell carcinoma missense_variant 2.597% (8/308) 2 entries
ENSG00000134982 pancreatic ductal adenocarcinoma stop_gained 3.12% (64/2051) 1 entry
ENSG00000134982 rectal adenocarcinoma conservative_inframe_deletion 60.51% (613/1013) 1 entry
ENSG00000134982 chronic lymphocytic leukemia sequence_alteration 0.8979% (8/891) 1 entry
ENSG00000134982 colon adenocarcinoma amino_acid_insertion 47.74% (1182/2476) 1 entry
ENSG00000134982 gastric adenocarcinoma sequence_alteration 4.46% (97/2175) 2 entries
ENSG00000134982 Gallbladder Adenocarcinoma sequence_alteration 3.017% (7/232) 1 entry
ENSG00000134982 Ileal Neuroendocrine Tumor G1 missense_variant 28.57% (2/7) 1 entry
ENSG00000134982 colonic neoplasm missense_variant 70.0% (14/20) 1 entry
ENSG00000134982 Gastric Neuroendocrine Tumor G1 missense_variant 17.65% (3/17) 1 entry
ENSG00000134982 breast ductal adenocarcinoma frameshift_variant 3.889% (73/1877) 4 entries
ENSG00000134982 squamous cell lung carcinoma frameshift_variant 2.317% (25/1079) 2 entries
ENSG00000134982 Appendix Adenocarcinoma missense_variant 1.431% (8/559) 1 entry
ENSG00000134982 esophageal adenocarcinoma missense_variant 5.928% (38/641) 3 entries
ENSG00000134982 hepatocellular carcinoma frameshift_variant 2.661% (29/1090) 3 entries
ENSG00000134982 pancreatic ductal adenocarcinoma frameshift_variant 3.12% (64/2051) 4 entries
ENSG00000134982 esophageal carcinoma missense_variant 1.363% (14/1027) 1 entry
ENSG00000134982 gastric intestinal type adenocarcinoma frameshift_variant 7.117% (20/281) 4 entries
ENSG00000134982 skin melanoma sequence_alteration 6.061% (76/1254) 2 entries
ENSG00000134982 small cell lung carcinoma frameshift_variant 3.025% (17/562) 2 entries
ENSG00000134982 Rectal Traditional Serrated Adenoma stop_gained 17.24% (5/29) 1 entry
ENSG00000134982 T-cell acute lymphoblastic leukemia sequence_alteration 2.658% (16/602) 2 entries
ENSG00000134982 esophageal squamous cell carcinoma missense_variant 2.583% (24/929) 8 entries
ENSG00000134982 lobular breast carcinoma missense_variant 2.318% (7/302) 1 entry
ENSG00000134982 colon adenocarcinoma conservative_inframe_deletion 47.74% (1182/2476) 1 entry
ENSG00000134982 colorectal adenocarcinoma amino_acid_insertion 49.18% (2322/4721) 1 entry
ENSG00000134982 esophageal adenocarcinoma stop_gained 5.928% (38/641) 4 entries
ENSG00000134982 brain glioblastoma sequence_alteration 1.845% (28/1518) 2 entries
ENSG00000134982 kidney Wilms tumor stop_gained 1.133% (4/353) 1 entry
ENSG00000134982 HER2 Positive Breast Carcinoma sequence_alteration 6.699% (14/209) 1 entry
ENSG00000134982 colon carcinoma stop_gained 25.0% (2/8) 1 entry
ENSG00000134982 prostate adenocarcinoma frameshift_variant 5.326% (120/2253) 4 entries
ENSG00000134982 bladder transitional cell carcinoma missense_variant 4.733% (31/655) 6 entries
ENSG00000134982 bile duct adenocarcinoma frameshift_variant 2.494% (20/802) 3 entries
ENSG00000134982 diffuse large B-cell lymphoma missense_variant 2.66% (10/376) 6 entries
ENSG00000134982 Rectal Tubular Adenoma missense_variant 62.96% (17/27) 1 entry
ENSG00000134982 hemangioblastoma sequence_alteration 8.571% (3/35) 1 entry
ENSG00000134982 Duodenal Adenocarcinoma missense_variant 18.29% (15/82) 3 entries
ENSG00000134982 Mixed Lobular and Ductal Breast Carcinoma stop_gained 1.449% (1/69) 1 entry
ENSG00000134982 Ovarian Microcystic Stromal Tumor missense_variant 100.0% (2/2) 1 entry
ENSG00000134982 adrenocortical adenoma sequence_alteration 3.704% (2/54) 1 entry
ENSG00000134982 epidermal appendage tumor missense_variant 14.29% (1/7) 1 entry
ENSG00000134982 Ameloblastic Carcinoma missense_variant 50.0% (1/2) 1 entry
ENSG00000134982 angioimmunoblastic T-cell lymphoma frameshift_variant 2.804% (3/107) 1 entry
ENSG00000134982 bladder transitional cell carcinoma frameshift_variant 4.733% (31/655) 1 entry
ENSG00000134982 bile duct adenocarcinoma sequence_alteration 2.494% (20/802) 1 entry
ENSG00000134982 Benign Thyroid Gland Neoplasm missense_variant 0.9259% (1/108) 1 entry
ENSG00000134982 diffuse large B-cell lymphoma stop_lost 2.66% (10/376) 1 entry
ENSG00000134982 adenoma of small intestine frameshift_variant 50.0% (1/2) 1 entry
ENSG00000134982 clear cell renal carcinoma stop_gained 0.9793% (17/1736) 1 entry
ENSG00000134982 Malignant Ovarian Mixed Epithelial Tumor sequence_alteration 16.67% (1/6) 1 entry
ENSG00000134982 Angiofibroma frameshift_variant 20.0% (1/5) 1 entry
ENSG00000134982 Eccrine Porocarcinoma missense_variant 6.25% (1/16) 1 entry
ENSG00000134982 Appendix Adenocarcinoma frameshift_variant 1.431% (8/559) 1 entry
ENSG00000134982 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma frameshift_variant 2.765% (12/434) 1 entry
ENSG00000134982 Adrenal Gland Neuroblastoma sequence_alteration 3.333% (2/60) 1 entry
ENSG00000134982 Colon Neuroendocrine Tumor G1 frameshift_variant 20.0% (1/5) 1 entry
ENSG00000134982 Pancreatic Acinar Cell Carcinoma stop_gained 7.609% (7/92) 1 entry
ENSG00000134982 head and neck squamous cell carcinoma sequence_alteration 0.6378% (5/784) 1 entry
ENSG00000134982 endometrial carcinoma sequence_alteration 5.0% (4/80) 1 entry
ENSG00000134982 Ovarian Microcystic Stromal Tumor frameshift_variant 100.0% (2/2) 1 entry
ENSG00000134982 tumor of duodenum missense_variant 16.67% (1/6) 1 entry
ENSG00000134982 Parathyroid Gland Carcinoma missense_variant 5.263% (1/19) 1 entry
ENSG00000134982 Ovarian Mixed Epithelial Tumor sequence_alteration 100.0% (1/1) 1 entry
ENSG00000134982 large cell medulloblastoma missense_variant 2.778% (1/36) 1 entry
ENSG00000134982 breast ductal adenocarcinoma conservative_inframe_deletion 3.889% (73/1877) 1 entry
ENSG00000134982 Ovarian Endometrioid Adenocarcinoma stop_gained 9.589% (7/73) 1 entry
ENSG00000134982 salivary gland adenoid cystic carcinoma frameshift_variant 3.125% (3/96) 1 entry
ENSG00000134982 desmoplastic fibroma stop_gained 50.0% (1/2) 1 entry
ENSG00000134982 myelodysplastic syndrome missense_variant 0.7692% (1/130) 1 entry
ENSG00000134982 neoplasm stop_gained 2.326% (1/43) 1 entry
ENSG00000134982 Invasive Breast Carcinoma missense_variant 2.857% (2/70) 1 entry
ENSG00000134982 alveolar rhabdomyosarcoma missense_variant 1.538% (1/65) 1 entry
ENSG00000134982 Vulvar Squamous Cell Carcinoma missense_variant 2.0% (1/50) 1 entry
ENSG00000134982 Ocular Sebaceous Carcinoma missense_variant 4.167% (1/24) 1 entry
ENSG00000134982 carcinoma frameshift_variant 25.0% (1/4) 1 entry
ENSG00000134982 papillary renal cell carcinoma stop_gained 0.7732% (3/388) 1 entry
ENSG00000134982 Adrenal Gland Neuroblastoma missense_variant 3.333% (2/60) 1 entry
ENSG00000134982 renal carcinoma missense_variant 5.0% (1/20) 1 entry
ENSG00000134982 follicular thyroid carcinoma frameshift_variant 3.704% (4/108) 1 entry
ENSG00000134982 solitary fibrous tumor missense_variant 3.226% (1/31) 1 entry
ENSG00000134982 large cell lung carcinoma stop_gained 1.887% (1/53) 1 entry
ENSG00000134982 angiosarcoma sequence_alteration 6.383% (3/47) 1 entry
ENSG00000134982 nasopharyngeal squamous cell carcinoma frameshift_variant 2.597% (8/308) 1 entry
ENSG00000134982 colon carcinoma missense_variant 25.0% (2/8) 1 entry
ENSG00000134982 carcinosarcoma stop_gained 33.33% (1/3) 1 entry
ENSG00000134982 Rectal Traditional Serrated Adenoma sequence_alteration 17.24% (5/29) 1 entry
ENSG00000134982 Poroma missense_variant 14.29% (1/7) 1 entry
ENSG00000134982 salivary gland adenoid cystic carcinoma stop_gained 3.125% (3/96) 1 entry
ENSG00000134982 desmoplastic small round cell tumor missense_variant 4.545% (1/22) 1 entry
ENSG00000134982 Primary Intraosseous Squamous Cell Carcinoma missense_variant 50.0% (1/2) 1 entry
ENSG00000134982 lung carcinoid tumor missense_variant 2.857% (1/35) 1 entry
ENSG00000134982 pharyngeal squamous cell carcinoma missense_variant 0.5848% (1/171) 1 entry
ENSG00000134982 T-cell acute lymphoblastic leukemia amino_acid_insertion 2.658% (16/602) 1 entry
ENSG00000134982 Testicular Yolk Sac Tumor stop_gained 11.11% (1/9) 1 entry
ENSG00000134982 Kidney Oncocytoma missense_variant 2.326% (1/43) 1 entry
ENSG00000134982 Thymoma stop_gained 0.7194% (1/139) 1 entry
ENSG00000134982 adrenocortical adenoma frameshift_variant 3.704% (2/54) 1 entry
ENSG00000134982 desmoplastic medulloblastoma stop_gained 2.564% (1/39) 1 entry
ENSG00000134982 Breast Carcinoma by Gene Expression Profile frameshift_variant 4.386% (5/114) 1 entry
ENSG00000134982 anaplastic astrocytoma stop_gained 2.516% (4/159) 1 entry
ENSG00000134982 central nervous system primitive neuroectodermal neoplasm stop_gained 0.9831% (7/712) 1 entry
ENSG00000134982 Pleural Biphasic Mesothelioma stop_gained 1.333% (1/75) 1 entry
ENSG00000134982 astrocytoma missense_variant 16.67% (1/6) 1 entry
ENSG00000134982 villous adenoma of colon frameshift_variant 11.11% (1/9) 1 entry
ENSG00000134982 bronchoalveolar adenocarcinoma stop_gained 4.545% (1/22) 1 entry
ENSG00000134982 metaplastic breast carcinoma frameshift_variant 4.795% (7/146) 1 entry
ENSG00000134982 thyroid carcinoma frameshift_variant 1.606% (15/934) 1 entry
ENSG00000134982 neuroendocrine carcinoma missense_variant 14.29% (1/7) 1 entry
ENSG00000134982 Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor frameshift_variant 2.941% (1/34) 1 entry
ENSG00000134982 Kidney Angiomyolipoma missense_variant 12.5% (1/8) 1 entry
ENSG00000134982 Ovarian Mixed Epithelial Tumor frameshift_variant 100.0% (1/1) 1 entry
ENSG00000134982 oral squamous cell carcinoma stop_gained 2.477% (8/323) 1 entry
ENSG00000134982 Bladder Adenocarcinoma frameshift_variant 13.64% (3/22) 1 entry
ENSG00000134982 Follicular Variant Thyroid Gland Papillary Carcinoma missense_variant 2.703% (1/37) 1 entry
ENSG00000134982 HER2 Positive Breast Carcinoma stop_gained 6.699% (14/209) 1 entry
ENSG00000134982 salivary gland adenoid cystic carcinoma missense_variant 3.125% (3/96) 1 entry
ENSG00000134982 Rhabdoid Meningioma missense_variant 100.0% (1/1) 1 entry
ENSG00000134982 Chordoma missense_variant 2.857% (1/35) 1 entry
ENSG00000134982 Gastric Neuroendocrine Tumor G1 frameshift_variant 17.65% (3/17) 1 entry
ENSG00000134982 medulloblastoma missense_variant 4.167% (1/24) 1 entry
ENSG00000134982 B-cell acute lymphoblastic leukemia missense_variant 0.8929% (1/112) 1 entry
ENSG00000134982 non-small cell lung carcinoma conservative_inframe_deletion 1.312% (10/762) 1 entry
ENSG00000134982 brain glioblastoma conservative_inframe_deletion 1.845% (28/1518) 1 entry
ENSG00000134982 Gastrointestinal stromal tumor missense_variant 0.6579% (1/152) 1 entry
ENSG00000134982 rectal neoplasm missense_variant 80.0% (4/5) 1 entry
ENSG00000134982 lobular breast carcinoma stop_gained 2.318% (7/302) 1 entry
ENSG00000134982 Prostate Small Cell Carcinoma sequence_alteration 15.79% (3/19) 1 entry
ENSG00000134982 glioma frameshift_variant 0.3333% (2/600) 1 entry
ENSG00000134982 Gallbladder Adenocarcinoma frameshift_variant 3.017% (7/232) 1 entry
ENSG00000134982 head and neck squamous cell carcinoma stop_gained 0.6378% (5/784) 1 entry
ENSG00000134982 central nervous system primitive neuroectodermal neoplasm conservative_inframe_deletion 0.9831% (7/712) 1 entry
ENSG00000134982 esophageal carcinoma stop_gained 1.363% (14/1027) 1 entry
ENSG00000134982 Uterine Carcinosarcoma conservative_inframe_deletion 1.087% (2/184) 1 entry
ENSG00000134982 leiomyosarcoma missense_variant 0.8475% (1/118) 1 entry
ENSG00000134982 Liver Cavernous Hemangioma missense_variant 16.67% (1/6) 1 entry
ENSG00000134982 T-cell acute lymphoblastic leukemia conservative_inframe_deletion 2.658% (16/602) 1 entry
ENSG00000134982 Crohn's disease missense_variant 7.692% (1/13) 1 entry
ENSG00000134982 basal cell carcinoma stop_gained 9.639% (8/83) 1 entry
ENSG00000134982 Dysplasia in Ulcerative Colitis stop_gained 37.5% (3/8) 1 entry
ENSG00000134982 liposarcoma missense_variant 4.167% (1/24) 1 entry
ENSG00000134982 undifferentiated pleomorphic sarcoma stop_gained 4.167% (3/72) 1 entry
ENSG00000134982 endometrial carcinoma frameshift_variant 5.0% (4/80) 1 entry
ENSG00000134982 Thymic Carcinoma missense_variant 6.667% (1/15) 1 entry
ENSG00000134982 angioimmunoblastic T-cell lymphoma conservative_inframe_deletion 2.804% (3/107) 1 entry
ENSG00000134982 mucosal melanoma stop_gained 4.286% (3/70) 1 entry
ENSG00000134982 Merkel cell skin cancer stop_gained 3.509% (6/171) 1 entry
ENSG00000134982 salivary gland squamous cell carcinoma missense_variant 50.0% (1/2) 1 entry
ENSG00000134982 ovarian serous adenocarcinoma stop_gained 1.396% (13/931) 1 entry
ENSG00000134982 Signet Ring Cell Gastric Adenocarcinoma missense_variant 7.895% (3/38) 1 entry
ENSG00000134982 malignant epithelioid mesothelioma missense_variant 100.0% (1/1) 1 entry
ENSG00000134982 ossifying fibroma missense_variant 12.5% (1/8) 1 entry
ENSG00000134982 esophageal squamous cell carcinoma frameshift_variant 2.583% (24/929) 1 entry
ENSG00000134982 prostate adenocarcinoma conservative_inframe_deletion 5.326% (120/2253) 1 entry
ENSG00000134982 Appendix Goblet Cell Carcinoid stop_gained 4.762% (1/21) 1 entry
ENSG00000134982 Hepatoblastoma frameshift_variant 23.08% (9/39) 1 entry
ENSG00000134982 brain glioblastoma stop_gained 1.845% (28/1518) 1 entry
ENSG00000134982 Anal Squamous Cell Carcinoma missense_variant 1.205% (1/83) 1 entry
ENSG00000134982 ependymoma missense_variant 1.053% (1/95) 1 entry
ENSG00000134982 gastric adenocarcinoma conservative_inframe_deletion 4.46% (97/2175) 1 entry
ENSG00000134982 non-small cell lung carcinoma stop_gained 1.312% (10/762) 1 entry
ENSG00000134982 central nervous system primitive neuroectodermal neoplasm frameshift_variant 0.9831% (7/712) 1 entry
ENSG00000134982 Invasive Breast Carcinoma stop_gained 2.857% (2/70) 1 entry
ENSG00000134982 Uterine Carcinosarcoma frameshift_variant 1.087% (2/184) 1 entry
ENSG00000134982 hepatocellular adenoma frameshift_variant 8.333% (1/12) 1 entry
ENSG00000134982 Cortisol-Producing Adrenal Cortex Adenoma missense_variant 1.575% (2/127) 1 entry
ENSG00000134982 kidney Wilms tumor frameshift_variant 1.133% (4/353) 1 entry
ENSG00000134982 Parotid Gland Squamous Cell Carcinoma missense_variant 9.091% (1/11) 1 entry
ENSG00000134982 alveolar soft part sarcoma missense_variant 4.545% (1/22) 1 entry
ENSG00000134982 multiple myeloma frameshift_variant 0.5587% (1/179) 1 entry
ENSG00000134982 Pleural Epithelioid Mesothelioma missense_variant 1.442% (3/208) 1 entry
ENSG00000134982 lung adenocarcinoma amino_acid_insertion 3.746% (121/3230) 1 entry
ENSG00000134982 angioimmunoblastic T-cell lymphoma missense_variant 2.804% (3/107) 1 entry
ENSG00000134982 Cortisol-Producing Adrenal Cortex Adenoma stop_gained 1.575% (2/127) 1 entry
ENSG00000134982 Epidermal Inclusion Cyst sequence_alteration 50.0% (1/2) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000134982 STAD 0.018 high
ENSG00000134982 THCA 0.025 high
ENSG00000134982 ACC 0.049 low
ENSG00000134982 LGG 0.013 high
ENSG00000134982 HNSC 0.0066 low
ENSG00000134982 KIRP 0.033 high
ENSG00000134982 KICH 0.0032 high
ENSG00000134982 LUAD 0.049 high
ENSG00000134982 BRCA 0.0013 high
ENSG00000134982 COAD 0.049 low
ENSG00000134982 UCS 0.032 high
ENSG00000134982 OV 0.0044 high
ENSG00000134982 BLCA 0.0042 high
ENSG00000134982 GBM 0.032 low
ENSG00000134982 SKCM 0.0069 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000134982 LUSC Del 1.199953 0.073041 0.399613 0.772455
ENSG00000134982 LAML Del 5.363882 0.082191 0.793419 0.083770
ENSG00000134982 LUAD Del 2.558982 0.072806 0.345789 0.399225
ENSG00000134982 ACC Amp 0.754856 0.252744 1.281818 0.655556
ENSG00000134982 READ Del 5.438590 0.160757 0.456605 0.351515
ENSG00000134982 COAD Del 16.549391 0.149074 0.461954 0.286031
ENSG00000134982 SKCM Del 1.322898 0.076700 0.466339 0.297003
ENSG00000134982 BLCA Del 0.706488 0.076688 0.389276 0.480392
ENSG00000134982 STAD Del 8.757183 0.137479 0.400770 0.367347
ENSG00000134982 PRAD Del 5.542185 0.119268 0.532581 0.136179
ENSG00000134982 KIRC Amp 22.232827 0.169586 0.514645 0.520833
ENSG00000134982 OV Del 17.477771 0.363314 0.616244 0.566494