Main public logs

Combined display of all available logs of Compendium of Cancer Genome Aberrations. You can narrow down the view by selecting a log type, the username (case-sensitive), or the affected page (also case-sensitive).

• 17:26, 29 December 2024 Jennelleh talk contribs created page GTS5:Nijmegen breakage syndrome (NBN) (Created page with "?")
• 17:26, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Nijmegen breakage syndrome (NBN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:26, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:CHEK2-related hereditary (breast) cancer predisposition syndrome (CHEK2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:25, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Ataxia-telangiectasia syndrome (ATM) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:25, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Xeroderma Pigmentosum ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:25, 29 December 2024 Jennelleh talk contribs created page GTS5:Xeroderma Pigmentosum (Created page with "?")
• 17:25, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Xeroderma Pigmentosum ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:25, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:MBD4-associated neoplasia syndrome (MBD4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:25, 29 December 2024 Jennelleh talk contribs created page GTS5:MBD4-associated neoplasia syndrome (MBD4) (Created page with "?")
• 17:25, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:MBD4-associated neoplasia syndrome (MBD4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:25, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:NTHL1-related tumour syndrome (NTHL1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:24, 29 December 2024 Jennelleh talk contribs created page GTS5:NTHL1-related tumour syndrome (NTHL1) (Created page with "?")
• 17:24, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:NTHL1-related tumour syndrome (NTHL1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:24, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:MUTYH-associated polyposis (MUTYH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:24, 29 December 2024 Jennelleh talk contribs created page GTS5:MUTYH-associated polyposis (MUTYH) (Created page with "?")
• 17:24, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:MUTYH-associated polyposis (MUTYH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:23, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Fanconi anaemia (FANC genes) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:23, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:RAD51-related cancer predisposition syndrome (RAD51C, RAD51D) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:22, 29 December 2024 Jennelleh talk contribs created page GTS5:RAD51-related cancer predisposition syndrome (RAD51C, RAD51D) (Created page with "?")
• 17:22, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:RAD51-related cancer predisposition syndrome (RAD51C, RAD51D) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:19, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:PALB2-related cancer predisposition syndrome (PALB2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:18, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:BRCA-related cancer predisposition syndrome (BRCA1, BRCA2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:17, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:16, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve" on GTS5:Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:13, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:13, 29 December 2024 Jennelleh talk contribs created page GTS5:Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6) (Created page with "?")
• 17:13, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:13, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Lynch Syndrome (MLH1, PMS2, MSH2, MSH6) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:12, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Autoimmune lymphoproliferative syndrome (FAS) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:12, 29 December 2024 Jennelleh talk contribs created page GTS5:Autoimmune lymphoproliferative syndrome (FAS) (Created page with "?")
• 17:12, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Autoimmune lymphoproliferative syndrome (FAS) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:12, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:CDK4-related melanoma predisposition syndrome (CDK4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:12, 29 December 2024 Jennelleh talk contribs created page GTS5:CDK4-related melanoma predisposition syndrome (CDK4) (Created page with "?")
• 17:12, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:CDK4-related melanoma predisposition syndrome (CDK4) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:11, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:CDKN2A-related tumour predisposition syndrome (CDKN2A) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:11, 29 December 2024 Jennelleh talk contribs created page GTS5:CDKN2A-related tumour predisposition syndrome (CDKN2A) (Created page with "?")
• 17:11, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:CDKN2A-related tumour predisposition syndrome (CDKN2A) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:11, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Multiple endocrine neoplasia type 4 (CDKN1B) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:11, 29 December 2024 Jennelleh talk contribs created page GTS5:Multiple endocrine neoplasia type 4 (CDKN1B) (Created page with "?")
• 17:11, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Multiple endocrine neoplasia type 4 (CDKN1B) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:11, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Retinoblastoma syndrome (RB1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:11, 29 December 2024 Jennelleh talk contribs created page GTS5:Retinoblastoma syndrome (RB1) (Created page with "?")
• 17:11, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Retinoblastoma syndrome (RB1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:10, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Li-Fraumeni syndrome (TP53) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:09, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Hereditary tyrosinaemia type 1 (FAH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:09, 29 December 2024 Jennelleh talk contribs created page GTS5:Hereditary tyrosinaemia type 1 (FAH) (Created page with "?")
• 17:09, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Hereditary tyrosinaemia type 1 (FAH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:09, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
• 17:09, 29 December 2024 Jennelleh talk contribs created page GTS5:Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH) (Created page with "?")
• 17:09, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])