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).
- 17:09, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:08, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Von Hippel-Lindau syndrome (VHL) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:08, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Hyperparathyroidism jaw tumour syndrome (CDC73) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:08, 29 December 2024 Jennelleh talk contribs created page GTS5:Hyperparathyroidism jaw tumour syndrome (CDC73) (Created page with "?")
- 17:08, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Hyperparathyroidism jaw tumour syndrome (CDC73) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:08, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Familial chordoma (TBXT) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:07, 29 December 2024 Jennelleh talk contribs created page GTS5:Familial chordoma (TBXT) (Created page with "?")
- 17:07, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Familial chordoma (TBXT) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:07, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Birt-Hogg-Dube syndrome (FLCN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:07, 29 December 2024 Jennelleh talk contribs created page GTS5:Birt-Hogg-Dube syndrome (FLCN) (Created page with "?")
- 17:07, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Birt-Hogg-Dube syndrome (FLCN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:07, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:MAFA-related familial insulinomatosis (MAFA) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:07, 29 December 2024 Jennelleh talk contribs created page GTS5:MAFA-related familial insulinomatosis (MAFA) (Created page with "?")
- 17:07, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:MAFA-related familial insulinomatosis (MAFA) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:07, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Multiple endocrine neoplasia type 5, MAX related tumours (MAX) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:07, 29 December 2024 Jennelleh talk contribs created page GTS5:Multiple endocrine neoplasia type 5, MAX related tumours (MAX) (Created page with "?")
- 17:07, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Multiple endocrine neoplasia type 5, MAX related tumours (MAX) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:06, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Activated Phosphatidylinositol-3-OH kinase δ Syndrome - APDS (PIK3CD) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:06, 29 December 2024 Jennelleh talk contribs created page GTS5:Activated Phosphatidylinositol-3-OH kinase δ Syndrome - APDS (PIK3CD) (Created page with "?")
- 17:06, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Activated Phosphatidylinositol-3-OH kinase δ Syndrome - APDS (PIK3CD) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:06, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:PTEN hamartoma tumour syndrome (PTEN) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:06, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Tuberous sclerosis (TSC1, TSC1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:06, 29 December 2024 Jennelleh talk contribs created page GTS5:Tuberous sclerosis (TSC1, TSC1) (Created page with "?")
- 17:06, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Tuberous sclerosis (TSC1, TSC1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:06, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Brooke-Spiegler syndrome (CYLD) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:06, 29 December 2024 Jennelleh talk contribs created page GTS5:Brooke-Spiegler syndrome (CYLD) (Created page with "?")
- 17:06, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Brooke-Spiegler syndrome (CYLD) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:05, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Osteochondromatosis (EXT1, EXT2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:05, 29 December 2024 Jennelleh talk contribs created page GTS5:Osteochondromatosis (EXT1, EXT2) (Created page with "?")
- 17:05, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Osteochondromatosis (EXT1, EXT2) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:05, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:ELP1-related medulloblastoma predisposition syndrome(ELP1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:05, 29 December 2024 Jennelleh talk contribs created page GTS5:ELP1-related medulloblastoma predisposition syndrome(ELP1) (Created page with "?")
- 17:05, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:ELP1-related medulloblastoma predisposition syndrome(ELP1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:05, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:SMO-related Curry-Jones syndrome (SMO) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:05, 29 December 2024 Jennelleh talk contribs created page GTS5:SMO-related Curry-Jones syndrome (SMO) (Created page with "?")
- 17:05, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:SMO-related Curry-Jones syndrome (SMO) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:04, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:04, 29 December 2024 Jennelleh talk contribs created page GTS5:Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161) (Created page with "?")
- 17:04, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:04, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Hereditary mixed polyposis syndrome (GREM1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:04, 29 December 2024 Jennelleh talk contribs created page GTS5:Hereditary mixed polyposis syndrome (GREM1) (Created page with "?")
- 17:04, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:Hereditary mixed polyposis syndrome (GREM1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:03, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Hereditary gastric and breast cancer syndrome (CDH1, CTNNA1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:03, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Peutz-Jeghers syndrome (STK11) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:03, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Multiple endocrine neoplasia type 1 (MEN1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:02, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:WAGR syndrome (WT1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:02, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:WT1 related tumour predisposition syndrome (WT1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:02, 29 December 2024 Jennelleh talk contribs created page GTS5:WT1 related tumour predisposition syndrome (WT1) (Created page with "?")
- 17:02, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-ia" on GTS5:WT1 related tumour predisposition syndrome (WT1) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])
- 17:01, 29 December 2024 Jennelleh talk contribs performed unknown action "review/approve-a" on GTS5:Serrated polyposis (RNF43) ([Accuracy: Spot checked, Depth: Basic, Readability: Acceptable])