Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
---|---|---|---|---|
RAP1GAP2 | Colorectal Cancer | p034_MSU1 | Chr17:2923790:C>T | Trunk mutation |
RAP1GAP2 | Colorectal Cancer | p034_MSU4 | Chr17:2868852:T>G | Private mutation |
RAP1GAP2 | Colorectal Cancer | p040_case3 | Chr17:2923885:C>T | Branch mutation |
RAP1GAP2 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.S182F | Private mutation |
RAP1GAP2 | Gastric Adenocarcinoma | p011_MSS3 | p.S668S | Private mutation |
RAP1GAP2 | Glioma | p020_Patient04 | p.S446L | Private mutation |
RAP1GAP2 | Glioblastoma | p113_case07 | p.E537K | Private mutation |
RAP1GAP2 | Glioma | p168_P04 | p.S446L | Private mutation |
RAP1GAP2 | Glioma | p168_P18 | p.L349L | Private mutation |
RAP1GAP2 | Intrahepatic Cholangiocarcinoma | p080_ICC1370 | p.V406I | Trunk mutation |
RAP1GAP2 | Ovarian Cancer | p144_AOCS167 | p.R485H | Private mutation |