Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
ANKRD12 |
Breast Cancer | p123_case4 |
p.D1992H |
Branch mutation |
ANKRD12 |
Breast Cancer | p143_p2 |
Chr18:9258597:G>C |
Private mutation |
ANKRD12 |
Osteosarcoma | p112_OS1107 |
E13_UTR_3 |
Trunk mutation |
ANKRD12 |
Colorectal Cancer | p001_PCRC12 |
Chr18:9257882:T>C |
Branch mutation |
ANKRD12 |
Colorectal Cancer | p034_MSU2 |
Chr18:9281058:C>T |
Trunk mutation |
ANKRD12 |
Colorectal Cancer | p040_case9 |
Chr18:9255944:T>G |
Private mutation |
ANKRD12 |
Colorectal Cancer | p040_case9 |
Chr18:9255948:A>- |
Private mutation |
ANKRD12 |
Colorectal Cancer | p147_a13 |
p.E979G |
Private mutation |
ANKRD12 |
Colorectal Cancer | p155_p496 |
p.V1220M |
Private mutation |
ANKRD12 |
Colorectal Cancer | p155_p496 |
p.V1220G |
Private mutation |
ANKRD12 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.D1972N |
Branch mutation |
ANKRD12 |
Esophageal Squamous Cell Carcinoma | p124_ESCC034 |
p.D365H |
Branch mutation |
ANKRD12 |
Esophageal Squamous Cell Carcinoma | p139_EC0966 |
p.Q1494H |
Trunk mutation |
ANKRD12 |
Esophageal Squamous Cell Carcinoma | p139_EC0990 |
p.E1283Q |
Private mutation |
ANKRD12 |
Esophageal Squamous Cell Carcinoma | p139_EC1111 |
p.H1296fs |
Branch mutation |
ANKRD12 |
Gastric Adenocarcinoma | p011_MSS1 |
p.H546D |
Trunk mutation |
ANKRD12 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.S818N |
Trunk mutation |
ANKRD12 |
Gastric Carcinoma | p106_GC08 |
p.T1319S |
Trunk mutation |
ANKRD12 |
Hepatocellular Carcinoma | p061_P08 |
Chr18:9257826:A>G |
Branch mutation |
ANKRD12 |
Hepatocellular Carcinoma | p157_p1 |
p.D1513N |
Private mutation |
ANKRD12 |
Non-Small Cell Lung Cancer | p107_P016 |
p.K1017_K1019[2>1] |
Private mutation |
ANKRD12 |
Medulloblastoma | p072_MB6 |
Chr18:9211444:C>A |
Private mutation |
ANKRD12 |
Melanoma | p043_B |
p.S1573L |
Trunk mutation |
ANKRD12 |
Melanoma | p043_H |
p.G315E |
Private mutation |
ANKRD12 |
Prostate Cancer | p119_CAP004 |
p.I238del |
Private mutation |
ANKRD12 |
Prostate Cancer | p164_P1 |
p.K883R |
Private mutation |