Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
MED13L |
Breast Cancer | p143_p3 |
Chr12:116422046:G>C |
Private mutation |
MED13L |
Colorectal Cancer | p034_MSU2 |
Chr12:116549253:C>T |
Trunk mutation |
MED13L |
Colorectal Cancer | p040_case3 |
Chr12:116434879:T>G |
Private mutation |
MED13L |
Colorectal Cancer | p040_case9 |
Chr12:116675365:C>T |
Trunk mutation |
MED13L |
Esophageal Squamous Cell Carcinoma | p008_ESCC10 |
p.V1111I |
Trunk mutation |
MED13L |
Esophageal Squamous Cell Carcinoma | p124_ESCC030 |
p.L606V |
Private mutation |
MED13L |
Esophageal Squamous Cell Carcinoma | p128_P13 |
Chr12:116434479:C>T |
Private mutation |
MED13L |
Esophageal Squamous Cell Carcinoma | p128_SP14 |
Chr12:116429072:C>A |
Private mutation |
MED13L |
Esophageal Squamous Cell Carcinoma | p128_SP27 |
Chr12:116675493:C>T |
Private mutation |
MED13L |
Gastric Carcinoma | p106_GC14 |
p.S923S |
Private mutation |
MED13L |
Anaplastic Astrocytoma | p070_HGG1 |
Chr12:116714287:G>A |
Private mutation |
MED13L |
Glioma | p168_P18 |
p.L1109L |
Private mutation |
MED13L |
Hepatocellular Carcinoma | p061_P03 |
Chr12:116425012:T>A |
Trunk mutation |
MED13L |
Hepatocellular Carcinoma | p151_HCC8031 |
Chr12:116429330:C>T |
Branch mutation |
MED13L |
Hepatocellular Carcinoma | p157_p4 |
p.A166S |
Branch mutation |
MED13L |
Medulloblastoma | p072_MB6 |
Chr12:116434117:A>G |
Branch mutation |
MED13L |
Medulloblastoma | p072_MB6 |
Chr12:116457493:G>A |
Branch mutation |
MED13L |
Melanoma | p043_C |
p.P640L |
Trunk mutation |
MED13L |
Melanoma | p043_C |
p.P417T |
Trunk mutation |
MED13L |
Melanoma | p043_F |
p.E711K |
Trunk mutation |
MED13L |
Urothelial Carcinoma | p031_WCM088 |
p.V1004F |
Private mutation |
MED13L |
Urothelial Carcinoma | p031_WCM117 |
p.Q103K |
Private mutation |
MED13L |
Urothelial Carcinoma | p031_WCM259 |
p.V712V |
Trunk mutation |