Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
EMILIN2 |
Breast Cancer | p123_case8 |
p.K689K |
Branch mutation |
EMILIN2 |
Osteosarcoma | p102_OS01 |
Chr18:2891720:A>C |
Private mutation |
EMILIN2 |
Colorectal Cancer | p034_MSU1 |
Chr18:2891855:G>A |
Trunk mutation |
EMILIN2 |
Colorectal Cancer | p034_MSU3 |
Chr18:2909759:C>T |
Trunk mutation |
EMILIN2 |
Esophageal Squamous Cell Carcinoma | p008_ESCC06 |
p.A49V |
Trunk mutation |
EMILIN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC009 |
p.R436C |
Branch mutation |
EMILIN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC027 |
p.Q678H |
Private mutation |
EMILIN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC043 |
p.D278Y |
Branch mutation |
EMILIN2 |
Mixed Adenoneuroendocrine Carcinoma | p125_M9 |
Chr18:2892369:C>T |
Trunk mutation |
EMILIN2 |
Esophageal Squamous Cell Carcinoma | p128_SP05 |
Chr18:2891557:G>A |
Trunk mutation |
EMILIN2 |
Esophageal Squamous Cell Carcinoma | p139_EC1071 |
p.R476Q |
Trunk mutation |
EMILIN2 |
Esophageal Squamous Cell Carcinoma | p139_EC1110 |
p.T692M |
Private mutation |
EMILIN2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.R574R |
Trunk mutation |
EMILIN2 |
Gastric Carcinoma | p106_GC04 |
p.A70T |
Private mutation |
EMILIN2 |
Hepatocellular Carcinoma | p151_HCC6952 |
Chr18:2892353:A>T |
Trunk mutation |
EMILIN2 |
Urothelial Carcinoma | p142_p13 |
- |
Private mutation |