Entries searched:
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
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