Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
HMGCS2 Esophageal Squamous Cell Carcinoma p139_EC1155 p.R464H Private mutation
HMGCS2 Gastric Carcinoma p106_GC15 p.C227X Private mutation
HMGCS2 Hepatocellular Carcinoma p158_pa Chr1:120306816:T>C Branch mutation
HMGCS2 Melanoma p043_F p.E20K Trunk mutation
HMGCS2 Melanoma p043_H p.P289L Private mutation
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