Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
SCNN1G Breast Cancer p131_case4 p.I384T Trunk mutation
SCNN1G Osteosarcoma p112_OS1107 E13_UTR_3 Private mutation
SCNN1G Colorectal Cancer p001_PCRC01 Chr16:23200923:C>T Private mutation
SCNN1G Colorectal Cancer p001_PCRC12 Chr16:23226700:C>T Branch mutation
SCNN1G Colorectal Cancer p104_CD01 p.S476S Private mutation
SCNN1G Colorectal Cancer p155_p495 p.I186M Private mutation
SCNN1G Esophageal Squamous Cell Carcinoma p124_ESCC007 p.V544A Trunk mutation
SCNN1G Esophageal Squamous Cell Carcinoma p124_ESCC018 p.R90Q Trunk mutation
SCNN1G Esophageal Squamous Cell Carcinoma p128_P24 Chr16:23200793:C>T Private mutation
SCNN1G Esophageal Squamous Cell Carcinoma p128_SP20 Chr16:23224431:G>T Private mutation
SCNN1G Gastric Carcinoma p106_GC15 p.A350A Private mutation
SCNN1G Hepato-Cholangiocarcinoma p078_p6 p.E120K Trunk mutation
SCNN1G Medulloblastoma p072_MB6 Chr16:23224652:T>C Trunk mutation
SCNN1G Melanoma p043_C p.P580L Trunk mutation
SCNN1G Pancreatic Cancer p054_Pa05 - Trunk mutation
SCNN1G Renal Cancer p018_patient2 Chr16:23223474:T>A Trunk mutation
SCNN1G Clear Cell Renal Cell Carcinoma p019_EV002 Chr16:23223474:Splice site Trunk mutation
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