Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
SON |
Breast Cancer | p123_case6 |
p.E2239K |
Trunk mutation |
SON |
Breast Cancer | p123_case6 |
p.D2243N |
Trunk mutation |
SON |
Breast Cancer | p143_p3 |
Chr21:34926272:G>A |
Private mutation |
SON |
Breast Cancer | p143_p5 |
Chr21:34925700:T>G |
Branch mutation |
SON |
Osteosarcoma | p102_OS07 |
Chr21:34926227:G>C |
Private mutation |
SON |
Osteosarcoma | p112_OS1101 |
p.T2051S |
Private mutation |
SON |
Colorectal Cancer | p004_CRC_A02 |
Chr21:34924818:C>T |
Private mutation |
SON |
Colorectal Cancer | p034_MSU1 |
Chr21:34926767:C>T |
Trunk mutation |
SON |
Colorectal Cancer | p147_a08 |
p.E126K |
Private mutation |
SON |
Esophageal Squamous Cell Carcinoma | p124_ESCC014 |
p.K323fs |
Private mutation |
SON |
Esophageal Squamous Cell Carcinoma | p124_ESCC023 |
p.M1284V |
Trunk mutation |
SON |
Esophageal Squamous Cell Carcinoma | p128_P02 |
Chr21:34932280:A>G |
Branch mutation |
SON |
Esophageal Squamous Cell Carcinoma | p128_P09 |
Chr21:34924802:G>A |
Branch mutation |
SON |
Esophageal Squamous Cell Carcinoma | p128_SP02 |
Chr21:34932280:A>G |
Trunk mutation |
SON |
Gastric Adenocarcinoma | p011_MSS2 |
p.P414A |
Trunk mutation |
SON |
Glioblastoma | p113_case07 |
p.T900N |
Trunk mutation |
SON |
Glioblastoma | p113_case07 |
p.E1324K |
Private mutation |
SON |
Glioblastoma | p113_case08 |
p.R1122H |
Private mutation |
SON |
Glioblastoma | p113_case08 |
p.M1431I |
Private mutation |
SON |
Glioma | p168_P01 |
p.P2197S |
Private mutation |
SON |
Glioma | p168_P18 |
p.D772Y |
Private mutation |
SON |
Glioma | p168_P18 |
p.D2296N |
Private mutation |
SON |
Hepatocellular Carcinoma | p061_P10 |
Chr21:34924628:CGCTCTATGATGTCAGCCTACGAG>* |
Trunk mutation |
SON |
Non-Small Cell Lung Cancer | p107_P004 |
p.A496V |
Private mutation |
SON |
Medulloblastoma | p072_MB6 |
Chr21:34941275:A>T |
Private mutation |
SON |
Melanoma | p043_A |
p.P2197S |
Trunk mutation |
SON |
Melanoma | p043_D |
p.L1376M |
Trunk mutation |
SON |
Ovarian Cancer | p144_AOCS139 |
p.S2247S |
Private mutation |
SON |
Urothelial Carcinoma | p031_WCM077 |
p.V2198L |
Private mutation |