Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
CNTNAP1 |
Breast Cancer | p143_p3 |
Chr17:40839038:C>T |
Private mutation |
CNTNAP1 |
Colorectal Cancer | p034_MSU4 |
Chr17:40848084:G>A |
Private mutation |
CNTNAP1 |
Colorectal Cancer | p040_case9 |
Chr17:40841011:G>A |
Private mutation |
CNTNAP1 |
Colorectal Cancer | p104_UC03 |
p.L823P |
Branch mutation |
CNTNAP1 |
Colorectal Cancer | p147_a20 |
p.R1058H |
Private mutation |
CNTNAP1 |
Esophageal Squamous Cell Carcinoma | p124_ESCC026 |
p.P1060P |
Trunk mutation |
CNTNAP1 |
Esophageal Squamous Cell Carcinoma | p128_P21 |
Chr17:40847630:G>T |
Private mutation |
CNTNAP1 |
Esophageal Squamous Cell Carcinoma | p139_EC1020 |
p.R973C |
Private mutation |
CNTNAP1 |
Esophageal Squamous Cell Carcinoma | p139_EC1110 |
p.R331C |
Private mutation |
CNTNAP1 |
Gastric Adenocarcinoma | p011_MSI-H1 |
p.E226K |
Trunk mutation |
CNTNAP1 |
Gastric Carcinoma | p106_GC09 |
p.L394R |
Private mutation |
CNTNAP1 |
Glioblastoma | p113_case31 |
p.T48Cfs*44 |
Private mutation |
CNTNAP1 |
Glioblastoma | p113_case31 |
p.A49Efs*42 |
Private mutation |
CNTNAP1 |
Melanoma | p043_G |
p.E699* |
Trunk mutation |
CNTNAP1 |
Melanoma | p043_H |
p.D552N |
Private mutation |
CNTNAP1 |
Melanoma | p135_p01 |
Chr17:40843161:A>G |
Private mutation |
CNTNAP1 |
Urothelial Carcinoma | p031_WCM088 |
p.T413M |
Private mutation |