| 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 |