| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| DIP2B | Bladder Cancer | p084_p1 | - | Private mutation |
| DIP2B | Breast Cancer | p091_A7 | p.I1057T | Branch mutation |
| DIP2B | Breast Cancer | p111_p8-82 | p.G1366A | Private mutation |
| DIP2B | Breast Cancer | p123_case7 | p.S1489T | Trunk mutation |
| DIP2B | Colorectal Cancer | p001_PCRC05 | Chr12:51080371:A>G | Private mutation |
| DIP2B | Colorectal Cancer | p034_MSU2 | Chr12:51102285:G>A | Trunk mutation |
| DIP2B | Colorectal Cancer | p034_MSU2 | Chr12:51122405:C>T | Private mutation |
| DIP2B | Colorectal Cancer | p104_UC02 | p.L976M | Private mutation |
| DIP2B | Colorectal Cancer | p155_p335 | p.S53I | Private mutation |
| DIP2B | Esophageal Squamous Cell Carcinoma | p008_ESCC05 | p.Q1143X | Private mutation |
| DIP2B | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.S217C | Branch mutation |
| DIP2B | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.F1302L | Branch mutation |
| DIP2B | Esophageal Squamous Cell Carcinoma | p128_SP30 | Chr12:51065098:C>A | Trunk mutation |
| DIP2B | Esophageal Squamous Cell Carcinoma | p139_EC1125 | p.G1273R | Private mutation |
| DIP2B | Anaplastic Astrocytoma | p070_HGG1 | Chr12:51084850:G>T | Private mutation |
| DIP2B | Glioma | p168_P18 | p.K293K | Private mutation |
| DIP2B | Hepatocellular Carcinoma | p061_P07 | Chr12:51122354:T>C | Branch mutation |
| DIP2B | Hepatocellular Carcinoma | p061_P08 | Chr12:51065076:A>G | Private mutation |
| DIP2B | Lung Cancer | p028_RJLC2 | p.A218V | Private mutation |
| DIP2B | Melanoma | p043_H | p.P244L | Private mutation |
| DIP2B | Ovarian Serous Carcinomas | p006_OSC3 | c.1934-1G>C | Private mutation |
| DIP2B | Ovarian Cancer | p052_Case3 | - | Trunk mutation |
| DIP2B | Ovarian Cancer | p144_AOCS167 | p.V197G | Trunk mutation |
| DIP2B | Pancreatic Cancer | p054_Pa01 | - | Trunk mutation |
| DIP2B | Syndromic Neuroendocrine Carcinoma | p127_C4 | c.3927N>A | Private mutation |
| DIP2B | Urothelial Carcinoma | p031_WCM249 | p.V1283L | Private mutation |