| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| NUP214 | Colorectal Cancer | p004_CRC_A02 | Chr9:134011298:C>T | Private mutation |
| NUP214 | Colorectal Cancer | p147_a05 | p.E225K | Private mutation |
| NUP214 | Colorectal Cancer | p147_a08 | p.E225K | Private mutation |
| NUP214 | Colorectal Cancer | p147_a09 | p.E225K | Private mutation |
| NUP214 | Colorectal Cancer | p155_p495 | p.V1574V | Private mutation |
| NUP214 | Esophageal Squamous Cell Carcinoma | p008_ESCC12 | p.S1484F | Trunk mutation |
| NUP214 | Esophageal Squamous Cell Carcinoma | p008_ESCC13 | p.S1618Y | Trunk mutation |
| NUP214 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.G149A | Branch mutation |
| NUP214 | Esophageal Squamous Cell Carcinoma | p128_P11 | Chr9:134073189:G>A | Private mutation |
| NUP214 | Esophageal Squamous Cell Carcinoma | p139_EC0990 | p.T370S | Private mutation |
| NUP214 | Gastric Adenocarcinoma | p011_MSI-H2 | p.S492C | Trunk mutation |
| NUP214 | Gastric Adenocarcinoma | p011_MSI-H2 | p.T628T | Trunk mutation |
| NUP214 | Gastric Carcinoma | p106_GC07 | p.L834V | Private mutation |
| NUP214 | Glioblastoma | p113_case03 | p.S518Nfs*9 | Private mutation |
| NUP214 | Glioblastoma | p113_case26 | p.A1489S | Private mutation |
| NUP214 | Glioma | p168_P01 | p.E855K | Branch mutation |
| NUP214 | Glioma | p168_P01 | p.P1791L | Branch mutation |
| NUP214 | Glioma | p168_P01 | p.G1727E | Private mutation |
| NUP214 | Glioma | p168_P18 | p.G2087S | Private mutation |
| NUP214 | Hepatocellular Carcinoma | p151_HCC5647 | Chr9:134073651:G>A | Trunk mutation |
| NUP214 | Lung Cancer | p021_L001 | p.A937G | Trunk mutation |
| NUP214 | Non-Small Cell Lung Cancer | p107_P022 | p.Q1209K | Branch mutation |
| NUP214 | Medulloblastoma | p072_MB7 | Chr9:134010423:C>T | Private mutation |
| NUP214 | Clear Cell Renal Cell Carcinoma | p019_RK26 | Chr9:134073605:p.P>L | Branch mutation |
| NUP214 | Renal Cell Carcinoma | p073_RCC7 | Chr9:134073605:C>T | Branch mutation |
| NUP214 | Urothelial Carcinoma | p031_WCM088 | p.P1386P | Private mutation |