| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| NUP210L | Breast Cancer | p123_case9 | p.V1553M | Trunk mutation |
| NUP210L | Osteosarcoma | p102_OS05 | Chr1:154112313:C>T | Private mutation |
| NUP210L | Colorectal Cancer | p034_MSU3 | Chr1:154067525-154067526:CA>C | Private mutation |
| NUP210L | Colorectal Cancer | p040_case9 | Chr1:154029311:A>G | Private mutation |
| NUP210L | Colorectal Cancer | p104_UC02 | p.V1322M | Branch mutation |
| NUP210L | Esophageal Squamous Cell Carcinoma | p124_ESCC002 | p.L780V | Trunk mutation |
| NUP210L | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | - | Private mutation |
| NUP210L | Esophageal Squamous Cell Carcinoma | p124_ESCC027 | p.E1799K | Private mutation |
| NUP210L | Esophageal Squamous Cell Carcinoma | p124_ESCC029 | p.P681S | Private mutation |
| NUP210L | Esophageal Squamous Cell Carcinoma | p124_ESCC045 | p.A695V | Branch mutation |
| NUP210L | Gastric Carcinoma | p106_GC09 | p.A6V | Private mutation |
| NUP210L | Gastric Carcinoma | p106_GC09 | p.E1679D | Private mutation |
| NUP210L | Anaplastic Astrocytoma | p070_HGG1 | Chr1:154108167:A>G | Branch mutation |
| NUP210L | Glioblastoma | p113_case02 | p.I1510_W1511del | Branch mutation |
| NUP210L | Glioblastoma | p113_case38 | p.T1486A | Private mutation |
| NUP210L | Glioma | p168_P18 | p.C1648C | Private mutation |
| NUP210L | Intrahepatic Cholangiocarcinoma | p080_ICC880 | p.V1123M | Trunk mutation |
| NUP210L | Intrahepatic Cholangiocarcinoma | p080_ICC1969 | p.A976S | Private mutation |
| NUP210L | Hepatocellular Carcinoma | p061_P05 | Chr1:154027291:T>C | Trunk mutation |
| NUP210L | Lung Adenocarcinoma | p017_317ss | Chr1:154112334:C>A | Trunk mutation |
| NUP210L | Medulloblastoma | p072_MB6 | Chr1:154108167:A>G | Trunk mutation |
| NUP210L | Melanoma | p043_D | p.P288S | Trunk mutation |
| NUP210L | Melanoma | p043_E | p.L58M | Private mutation |
| NUP210L | Ovarian Cancer | p153_RJOC05 | p.A1611V | Private mutation |
| NUP210L | Prostate Cancer | p105_1009 | p.I1714V | Private mutation |