| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| GPHN | Osteosarcoma | p112_OS1107 | p.G36W | Private mutation |
| GPHN | Esophageal Squamous Cell Carcinoma | p128_P12 | Chr14:67579866:C>A | Private mutation |
| GPHN | Gastric Adenocarcinoma | p011_MSI-H2 | p.R686Q | Branch mutation |
| GPHN | Gastric Carcinoma | p106_GC07 | p.R491R | Private mutation |
| GPHN | Glioblastoma | p070_HGG2 | Chr14:67646168:C>A | Private mutation |
| GPHN | Glioblastoma | p070_HGG3 | Chr14:67452451:T>C | Private mutation |
| GPHN | Intrahepatic Cholangiocarcinoma | p080_ICC892 | p.I235V | Branch mutation |
| GPHN | Melanoma | p010_Mm1765 | - | Trunk mutation |
| GPHN | Prostate Cancer | p118_CPCG0103 | p.E105Q | Branch mutation |
| GPHN | Clear Cell Renal Cell Carcinoma | p019_RMH004 | Chr14:67555711:Stop codon | Branch mutation |
| GPHN | Renal Cell Carcinoma | p073_RCC4 | Chr14:67228815:T>C | Private mutation |
| GPHN | Renal Cell Carcinoma | p073_RCC9 | Chr14:67555711:C>T | Branch mutation |