| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| XDH | Breast Cancer | p091_A1 | p.V1196 | Branch mutation |
| XDH | Breast Cancer | p143_p1 | Chr2:31620490:C>A | Private mutation |
| XDH | Breast Cancer | p143_p5 | Chr2:31595104:C>T | Branch mutation |
| XDH | Osteosarcoma | p112_OS1101 | p.E1211G | Branch mutation |
| XDH | Colorectal Cancer | p001_PCRC13 | Chr2:31573023:G>A | Private mutation |
| XDH | Colorectal Cancer | p004_CRC_A04 | Chr2:31595198:G>T | Private mutation |
| XDH | Colorectal Cancer | p034_MSU4 | Chr2:31609299:G>A | Trunk mutation |
| XDH | Colorectal Cancer | p040_case9 | Chr2:31591460:C>A | Trunk mutation |
| XDH | Colorectal Cancer | p040_case9 | Chr2:31621533:G>A | Branch mutation |
| XDH | Esophageal Squamous Cell Carcinoma | p008_ESCC03 | p.S1215C | Branch mutation |
| XDH | Esophageal Squamous Cell Carcinoma | p008_ESCC04 | p.V629D | Private mutation |
| XDH | Esophageal Squamous Cell Carcinoma | p128_P03 | Chr2:31590878:G>C | Private mutation |
| XDH | Esophageal Squamous Cell Carcinoma | p128_P08 | Chr2:31600070:C>T | Private mutation |
| XDH | Esophageal Squamous Cell Carcinoma | p128_SP03 | Chr2:31590878:G>C | Private mutation |
| XDH | Gastric Carcinoma | p106_GC09 | p.G528G | Private mutation |
| XDH | Glioma | p168_P01 | p.G739S | Private mutation |
| XDH | Lung Adenocarcinoma | p017_317ss | Chr2:31571741:G>A | Trunk mutation |
| XDH | Lung Adenocarcinoma | p134_A006 | p.D584N | Branch mutation |
| XDH | Melanoma | p043_F | p.E970K | Trunk mutation |
| XDH | Melanoma | p043_H | p.T469I | Private mutation |
| XDH | Melanoma | p135_p11 | Chr2:31625933:G>A | Trunk mutation |
| XDH | Melanoma | p135_p12 | Chr2:31589798:G>A | Trunk mutation |
| XDH | Melanoma | p135_p27 | Chr2:31595158:G>A | Trunk mutation |
| XDH | Ovarian Cancer | p052_Case2 | p.I737F | Trunk mutation |
| XDH | Ovarian Cancer | p144_AOCS139 | - | Private mutation |
| XDH | Renal Cancer | p085_rcc-vtt-4 | - | Branch mutation |
| XDH | Renal Cell Carcinoma | p073_RCC3 | Chr2:31571116:C>T | Private mutation |