| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| PLXNB2 | Breast Cancer | p143_p5 | Chr22:50717121:C>G | Trunk mutation |
| PLXNB2 | Breast Cancer | p143_p5 | Chr22:50728906:G>A | Private mutation |
| PLXNB2 | Colorectal Cancer | p001_PCRC16 | Chr22:50727511:C>T | Trunk mutation |
| PLXNB2 | Colorectal Cancer | p004_CRC_A01 | Chr22:50727973:G>A | Private mutation |
| PLXNB2 | Colorectal Cancer | p034_MSU2 | Chr22:50728647:G>A | Trunk mutation |
| PLXNB2 | Colorectal Cancer | p104_UC03 | p.W1689C | Private mutation |
| PLXNB2 | Colorectal Cancer | p104_UC07 | p.F1100L | Branch mutation |
| PLXNB2 | Colorectal Cancer | p155_p251 | p.F723L | Private mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.V949V | Branch mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.I1019I | Branch mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.L1119V | Branch mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p124_ESCC026 | p.R23fs | Trunk mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p124_ESCC029 | p.V1467V | Branch mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p124_ESCC031 | p.G139R | Trunk mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p124_ESCC036 | p.E1398Q | Private mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p128_P11 | Chr22:50714204:C>T | Private mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p128_P21 | Chr22:50727947:C>T | Private mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p128_P24 | Chr22:50720419:C>A | Branch mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p128_SP28 | Chr22:50728774:G>A | Private mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p139_EC1125 | p.V51M | Branch mutation |
| PLXNB2 | Esophageal Squamous Cell Carcinoma | p139_EC1134 | p.S1009N | Private mutation |
| PLXNB2 | Gastric Adenocarcinoma | p011_MSI-H2 | p.N759D | Trunk mutation |
| PLXNB2 | Gastric Adenocarcinoma | p011_MSI-H2 | p.Q1036Q | Trunk mutation |
| PLXNB2 | Gastric Carcinoma | p106_GC04 | p.E1619K | Private mutation |
| PLXNB2 | Gastric Carcinoma | p106_GC07 | p.L11P | Private mutation |
| PLXNB2 | Gastric Carcinoma | p106_GC09 | p.Y1755C | Private mutation |
| PLXNB2 | Gastric Carcinoma | p106_GC13 | p.R241W | Private mutation |
| PLXNB2 | Glioblastoma | p113_case07 | p.G829D | Private mutation |
| PLXNB2 | Glioblastoma | p113_case14 | p.T679P | Private mutation |
| PLXNB2 | Glioblastoma | p113_case16 | p.N802D | Trunk mutation |
| PLXNB2 | Glioblastoma | p113_case21 | p.N802D | Trunk mutation |
| PLXNB2 | Glioblastoma | p113_case37 | p.N802D | Trunk mutation |
| PLXNB2 | Intrahepatic Cholangiocarcinoma | p080_ICC772 | p.R857Q | Private mutation |
| PLXNB2 | Hepatocellular Carcinoma | p029_case | - | Branch mutation |
| PLXNB2 | Hepatocellular Carcinoma | p151_HCC5647 | Chr22:50717305:T>A | Trunk mutation |
| PLXNB2 | Melanoma | p043_H | p.P105S | Private mutation |
| PLXNB2 | Melanoma | p043_H | p.A534V | Private mutation |
| PLXNB2 | Prostate Cancer | p116_PS352 | c.1098_1098delinsCG | Private mutation |
| PLXNB2 | Prostate Cancer | p117_PrCa14 | - | Private mutation |
| PLXNB2 | Prostate Cancer | p164_P2 | p.H1370R | Private mutation |
| PLXNB2 | Prostate Cancer | p164_P2 | p.K318E | Private mutation |
| PLXNB2 | Syndromic Neuroendocrine Carcinoma | p127_C4 | p.I82V | Private mutation |
| PLXNB2 | Renal Cell Carcinoma | p073_RCC3 | Chr22:50724369:G>A | Private mutation |
| PLXNB2 | Urothelial Carcinoma | p142_p10 | - | Trunk mutation |
| PLXNB2 | Urothelial Carcinoma | p142_p21 | - | Private mutation |