Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
TXLNB |
Breast Cancer | p143_p1 |
Chr6:139583799:G>C |
Private mutation |
TXLNB |
Colorectal Cancer | p004_CRC_A02 |
Chr6:139565671:C>T |
Private mutation |
TXLNB |
Colorectal Cancer | p034_MSU2 |
Chr6:139564345-139564346:AT>A |
Private mutation |
TXLNB |
Colorectal Cancer | p040_case9 |
Chr6:139564126:T>C |
Trunk mutation |
TXLNB |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.P655fs |
Private mutation |
TXLNB |
Esophageal Squamous Cell Carcinoma | p128_SP07 |
Chr6:139609730:G>A |
Private mutation |
TXLNB |
Esophageal Squamous Cell Carcinoma | p139_EC0966 |
p.Q307K |
Trunk mutation |
TXLNB |
Esophageal Squamous Cell Carcinoma | p139_EC1029 |
p.E351K |
Branch mutation |
TXLNB |
Esophageal Squamous Cell Carcinoma | p139_EC1117 |
p.Q624H |
Private mutation |
TXLNB |
Glioblastoma | p113_case08 |
p.G117* |
Private mutation |
TXLNB |
Hepatocellular Carcinoma | p061_P06 |
Chr6:139563857:C>T |
Trunk mutation |
TXLNB |
Lung Cancer | p154_p6 |
p.L278P |
Private mutation |
TXLNB |
Melanoma | p043_F |
p.S23L |
Trunk mutation |
TXLNB |
Renal Cancer | p018_patient2 |
Chr6:139581546:Del:TC |
Private mutation |
TXLNB |
Clear Cell Renal Cell Carcinoma | p019_EV002 |
Chr6:139581545:FS |
Private mutation |