Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
SLIT2 |
Colorectal Cancer | p034_MSU3 |
Chr4:20550718:G>A |
Trunk mutation |
SLIT2 |
Colorectal Cancer | p155_p492 |
p.C1064dup |
Private mutation |
SLIT2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC016 |
p.R726H |
Trunk mutation |
SLIT2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC027 |
p.R1454P |
Branch mutation |
SLIT2 |
Esophageal Squamous Cell Carcinoma | p128_P19 |
Chr4:20535226:G>C |
Private mutation |
SLIT2 |
Esophageal Squamous Cell Carcinoma | p128_SP23 |
Chr4:20598171:C>T |
Private mutation |
SLIT2 |
Esophageal Squamous Cell Carcinoma | p128_SP23 |
Chr4:20541071:A>G |
Private mutation |
SLIT2 |
Esophageal Squamous Cell Carcinoma | p128_SP24 |
Chr4:20555454:G>A |
Trunk mutation |
SLIT2 |
Gastric Adenocarcinoma | p011_MSI-H1 |
p.G1258D |
Private mutation |
SLIT2 |
Gastric Carcinoma | p106_GC01 |
p.T57T |
Private mutation |
SLIT2 |
Gastric Carcinoma | p106_GC14 |
p.G1324R |
Private mutation |
SLIT2 |
Gastric Carcinoma | p106_GC15 |
p.T606T |
Private mutation |
SLIT2 |
Glioblastoma | p113_case01 |
p.A421T |
Private mutation |
SLIT2 |
Glioblastoma | p113_case07 |
p.A45T |
Private mutation |
SLIT2 |
Glioblastoma | p113_case07 |
p.S1511F |
Private mutation |
SLIT2 |
Glioblastoma | p113_case08 |
p.I816L |
Private mutation |
SLIT2 |
Glioblastoma | p113_case36 |
p.S831Y |
Private mutation |
SLIT2 |
Intrahepatic Cholangiocarcinoma | p080_ICC1239 |
p.L419F |
Private mutation |
SLIT2 |
Hepatocellular Carcinoma | p151_HCC6046 |
Chr4:20555443:C>T |
Trunk mutation |
SLIT2 |
Lung Adenocarcinoma | p017_4990 |
Chr4:20555910:G>A |
Branch mutation |
SLIT2 |
Melanoma | p043_A |
p.R1212W |
Trunk mutation |
SLIT2 |
Melanoma | p043_H |
p.D394N |
Private mutation |
SLIT2 |
Ovarian Cancer | p144_AOCS088 |
p.R348C |
Trunk mutation |
SLIT2 |
Ovarian Cancer | p144_AOCS139 |
p.D727E |
Branch mutation |
SLIT2 |
Ovarian Cancer | p153_RJOC08 |
p.C1143Y |
Private mutation |
SLIT2 |
Renal Cell Carcinoma | p073_RCC6 |
Chr4:20482331:T>C |
Branch mutation |
SLIT2 |
Renal Cell Carcinoma | p073_RCC9 |
Chr4:20525485:C>T |
Private mutation |