Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
FAM47C |
Colorectal Cancer | p001_PCRC05 |
ChrX:37029016:C>T |
Private mutation |
FAM47C |
Colorectal Cancer | p034_MSS3 |
ChrX:37027802:C>T |
Private mutation |
FAM47C |
Colorectal Cancer | p155_p494 |
p.R739H |
Trunk mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p008_ESCC04 |
p.V627L |
Trunk mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p008_ESCC05 |
p.F30F |
Trunk mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p124_ESCC001 |
p.P608Q |
Trunk mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p128_P02 |
ChrX:37026576:G>A |
Branch mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p128_SP13 |
ChrX:37026659:G>A |
Trunk mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p128_SP19 |
ChrX:37026614:A>C |
Private mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p128_SP23 |
ChrX:37028041:T>C |
Private mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p139_EC1125 |
p.T457I |
Branch mutation |
FAM47C |
Esophageal Squamous Cell Carcinoma | p139_EC1125 |
p.R458L |
Branch mutation |
FAM47C |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.P548P |
Trunk mutation |
FAM47C |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.N924T |
Trunk mutation |
FAM47C |
Gastric Carcinoma | p106_GC09 |
p.R523C |
Private mutation |
FAM47C |
Gastric Carcinoma | p106_GC11 |
p.V483I |
Trunk mutation |
FAM47C |
Glioma | p168_P01 |
p.E237K |
Private mutation |
FAM47C |
Glioma | p168_P18 |
p.P814P |
Private mutation |
FAM47C |
Intrahepatic Cholangiocarcinoma | p080_ICC1969 |
p.R458W |
Branch mutation |
FAM47C |
Hepatocellular Carcinoma | p151_HCC5647 |
ChrX:37028724:T>A |
Branch mutation |
FAM47C |
Lung Adenocarcinoma | p017_499s |
ChrX:37028903:G>T |
Branch mutation |
FAM47C |
Lung Adenocarcinoma | p083_X499 |
- |
Branch mutation |
FAM47C |
Small Cell Lung Carcinoma | p100_p5 |
ChrX:37026579:G>T |
Trunk mutation |
FAM47C |
Melanoma | p043_A |
p.E120K |
Trunk mutation |
FAM47C |
Ovarian Serous Carcinomas | p006_OSC2 |
p.T565A |
Private mutation |
FAM47C |
Prostate Cancer | p105_1020 |
p.L606I |
Branch mutation |
FAM47C |
Clear Cell Renal Cell Carcinoma | p019_EV007 |
ChrX:37029565:p.V>I |
Private mutation |
FAM47C |
Renal Cell Carcinoma | p073_RCC4 |
ChrX:37026638:C>G |
Trunk mutation |
FAM47C |
Renal Cell Carcinoma | p073_RCC6 |
ChrX:37029565:G>A |
Branch mutation |
FAM47C |
Urothelial Carcinoma | p031_WCM077 |
p.V118I |
Private mutation |
FAM47C |
Urothelial Carcinoma | p031_WCM077 |
p.R523H |
Private mutation |
FAM47C |
Urothelial Carcinoma | p031_WCM117 |
p.R523H |
Branch mutation |
FAM47C |
Urothelial Carcinoma | p031_WCM168 |
p.R523H |
Private mutation |