Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
GRM6 |
Osteosarcoma | p112_OS1101 |
E10_UTR_3 |
Private mutation |
GRM6 |
Colorectal Cancer | p034_MSU2 |
Chr5:178408717:T>C |
Trunk mutation |
GRM6 |
Colorectal Cancer | p155_p335 |
p.G338R |
Private mutation |
GRM6 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.S198C |
Private mutation |
GRM6 |
Esophageal Squamous Cell Carcinoma | p124_ESCC018 |
p.V234D |
Private mutation |
GRM6 |
Esophageal Squamous Cell Carcinoma | p124_ESCC034 |
p.L832L |
Private mutation |
GRM6 |
Esophageal Squamous Cell Carcinoma | p139_EC0959 |
p.A667S |
Trunk mutation |
GRM6 |
Gastric Adenocarcinoma | p011_MSS2 |
p.V148I |
Private mutation |
GRM6 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.E70K |
Branch mutation |
GRM6 |
Anaplastic Astrocytoma | p070_HGG1 |
Chr5:178412702:T>A |
Trunk mutation |
GRM6 |
Glioblastoma | p113_case01 |
p.V490M |
Private mutation |
GRM6 |
Hepatocellular Carcinoma | p157_p3 |
p.E70V |
Trunk mutation |
GRM6 |
Lung Adenocarcinoma | p017_330 |
Chr5:178408767:A>T |
Trunk mutation |
GRM6 |
Lung Adenocarcinoma | p017_472 |
Chr5:178417579:G>T |
Trunk mutation |
GRM6 |
Lung Adenocarcinoma | p017_499s |
Chr5:178419180:G>T |
Trunk mutation |
GRM6 |
Lung Adenocarcinoma | p083_X330 |
- |
Trunk mutation |
GRM6 |
Melanoma | p043_A |
p.P690L |
Trunk mutation |
GRM6 |
Melanoma | p043_F |
p.R346Q |
Trunk mutation |
GRM6 |
Melanoma | p043_G |
p.S685L |
Trunk mutation |
GRM6 |
Melanoma | p135_p11 |
Chr5:178418481:G>A |
Trunk mutation |
GRM6 |
Melanoma | p135_p12 |
Chr5:178418903:C>T |
Private mutation |
GRM6 |
Melanoma | p135_p15 |
Chr5:178408667:G>A |
Private mutation |
GRM6 |
Melanoma | p135_p26 |
Chr5:178413186:G>A |
Trunk mutation |
GRM6 |
Ovarian Serous Carcinomas | p006_OSC1 |
p.L698L |
Branch mutation |
GRM6 |
Pancreatic Cancer | p054_Pa07 |
- |
Branch mutation |
GRM6 |
Renal Cell Carcinoma | p073_RCC3 |
Chr5:178418301:G>T |
Trunk mutation |
GRM6 |
Urothelial Carcinoma | p031_WCM088 |
p.V724M |
Private mutation |
GRM6 |
Urothelial Carcinoma | p031_WCM259 |
p.E222K |
Private mutation |