Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
FMN2 |
Breast Cancer | p111_p3-92 |
p.P1032L |
Branch mutation |
FMN2 |
Breast Cancer | p123_case2 |
p.G1281G |
Trunk mutation |
FMN2 |
Breast Cancer | p123_case2 |
p.H1384H |
Private mutation |
FMN2 |
Breast Cancer | p123_case3 |
p.S1533N |
Trunk mutation |
FMN2 |
Breast Cancer | p123_case9 |
p.Q1554Q |
Trunk mutation |
FMN2 |
Osteosarcoma | p102_OS01 |
Chr1:240255906:C>T |
Branch mutation |
FMN2 |
Colorectal Cancer | p014_CRC1 |
p.L1412L |
Trunk mutation |
FMN2 |
Colorectal Cancer | p014_CRC3 |
p.D720N |
Trunk mutation |
FMN2 |
Colorectal Cancer | p014_CRC5 |
p.A962A |
Private mutation |
FMN2 |
Colorectal Cancer | p034_MSS1 |
Chr1:240492396:C>T |
Private mutation |
FMN2 |
Colorectal Cancer | p034_MSU1 |
Chr1:240256798:C>T |
Trunk mutation |
FMN2 |
Colorectal Cancer | p034_MSU1 |
Chr1:240370926:C>T |
Private mutation |
FMN2 |
Colorectal Cancer | p034_MSU1 |
Chr1:240370992:C>T |
Private mutation |
FMN2 |
Colorectal Cancer | p034_MSU4 |
Chr1:240493907:T>TA |
Private mutation |
FMN2 |
Colorectal Cancer | p155_p492 |
p.L1703L |
Private mutation |
FMN2 |
Colorectal Cancer | p155_p494 |
p.I794M |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p008_ESCC06 |
p.K1717K |
Branch mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC007 |
p.S124L |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC010 |
p.Q242K |
Trunk mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC011 |
p.G939V |
Trunk mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.G512G |
Trunk mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC023 |
p.A463V |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC029 |
p.P936S |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC034 |
p.L798L |
Trunk mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p128_P01 |
Chr1:240370489:C>T |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p128_P19 |
Chr1:240370637:A>G |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p139_EC0966 |
p.H1635P |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p139_EC1020 |
p.P628S |
Private mutation |
FMN2 |
Esophageal Squamous Cell Carcinoma | p139_EC1117 |
p.L1651V |
Private mutation |
FMN2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.H1418H |
Trunk mutation |
FMN2 |
Gastric Carcinoma | p106_GC07 |
p.F1557Y |
Private mutation |
FMN2 |
Gastric Carcinoma | p106_GC09 |
p.G155R |
Private mutation |
FMN2 |
Gastric Carcinoma | p106_GC12 |
p.E191D |
Trunk mutation |
FMN2 |
Gastric Carcinoma | p106_GC13 |
p.P1266A |
Private mutation |
FMN2 |
Gastric Carcinoma | p106_GC13 |
p.934_945del |
Private mutation |
FMN2 |
Gastric Carcinoma | p106_GC15 |
p.G371G |
Trunk mutation |
FMN2 |
Glioblastoma | p070_HGG2 |
Chr1:240448602:C>A |
Branch mutation |
FMN2 |
Intrahepatic Cholangiocarcinoma | p080_ICC1370 |
p.G941A |
Branch mutation |
FMN2 |
Lung Adenocarcinoma | p017_317ss |
Chr1:240256729:C>A |
Trunk mutation |
FMN2 |
Lung Adenocarcinoma | p017_317ss |
Chr1:240497209:C>T |
Trunk mutation |
FMN2 |
Small Cell Lung Carcinoma | p100_p4 |
Chr1:240351521:G>T |
Trunk mutation |
FMN2 |
Small Cell Lung Carcinoma | p100_p5 |
Chr1:240256611:C>A |
Trunk mutation |
FMN2 |
Non-Small Cell Lung Cancer | p107_P007 |
p.D171N |
Trunk mutation |
FMN2 |
Non-Small Cell Lung Cancer | p138_p001 |
p.E1640K |
Branch mutation |
FMN2 |
Non-Small Cell Lung Cancer | p163_P001 |
p.E1640K |
Branch mutation |
FMN2 |
Melanoma | p043_A |
p.P1207L |
Trunk mutation |
FMN2 |
Melanoma | p043_A |
p.G1700E |
Trunk mutation |
FMN2 |
Melanoma | p043_B |
p.P1247S |
Trunk mutation |
FMN2 |
Melanoma | p043_C |
p.G1484S |
Trunk mutation |
FMN2 |
Melanoma | p043_F |
p.P410L |
Trunk mutation |
FMN2 |
Melanoma | p043_F |
p.P1098S |
Trunk mutation |
FMN2 |
Melanoma | p043_F |
p.P1136S |
Trunk mutation |
FMN2 |
Ovarian Serous Carcinomas | p006_OSC2 |
p.P999P |
Private mutation |
FMN2 |
Ovarian Cancer | p052_Case3 |
- |
Private mutation |
FMN2 |
Prostate Cancer | p116_PS155 |
p.P1055P |
Branch mutation |
FMN2 |
Renal Cell Carcinoma | p073_RCC5 |
Chr1:240306634:A>G |
Private mutation |
FMN2 |
Urothelial Carcinoma | p031_WCM077 |
p.D685Y |
Branch mutation |
FMN2 |
Urothelial Carcinoma | p142_p36 |
- |
Private mutation |