Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
ATG2A |
Breast Cancer | p143_p1 |
Chr11:64664918:C>G |
Private mutation |
ATG2A |
Colorectal Cancer | p004_CRC_A01 |
Chr11:64677309:C>T |
Private mutation |
ATG2A |
Colorectal Cancer | p014_CRC1 |
c.3615_3615delinsGC |
Private mutation |
ATG2A |
Colorectal Cancer | p040_case9 |
Chr11:64673804:A>G |
Private mutation |
ATG2A |
Colorectal Cancer | p147_a03 |
p.D333G |
Private mutation |
ATG2A |
Colorectal Cancer | p147_a18 |
p.V1689A |
Private mutation |
ATG2A |
Colorectal Cancer | p147_a20 |
p.R1916H |
Trunk mutation |
ATG2A |
Colorectal Cancer | p155_p385 |
p.Q1299Q |
Private mutation |
ATG2A |
Colorectal Cancer | p155_p496 |
p.X788_splice |
Private mutation |
ATG2A |
Esophageal Squamous Cell Carcinoma | p008_ESCC09 |
p.G978E |
Trunk mutation |
ATG2A |
Esophageal Squamous Cell Carcinoma | p008_ESCC13 |
p.P712L |
Trunk mutation |
ATG2A |
Esophageal Squamous Cell Carcinoma | p124_ESCC005 |
p.P846T |
Private mutation |
ATG2A |
Esophageal Squamous Cell Carcinoma | p128_P19 |
Chr11:64680540:G>A |
Private mutation |
ATG2A |
Esophageal Squamous Cell Carcinoma | p139_EC1110 |
p.Q1867X |
Private mutation |
ATG2A |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.G1040G |
Trunk mutation |
ATG2A |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.D215D |
Branch mutation |
ATG2A |
Glioblastoma | p113_case02 |
p.V216M |
Branch mutation |
ATG2A |
Glioblastoma | p113_case07 |
p.A1873T |
Private mutation |
ATG2A |
Glioma | p168_P01 |
p.E1343E |
Private mutation |
ATG2A |
Hepatocellular Carcinoma | p151_HCC8257 |
Chr11:64673107:C>T |
Branch mutation |
ATG2A |
Non-Small Cell Lung Cancer | p107_P016 |
p.A1367S |
Private mutation |
ATG2A |
Ovarian Cancer | p144_AOCS091 |
p.D1357E |
Private mutation |
ATG2A |
Ovarian Cancer | p144_AOCS094 |
p.A879D |
Private mutation |
ATG2A |
Ovarian Cancer | p153_RJOC08 |
p.R717C |
Private mutation |
ATG2A |
Prostate Cancer | p164_P2 |
p.P656R |
Branch mutation |
ATG2A |
Prostate Cancer | p164_P2 |
p.T632M |
Private mutation |
ATG2A |
Urothelial Carcinoma | p031_WCM088 |
p.T632T |
Private mutation |