Epithelial-Mesenchymal Transition gene database (dbEMT) Home
dbEMT
dbEMT 2.0
General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

177

Name

AGER

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.811T>A; p.W271R; 6:32182579-32182579

 pancreascarcinoma; adenocarcinomaSubstitution - Missense

c.697G>T; p.V233L; 6:32182693-32182693

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - Missense

c.394G>A; p.E132K; 6:32183350-32183350

 skinmalignant_melanomaSubstitution - Missense

c.93delC; p.E32fs*5; 6:32183947-32183947

 central_nervous_system; brainglioma; astrocytoma_Grade_IVDeletion - Frameshift

c.452C>A; p.P151H; 6:32183170-32183170

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.452C>A; p.P151H; 6:32183170-32183170

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.452C>A; p.P151H; 6:32183170-32183170

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.452C>A; p.P151H; 6:32183170-32183170

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.452C>A; p.P151H; 6:32183170-32183170

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.279T>C; p.D93D; 6:32183631-32183631

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.267C>G; p.V89V; 6:32183643-32183643

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.241A>C; p.N81H; 6:32183669-32183669

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.604C>T; p.P202S; 6:32182928-32182928

 skinmalignant_melanomaSubstitution - Missense

c.1045G>A; p.G349R; 6:32181424-32181424

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1017A>G; p.G339G; 6:32181452-32181452

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.762C>T; p.T254T; 6:32182628-32182628

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.121delG; p.A41fs*13; 6:32183919-32183919

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.199_200insC; p.Q67fs*28; 6:32183710-32183711

 lungcarcinoma; adenocarcinomaInsertion - Frameshift

c.826G>A; p.V276M; 6:32182385-32182385

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.355C>A; p.Q119K; 6:32183555-32183555

 skinmalignant_melanomaSubstitution - Missense

c.54G>A; p.G18G; 6:32183986-32183986

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.536G>C; p.R179T; 6:32182996-32182996

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.569C>T; p.S190L; 6:32182963-32182963

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1172C>T; p.S391L; 6:32181186-32181186

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.638G>T; p.G213V; 6:32182894-32182894

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.572A>G; p.E191G; 6:32182960-32182960

 livercarcinomaSubstitution - Missense

c.572A>G; p.E191G; 6:32182960-32182960

 livercarcinomaSubstitution - Missense

c.108G>A; p.L36L; 6:32183932-32183932

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.230G>C; p.R77P; 6:32183680-32183680

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.1200T>C; p.S400S; 6:32181158-32181158

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.540C>T; p.H180H; 6:32182992-32182992

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.243C>T; p.N81N; 6:32183667-32183667

 bone; pelvisEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.248C>A; p.S83Y; 6:32183662-32183662

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.341G>A; p.R114Q; 6:32183569-32183569

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.477G>A; p.L159L; 6:32183145-32183145

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.386C>T; p.S129F; 6:32183358-32183358

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.902G>C; p.C301S; 6:32182309-32182309

 pancreascarcinoma; adenocarcinomaSubstitution - Missense

c.1072A>G; p.I358V; 6:32181397-32181397

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.93C>G; p.G31G; 6:32183947-32183947

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.373G>A; p.E125K; 6:32183371-32183371

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.923A>C; p.H308P; 6:32182288-32182288

 bone; tibiaEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.691+5G>A; p.?; 6:32182836-32182836

 oesophaguscarcinoma; adenocarcinomaUnknown

c.1151A>G; p.E384G; 6:32181207-32181207

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.924C>T; p.H308H; 6:32182287-32182287

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.1162C>A; p.L388M; 6:32181196-32181196

 breastcarcinoma; ductal_carcinomaSubstitution - Missense

c.601G>A; p.D201N; 6:32182931-32182931

 skinmalignant_melanomaSubstitution - Missense

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