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

Basic Information

Gene ID

51129

Name

ANGPTL4

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.407G>A; p.R136Q; 19:8366042-8366042

 skin; extremitymalignant_melanomaSubstitution - Missense

c.407G>A; p.R136Q; 19:8366042-8366042

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.407G>A; p.R136Q; 19:8366042-8366042

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.868T>C; p.S290P; 19:8371351-8371351

 skinmalignant_melanomaSubstitution - Missense

c.429G>C; p.Q143H; 19:8366064-8366064

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.429G>C; p.Q143H; 19:8366064-8366064

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.429G>C; p.Q143H; 19:8366064-8366064

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.429G>C; p.Q143H; 19:8366064-8366064

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.429G>C; p.Q143H; 19:8366064-8366064

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.429G>A; p.Q143Q; 19:8366064-8366064

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.429G>A; p.Q143Q; 19:8366064-8366064

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.675A>C; p.T225T; 19:8371069-8371069

 autonomic_ganglianeuroblastomaSubstitution - coding silent

c.1012G>T; p.D338Y; 19:8371495-8371495

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.21_22insG; p.A9fs*86; 19:8364342-8364343

 oesophaguscarcinoma; adenocarcinomaInsertion - Frameshift

c.870C>T; p.S290S; 19:8371353-8371353

 skinmalignant_melanomaSubstitution - coding silent

c.730T>C; p.Y244H; 19:8371124-8371124

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.442G>A; p.D148N; 19:8366214-8366214

 skinmalignant_melanomaSubstitution - Missense

c.1070C>G; p.S357C; 19:8373735-8373735

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.544C>T; p.H182Y; 19:8366316-8366316

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.509A>T; p.Q170L; 19:8366281-8366281

 skinmalignant_melanomaSubstitution - Missense

c.1024G>A; p.A342T; 19:8371507-8371507

 boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.517G>C; p.D173H; 19:8366289-8366289

 pancreascarcinomaSubstitution - Missense

c.1102C>T; p.P368S; 19:8373767-8373767

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.334C>A; p.Q112K; 19:8365969-8365969

 adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningSubstitution - Missense

c.1134C>G; p.I378M; 19:8373799-8373799

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.245G>T; p.G82V; 19:8364566-8364566

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.791G>A; p.S264N; 19:8371274-8371274

 skin; facecarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.106G>T; p.A36S; 19:8364427-8364427

 livercarcinomaSubstitution - Missense

c.198G>C; p.L66L; 19:8364519-8364519

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.958A>T; p.S320C; 19:8371441-8371441

 livercarcinomaSubstitution - Missense

c.529A>C; p.N177H; 19:8366301-8366301

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.801G>A; p.G267G; 19:8371284-8371284

 skinmalignant_melanomaSubstitution - coding silent

c.797C>T; p.T266M; 19:8371280-8371280

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1167G>A; p.P389P; 19:8373832-8373832

 breastcarcinomaSubstitution - coding silent

c.629C>T; p.P210L; 19:8369300-8369300

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.960C>T; p.S320S; 19:8371443-8371443

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.607G>A; p.E203K; 19:8369278-8369278

 skinmalignant_melanomaSubstitution - Missense

c.621G>C; p.Q207H; 19:8369292-8369292

 skinmalignant_melanomaSubstitution - Missense

c.1113G>A; p.R371R; 19:8373778-8373778

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.1007G>A; p.R336H; 19:8371490-8371490

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.393G>A; p.E131E; 19:8366028-8366028

 skinmalignant_melanomaSubstitution - coding silent

c.538_539insGCCT; p.H182fs*23; 19:8366310-8366311

 skinmalignant_melanomaInsertion - Frameshift

c.1112G>A; p.R371Q; 19:8373777-8373777

 oesophaguscarcinomaSubstitution - Missense

c.382C>T; p.R128W; 19:8366017-8366017

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1066C>G; p.H356D; 19:8373731-8373731

 skinmalignant_melanomaSubstitution - Missense

c.756C>T; p.H252H; 19:8371150-8371150

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; mast_cell_neoplasmSubstitution - coding silent

c.327C>G; p.L109L; 19:8365962-8365962

 breastcarcinomaSubstitution - coding silent

c.756C>T; p.H252H; 19:8371150-8371150

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasmSubstitution - coding silent

c.762G>C; p.E254D; 19:8371245-8371245

 breastcarcinomaSubstitution - Missense

c.469G>A; p.A157T; 19:8366241-8366241

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.872T>A; p.V291E; 19:8371355-8371355

 thyroidcarcinomaSubstitution - Missense

c.519C>A; p.D173E; 19:8366291-8366291

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.912C>T; p.L304L; 19:8371395-8371395

 skinmalignant_melanomaSubstitution - coding silent

c.957C>G; p.P319P; 19:8371440-8371440

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.188G>A; p.R63H; 19:8364509-8364509

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.547+1G>A; p.?; 19:8366320-8366320

 large_intestine; rectumadenomaUnknown

c.939C>T; p.G313G; 19:8371422-8371422

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.521C>T; p.P174L; 19:8366293-8366293

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.517G>A; p.D173N; 19:8366289-8366289

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.538C>T; p.R180C; 19:8366310-8366310

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

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