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

Basic Information

Gene ID

3553

Name

IL1B

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.657G>T; p.K219N; 2:112830514-112830514

 thyroidother; neoplasmSubstitution - Missense

c.588A>G; p.L196L; 2:112831301-112831301

 skinmalignant_melanomaSubstitution - coding silent

c.580C>A; p.P194T; 2:112831309-112831309

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.300_301insA; p.E101fs*10; 2:112833374-112833375

 skin; neckmalignant_melanomaInsertion - Frameshift

c.645_671del27; p.V216_N224delVFNKIEINN; 2:112830500-112830526

 skin; head_neckcarcinoma; squamous_cell_carcinomaDeletion - In frame

c.608C>A; p.P203H; 2:112830563-112830563

 autonomic_ganglianeuroblastomaSubstitution - Missense

c.266A>G; p.D89G; 2:112833409-112833409

 skinmalignant_melanomaSubstitution - Missense

c.245C>T; p.P82L; 2:112833430-112833430

 livercarcinomaSubstitution - Missense

c.245C>T; p.P82L; 2:112833430-112833430

 livercarcinomaSubstitution - Missense

c.552C>A; p.Y184*; 2:112831337-112831337

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Nonsense

c.567G>A; p.L189L; 2:112831322-112831322

 skinmalignant_melanomaSubstitution - coding silent

c.612A>C; p.K204N; 2:112830559-112830559

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.331G>A; p.E111K; 2:112832797-112832797

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.331G>A; p.E111K; 2:112832797-112832797

 breastcarcinoma; ER-PR-positive_carcinomaSubstitution - Missense

c.331G>A; p.E111K; 2:112832797-112832797

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.699C>T; p.F233F; 2:112830472-112830472

 skinmalignant_melanomaSubstitution - coding silent

c.467-3C>T; p.?; 2:112831425-112831425

 lungcarcinoma; squamous_cell_carcinomaUnknown

c.315C>T; p.F105F; 2:112832813-112832813

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.7G>A; p.E3K; 2:112836223-112836223

 skinmalignant_melanomaSubstitution - Missense

c.786C>A; p.F262L; 2:112830385-112830385

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.195G>A; p.A65A; 2:112833480-112833480

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.543G>T; p.K181N; 2:112831346-112831346

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.669T>C; p.N223N; 2:112830502-112830502

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.747C>T; p.F249F; 2:112830424-112830424

 skinmalignant_melanomaSubstitution - coding silent

c.747C>T; p.F249F; 2:112830424-112830424

 skinmalignant_melanomaSubstitution - coding silent

c.93G>A; p.Q31Q; 2:112835572-112835572

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.694C>T; p.Q232*; 2:112830477-112830477

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.33G>A; p.M11I; 2:112836197-112836197

 skinmalignant_melanomaSubstitution - Missense

c.330C>T; p.N110N; 2:112832798-112832798

 pituitary; craniopharyngeal_ductcraniopharyngioma; adamantinomatousSubstitution - coding silent

c.105C>T; p.S35S; 2:112833570-112833570

 central_nervous_system; braingliomaSubstitution - coding silent

c.378C>G; p.L126L; 2:112832750-112832750

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.435C>T; p.L145L; 2:112832693-112832693

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.374C>T; p.T125M; 2:112832754-112832754

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.121C>A; p.L41I; 2:112833554-112833554

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.307A>T; p.I103F; 2:112832821-112832821

 pancreascarcinoma; ductal_carcinomaSubstitution - Missense

c.319A>T; p.T107S; 2:112832809-112832809

 breastcarcinoma; basal_(triple-negative)_carcinomaSubstitution - Missense

c.151C>T; p.R51*; 2:112833524-112833524

 stomachcarcinoma; adenocarcinomaSubstitution - Nonsense

c.139G>T; p.G47C; 2:112833536-112833536

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.559T>G; p.C187G; 2:112831330-112831330

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.494G>A; p.G165E; 2:112831395-112831395

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.259G>T; p.E87*; 2:112833416-112833416

 large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.99+1G>A; p.?; 2:112835565-112835565

 kidneyother; neoplasmUnknown

c.397_398insA; p.S133fs*9; 2:112832730-112832731

 large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.768C>A; p.G256G; 2:112830403-112830403

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.433C>T; p.L145F; 2:112832695-112832695

 skinmalignant_melanomaSubstitution - Missense

c.806C>T; p.S269F; 2:112830365-112830365

 skinmalignant_melanomaSubstitution - Missense

c.325G>A; p.D109N; 2:112832803-112832803

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.538G>A; p.E180K; 2:112831351-112831351

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.538G>A; p.E180K; 2:112831351-112831351

 skinmalignant_melanomaSubstitution - Missense

c.553C>T; p.L185L; 2:112831336-112831336

 pancreascarcinomaSubstitution - coding silent

c.33G>T; p.M11I; 2:112836197-112836197

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.640C>T; p.R214*; 2:112830531-112830531

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.640C>T; p.R214*; 2:112830531-112830531

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.640C>T; p.R214*; 2:112830531-112830531

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Nonsense

c.771G>T; p.Q257H; 2:112830400-112830400

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.416C>T; p.P139L; 2:112832712-112832712

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.114C>T; p.D38D; 2:112833561-112833561

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.152G>A; p.R51Q; 2:112833523-112833523

 skinmalignant_melanomaSubstitution - Missense

c.152G>A; p.R51Q; 2:112833523-112833523

 skinmalignant_melanomaSubstitution - Missense

c.152G>A; p.R51Q; 2:112833523-112833523

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.738G>A; p.M246I; 2:112830433-112830433

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.139G>A; p.G47S; 2:112833536-112833536

 pancreascarcinoma; ductal_carcinomaSubstitution - Missense

c.345C>T; p.H115H; 2:112832783-112832783

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.96G>A; p.M32I; 2:112835569-112835569

 skinmalignant_melanomaSubstitution - Missense

c.666C>A; p.I222I; 2:112830505-112830505

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.359G>A; p.R120Q; 2:112832769-112832769

 skinmalignant_melanomaSubstitution - Missense

c.202G>T; p.V68F; 2:112833473-112833473

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.365T>G; p.L122R; 2:112832763-112832763

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.624G>A; p.K208K; 2:112830547-112830547

 skinmalignant_melanomaSubstitution - coding silent

c.421G>A; p.E141K; 2:112832707-112832707

 skinmalignant_melanomaSubstitution - Missense

c.197C>A; p.S66*; 2:112833478-112833478

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.657G>C; p.K219N; 2:112830514-112830514

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.630G>A; p.K210K; 2:112830541-112830541

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.752G>A; p.G251E; 2:112830419-112830419

 skinmalignant_melanomaSubstitution - Missense

c.537G>A; p.K179K; 2:112831352-112831352

 skinmalignant_melanomaSubstitution - coding silent

c.661G>T; p.E221*; 2:112830510-112830510

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.661G>T; p.E221*; 2:112830510-112830510

 large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.562G>A; p.V188M; 2:112831327-112831327

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - Missense

c.214G>A; p.D72N; 2:112833461-112833461

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.22G>A; p.A8T; 2:112836208-112836208

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.468G>A; p.V156V; 2:112831421-112831421

 bone; tibiachondrosarcomaSubstitution - coding silent

c.28G>T; p.E10*; 2:112836202-112836202

 stomachcarcinoma; adenocarcinomaSubstitution - Nonsense

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