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Gene information | Literature | Expression | lncRNA | Mutation | Homolog

Basic Information

Gene ID

1871

Name

E2F3

Synonymous

E2F transcription factor 3;E2F3;E2F transcription factor 3

Definition

transcription factor E2F3

Position

6p22

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.823G>A; p.E275K; 6:20482859-20482859

breastcarcinomaSubstitution - Missense

c.1178C>A; p.S393Y; 6:20490210-20490210

breastcarcinomaSubstitution - Missense

c.1085_1088delAAAC; p.N364fs*54; 6:20488198-20488201

breastcarcinomaDeletion - Frameshift

c.742G>C; p.E248Q; 6:20482778-20482778

breastcarcinomaSubstitution - Missense

c.450A>T; p.L150F; 6:20479902-20479902

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.162G>C; p.P54P; 6:20402394-20402394

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.21C>T; p.P7P; 6:20402253-20402253

central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - coding silent

c.485G>A; p.R162Q; 6:20479937-20479937

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1344C>T; p.F448F; 6:20490376-20490376

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.139_150del12; p.A50_A53delAAAA; 6:20402371-20402382

endometriumcarcinoma; endometrioid_carcinomaDeletion - In frame

c.1167T>G; p.D389E; 6:20490199-20490199

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.867G>A; p.E289E; 6:20482903-20482903

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.658G>A; p.D220N; 6:20481358-20481358

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.272C>T; p.A91V; 6:20402504-20402504

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphomaSubstitution - Missense

c.1188C>G; p.N396K; 6:20490220-20490220

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.1138T>A; p.L380M; 6:20490170-20490170

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.666C>A; p.T222T; 6:20481366-20481366

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.77C>T; p.A26V; 6:20402309-20402309

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.85G>A; p.A29T; 6:20402317-20402317

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.523_524insA; p.T177fs*4; 6:20481223-20481224

large_intestine; caecumcarcinoma; adenocarcinomaInsertion - Frameshift

c.552T>C; p.G184G; 6:20481252-20481252

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1344C>T; p.F448F; 6:20490376-20490376

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.915delA; p.I307fs*10; 6:20486719-20486719

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.662T>C; p.I221T; 6:20481362-20481362

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1249A>G; p.N417D; 6:20490281-20490281

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.5G>T; p.R2I; 6:20402237-20402237

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.741T>A; p.S247S; 6:20482777-20482777

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1169G>T; p.C390F; 6:20490201-20490201

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.524delA; p.T177fs*18; 6:20481224-20481224

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.513A>G; p.K171K; 6:20481213-20481213

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.694_696delAAG; p.K234delK; 6:20481394-20481396

large_intestine; coloncarcinoma; adenocarcinomaDeletion - In frame

c.1263G>A; p.P421P; 6:20490295-20490295

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.1263G>A; p.P421P; 6:20490295-20490295

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.1209A>T; p.P403P; 6:20490241-20490241

livercarcinomaSubstitution - coding silent

c.752G>A; p.G251D; 6:20482788-20482788

livercarcinomaSubstitution - Missense

c.752G>A; p.G251D; 6:20482788-20482788

livercarcinomaSubstitution - Missense

c.550G>T; p.G184C; 6:20481250-20481250

lungcarcinoma; non_small_cell_carcinomaSubstitution - Missense

c.914G>A; p.R305Q; 6:20486718-20486718

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.778T>A; p.S260T; 6:20482814-20482814

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.1116C>T; p.I372I; 6:20488229-20488229

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.1031G>T; p.G344V; 6:20488144-20488144

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1126G>A; p.A376T; 6:20488239-20488239

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.936C>A; p.D312E; 6:20486740-20486740

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1387A>G; p.M463V; 6:20490419-20490419

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1034C>G; p.P345R; 6:20488147-20488147

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1283C>T; p.P428L; 6:20490315-20490315

oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1201G>T; p.A401S; 6:20490233-20490233

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.893A>G; p.Y298C; 6:20486697-20486697

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.1305C>T; p.L435L; 6:20490337-20490337

skinmalignant_melanomaSubstitution - coding silent

c.1282C>T; p.P428S; 6:20490314-20490314

skinmalignant_melanomaSubstitution - Missense

c.1369C>T; p.P457S; 6:20490401-20490401

skinmalignant_melanomaSubstitution - Missense

c.798C>T; p.L266L; 6:20482834-20482834

skinmalignant_melanomaSubstitution - coding silent

c.1252C>T; p.L418L; 6:20490284-20490284

skinmalignant_melanomaSubstitution - coding silent

c.58G>A; p.E20K; 6:20402290-20402290

skinmalignant_melanomaSubstitution - Missense

c.1243C>T; p.P415S; 6:20490275-20490275

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1243C>T; p.P415S; 6:20490275-20490275

skinmalignant_melanomaSubstitution - Missense

c.1261_1262CC>TT; p.P421L; 6:20490293-20490294

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1195C>T; p.P399S; 6:20490227-20490227

skinmalignant_melanomaSubstitution - Missense

c.1124C>T; p.P375L; 6:20488237-20488237

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.864C>T; p.T288T; 6:20482900-20482900

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.485G>A; p.R162Q; 6:20479937-20479937

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.810G>A; p.E270E; 6:20482846-20482846

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.74T>C; p.V25A; 6:20402306-20402306

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.714C>T; p.N238N; 6:20481414-20481414

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.714C>T; p.N238N; 6:20481414-20481414

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1224G>A; p.Q408Q; 6:20490256-20490256

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.78C>T; p.A26A; 6:20402310-20402310

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.84C>A; p.A28A; 6:20402316-20402316

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.680G>T; p.G227V; 6:20481380-20481380

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1312C>A; p.L438I; 6:20490344-20490344

thyroidother; neoplasmSubstitution - Missense

c.147C>T; p.A49A; 6:20402379-20402379

thyroidcarcinomaSubstitution - coding silent

c.147C>T; p.A49A; 6:20402379-20402379

thyroidcarcinomaSubstitution - coding silent

c.952G>T; p.V318L; 6:20486756-20486756

thyroidcarcinomaSubstitution - Missense

c.1142C>A; p.A381D; 6:20490174-20490174

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1154C>G; p.S385*; 6:20490186-20490186

urinary_tract; bladdercarcinomaSubstitution - Nonsense