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

Basic Information

Gene ID

1875

Name

E2F5

Synonymous

E2F transcription factor 5, p130-binding;E2F5;E2F transcription factor 5, p130-binding

Definition

transcription factor E2F5

Position

8q21.2

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.662C>A; p.S221*; 8:85209188-85209188

adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningSubstitution - Nonsense

c.779T>C; p.V260A; 8:85209305-85209305

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.847G>A; p.A283T; 8:85209373-85209373

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.235-1G>T; p.?; 8:85202146-85202146

endometriumcarcinoma; endometrioid_carcinomaUnknown

c.506G>T; p.R169I; 8:85203255-85203255

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.633G>T; p.K211N; 8:85209159-85209159

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.610G>T; p.E204*; 8:85207484-85207484

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.534C>T; p.I178I; 8:85206204-85206204

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.513C>A; p.S171S; 8:85206183-85206183

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.581C>A; p.S194Y; 8:85207455-85207455

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.314delA; p.K107fs*11; 8:85202226-85202226

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.314delA; p.K107fs*11; 8:85202226-85202226

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.286A>G; p.N96D; 8:85202198-85202198

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.853C>T; p.Q285*; 8:85209379-85209379

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.635A>C; p.K212T; 8:85209161-85209161

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.712C>T; p.P238S; 8:85209238-85209238

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.489C>T; p.D163D; 8:85203238-85203238

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.615delG; p.G206fs*12; 8:85207489-85207489

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.132C>G; p.A44A; 8:85177552-85177552

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.941T>C; p.L314P; 8:85213762-85213762

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.941T>C; p.L314P; 8:85213762-85213762

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.941T>C; p.L314P; 8:85213762-85213762

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.260delA; p.R89fs*10; 8:85202172-85202172

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.906C>A; p.I302I; 8:85212179-85212179

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.131delC; p.G46fs*40; 8:85177551-85177551

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.838A>T; p.R280*; 8:85209364-85209364

livercarcinomaSubstitution - Nonsense

c.838A>T; p.R280*; 8:85209364-85209364

livercarcinomaSubstitution - Nonsense

c.529G>A; p.D177N; 8:85206199-85206199

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.342G>T; p.W114C; 8:85202254-85202254

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.906C>T; p.I302I; 8:85212179-85212179

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.727G>A; p.V243I; 8:85209253-85209253

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.289G>T; p.V97F; 8:85202201-85202201

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.291C>G; p.V97V; 8:85202203-85202203

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.479A>T; p.N160I; 8:85203228-85203228

NSNSSubstitution - Missense

c.260delA; p.R89fs*10; 8:85202172-85202172

oesophagus; lower_thirdcarcinoma; adenocarcinomaDeletion - Frameshift

c.908T>C; p.I303T; 8:85212181-85212181

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.941T>A; p.L314H; 8:85213762-85213762

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.709A>T; p.K237*; 8:85209235-85209235

ovarycarcinoma; serous_carcinomaSubstitution - Nonsense

c.884-3C>T; p.?; 8:85212154-85212154

ovaryother; neoplasmUnknown

c.752A>C; p.Q251P; 8:85209278-85209278

pancreascarcinomaSubstitution - Missense

c.752A>C; p.Q251P; 8:85209278-85209278

pancreascarcinomaSubstitution - Missense

c.752A>C; p.Q251P; 8:85209278-85209278

pancreascarcinomaSubstitution - Missense

c.429G>A; p.K143K; 8:85203178-85203178

skinmalignant_melanomaSubstitution - coding silent

c.560delT; p.L188fs*30; 8:85207434-85207434

skin; backmalignant_melanomaDeletion - Frameshift

c.899G>A; p.G300E; 8:85212172-85212172

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.255G>A; p.V85V; 8:85202167-85202167

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.785C>T; p.P262L; 8:85209311-85209311

skinmalignant_melanomaSubstitution - Missense

c.947G>A; p.R316K; 8:85213768-85213768

skinmalignant_melanomaSubstitution - Missense

c.947G>A; p.R316K; 8:85213768-85213768

skinmalignant_melanomaSubstitution - Missense

c.719_720insT; p.P242fs*6; 8:85209245-85209246

stomachcarcinoma; intestinal_adenocarcinomaInsertion - Frameshift

c.675T>C; p.H225H; 8:85209201-85209201

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.753G>A; p.Q251Q; 8:85209279-85209279

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.132C>G; p.A44A; 8:85177552-85177552

thyroidother; neoplasmSubstitution - coding silent

c.132C>G; p.A44A; 8:85177552-85177552

thyroidother; neoplasmSubstitution - coding silent

c.132C>G; p.A44A; 8:85177552-85177552

thyroidother; neoplasmSubstitution - coding silent

c.662C>T; p.S221L; 8:85209188-85209188

urinary_tract; bladdercarcinomaSubstitution - Missense