Cancer metastasis gene database Home
Cancer metastasis database
General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

7023

Name

TFAP4

Synonymous

transcription factor AP-4 (activating enhancer binding protein 4);TFAP4;transcription factor AP-4 (activating enhancer binding protein 4)

Definition

activating enhancer-binding protein 4|class C basic helix-loop-helix protein 41|transcription factor AP-4|transcription factor AP-4 (activating enhancer-binding protein 4)

Position

16p13

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.364G>A; p.G122S; 16:4261940-4261940

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.812C>T; p.T271I; 16:4260100-4260100

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.842G>T; p.G281V; 16:4258230-4258230

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.169G>A; p.E57K; 16:4262622-4262622

skinmalignant_melanomaSubstitution - Missense

c.774C>T; p.V258V; 16:4260138-4260138

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.348C>T; p.F116F; 16:4262330-4262330

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.61G>A; p.E21K; 16:4272686-4272686

NSNSSubstitution - Missense

c.172C>T; p.R58W; 16:4262619-4262619

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.172C>T; p.R58W; 16:4262619-4262619

haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - Missense

c.738C>T; p.H246H; 16:4260174-4260174

boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.156C>T; p.I52I; 16:4262635-4262635

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.737A>G; p.H246R; 16:4260175-4260175

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.371C>T; p.S124F; 16:4261933-4261933

skinmalignant_melanomaSubstitution - Missense

c.705G>A; p.V235V; 16:4260207-4260207

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.288C>A; p.I96I; 16:4262390-4262390

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.973G>T; p.D325Y; 16:4258099-4258099

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.816C>T; p.I272I; 16:4260096-4260096

skinmalignant_melanomaSubstitution - coding silent

c.771G>A; p.S257S; 16:4260141-4260141

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.340A>G; p.K114E; 16:4262338-4262338

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.654G>C; p.Q218H; 16:4260467-4260467

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1004G>A; p.G335E; 16:4258068-4258068

large_intestine; coloncarcinomaSubstitution - Missense

c.654G>C; p.Q218H; 16:4260467-4260467

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.179G>A; p.R60H; 16:4262612-4262612

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.179G>A; p.R60H; 16:4262612-4262612

prostatecarcinomaSubstitution - Missense

c.179G>A; p.R60H; 16:4262612-4262612

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.179G>A; p.R60H; 16:4262612-4262612

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.679C>T; p.P227S; 16:4260233-4260233

breastcarcinomaSubstitution - Missense

c.140G>A; p.R47Q; 16:4262651-4262651

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.267C>T; p.L89L; 16:4262411-4262411

skin; trunkmalignant_melanoma; nodularSubstitution - coding silent

c.238G>A; p.G80R; 16:4262553-4262553

oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.878G>A; p.R293Q; 16:4258194-4258194

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.417C>T; p.S139S; 16:4261887-4261887

skinmalignant_melanomaSubstitution - coding silent

c.145C>T; p.R49W; 16:4262646-4262646

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.352C>T; p.Q118*; 16:4262326-4262326

skinmalignant_melanomaSubstitution - Nonsense

c.71T>C; p.V24A; 16:4272676-4272676

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.730C>T; p.P244S; 16:4260182-4260182

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.770C>A; p.S257*; 16:4260142-4260142

lungcarcinoma; adenocarcinomaSubstitution - Nonsense

c.874C>G; p.Q292E; 16:4258198-4258198

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.173G>A; p.R58Q; 16:4262618-4262618

haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - Missense

c.590T>A; p.L197Q; 16:4260531-4260531

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.136C>T; p.R46W; 16:4262655-4262655

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.842G>A; p.G281D; 16:4258230-4258230

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1006G>C; p.E336Q; 16:4258066-4258066

lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.89G>T; p.S30I; 16:4272658-4272658

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.194A>G; p.N65S; 16:4262597-4262597

breastcarcinomaSubstitution - Missense

c.222C>A; p.L74L; 16:4262569-4262569

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.750C>T; p.V250V; 16:4260162-4260162

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.280G>A; p.E94K; 16:4262398-4262398

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.237C>T; p.D79D; 16:4262554-4262554

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.293C>T; p.S98F; 16:4262385-4262385

skinmalignant_melanomaSubstitution - Missense

c.880C>T; p.R294*; 16:4258192-4258192

stomachcarcinoma; adenocarcinomaSubstitution - Nonsense

c.744C>T; p.I248I; 16:4260168-4260168

skinmalignant_melanomaSubstitution - coding silent

c.148C>T; p.R50W; 16:4262643-4262643

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; Burkitt_lymphomaSubstitution - Missense

c.148C>T; p.R50W; 16:4262643-4262643

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemiaSubstitution - Missense

c.148C>T; p.R50W; 16:4262643-4262643

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.4G>T; p.E2*; 16:4272743-4272743

breastcarcinomaSubstitution - Nonsense

c.688A>C; p.T230P; 16:4260224-4260224

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.688A>C; p.T230P; 16:4260224-4260224

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.593A>T; p.Q198L; 16:4260528-4260528

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.688A>C; p.T230P; 16:4260224-4260224

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.688A>C; p.T230P; 16:4260224-4260224

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.688A>C; p.T230P; 16:4260224-4260224

lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.688A>C; p.T230P; 16:4260224-4260224

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.21C>A; p.P7P; 16:4272726-4272726

pancreascarcinomaSubstitution - coding silent

c.406G>A; p.G136S; 16:4261898-4261898

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.763C>T; p.P255S; 16:4260149-4260149

skinmalignant_melanomaSubstitution - Missense

c.760G>A; p.G254S; 16:4260152-4260152

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.883G>T; p.A295S; 16:4258189-4258189

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.454C>T; p.R152W; 16:4261850-4261850

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.611T>C; p.V204A; 16:4260510-4260510

pancreascarcinomaSubstitution - Missense

c.385C>T; p.R129W; 16:4261919-4261919

breastcarcinomaSubstitution - Missense

c.157G>A; p.A53T; 16:4262634-4262634

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense