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

Basic Information

Gene ID

3068

Name

HDGF

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.465G>A; p.K155K; 1:156744187-156744187

 breastcarcinomaSubstitution - coding silent

c.363T>C; p.G121G; 1:156744289-156744289

 livercarcinomaSubstitution - coding silent

c.612C>T; p.P204P; 1:156743756-156743756

 bone; extraskeletalEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.165-1_165insAC; p.A56fs*100; 1:156745146-156745147

 large_intestinecarcinoma; adenocarcinomaUnknown

c.149delT; p.F50fs*105; 1:156745312-156745312

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.196T>G; p.Y66D; 1:156745115-156745115

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.149delT; p.F50fs*105; 1:156745312-156745312

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.149delT; p.F50fs*105; 1:156745312-156745312

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.349G>A; p.E117K; 1:156744303-156744303

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.149delT; p.F50fs*105; 1:156745312-156745312

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.149delT; p.F50fs*105; 1:156745312-156745312

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.149delT; p.F50fs*105; 1:156745312-156745312

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.149delT; p.F50fs*105; 1:156745312-156745312

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.88-1_92delGATTGA; p.?; 1:156745369-156745374

 livercarcinoma; hepatocellular_carcinomaUnknown

c.52G>A; p.A18T; 1:156751378-156751378

 oesophaguscarcinomaSubstitution - Missense

c.178C>T; p.P60S; 1:156745133-156745133

 skinmalignant_melanomaSubstitution - Missense

c.174G>A; p.L58L; 1:156745137-156745137

 oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.198C>A; p.Y66*; 1:156745113-156745113

 lungcarcinoma; non_small_cell_carcinomaSubstitution - Nonsense

c.602C>T; p.P201L; 1:156743766-156743766

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.236G>C; p.R79T; 1:156745075-156745075

 stomachadenocarcinomaSubstitution - Missense

c.386C>T; p.A129V; 1:156744266-156744266

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.196T>C; p.Y66H; 1:156745115-156745115

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.308C>A; p.S103Y; 1:156744344-156744344

 skinmalignant_melanomaSubstitution - Missense

c.364G>A; p.D122N; 1:156744288-156744288

 upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.364G>A; p.D122N; 1:156744288-156744288

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.308C>T; p.S103F; 1:156744344-156744344

 skinmalignant_melanomaSubstitution - Missense

c.45G>C; p.L15L; 1:156751385-156751385

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.295G>A; p.G99S; 1:156745016-156745016

 haematopoietic_and_lymphoid_tissue; spleenlymphoid_neoplasm; marginal_zone_lymphomaSubstitution - Missense

c.458C>T; p.A153V; 1:156744194-156744194

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.453A>G; p.K151K; 1:156744199-156744199

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.541G>C; p.E181Q; 1:156743827-156743827

 bone; scapulaEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.341C>A; p.P114Q; 1:156744311-156744311

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.455G>T; p.G152V; 1:156744197-156744197

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.294C>T; p.S98S; 1:156745017-156745017

 bone; extraskeletalEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.290C>T; p.A97V; 1:156745021-156745021

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.267C>G; p.I89M; 1:156745044-156745044

 oesophaguscarcinomaSubstitution - Missense

c.87+2T>G; p.?; 1:156751341-156751341

 breastcarcinomaUnknown

c.149_150insT; p.G51fs*63; 1:156745311-156745312

 large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.149_150insT; p.G51fs*63; 1:156745311-156745312

 large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.149_150insT; p.G51fs*63; 1:156745311-156745312

 large_intestinecarcinoma; adenocarcinomaInsertion - Frameshift

c.505C>T; p.P169S; 1:156743863-156743863

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.459G>A; p.A153A; 1:156744193-156744193

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.198C>T; p.Y66Y; 1:156745113-156745113

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.198C>T; p.Y66Y; 1:156745113-156745113

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.486G>A; p.L162L; 1:156744166-156744166

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.164+1G>T; p.?; 1:156745296-156745296

 bone; femurchondrosarcomaUnknown

c.564G>A; p.E188E; 1:156743804-156743804

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.403G>A; p.E135K; 1:156744249-156744249

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; plasma_cell_myelomaSubstitution - Missense

c.385G>T; p.A129S; 1:156744267-156744267

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.197A>G; p.Y66C; 1:156745114-156745114

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.303+6C>A; p.?; 1:156745002-156745002

 stomachadenocarcinomaUnknown

c.649G>A; p.E217K; 1:156743719-156743719

 livercarcinomaSubstitution - Missense

c.649G>A; p.E217K; 1:156743719-156743719

 livercarcinomaSubstitution - Missense

c.553T>C; p.L185L; 1:156743815-156743815

 pancreascarcinomaSubstitution - coding silent

c.400G>A; p.D134N; 1:156744252-156744252

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.526G>A; p.E176K; 1:156743842-156743842

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.199G>A; p.E67K; 1:156745112-156745112

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.654_656delGGA; p.E218delE; 1:156743712-156743714

 endometriumcarcinoma; endometrioid_carcinomaDeletion - In frame

c.529G>A; p.G177R; 1:156743839-156743839

 bone; extraskeletalEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.241G>A; p.G81R; 1:156745070-156745070

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.623G>A; p.R208Q; 1:156743745-156743745

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.427G>T; p.E143*; 1:156744225-156744225

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.402C>T; p.D134D; 1:156744250-156744250

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.613G>A; p.G205S; 1:156743755-156743755

 kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

')