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

Basic Information

Gene ID

929

Name

CD14

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.4G>A; p.E2K; 5:140632980-140632980

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.4G>A; p.E2K; 5:140632980-140632980

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.339A>T; p.L113L; 5:140632645-140632645

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.370G>C; p.E124Q; 5:140632614-140632614

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.374A>G; p.D125G; 5:140632610-140632610

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.883delC; p.L295fs*15; 5:140632101-140632101

 breastcarcinoma; ductal_carcinomaDeletion - Frameshift

c.989C>T; p.P330L; 5:140631995-140631995

 skinmalignant_melanomaSubstitution - Missense

c.784C>T; p.R262C; 5:140632200-140632200

 peritoneum; appendixother; pseudomyxoma_peritoneiSubstitution - Missense

c.322G>A; p.G108S; 5:140632662-140632662

 oesophagus; middle_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.932G>T; p.R311M; 5:140632052-140632052

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.127C>A; p.P43T; 5:140632857-140632857

 breastcarcinomaSubstitution - Missense

c.414A>G; p.E138E; 5:140632570-140632570

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.875C>A; p.P292H; 5:140632109-140632109

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1099C>A; p.L367M; 5:140631885-140631885

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.18C>G; p.C6W; 5:140632966-140632966

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.562G>T; p.E188*; 5:140632422-140632422

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.526A>C; p.S176R; 5:140632458-140632458

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.494A>G; p.Q165R; 5:140632490-140632490

 pancreasother; adenomaSubstitution - Missense

c.887C>A; p.P296Q; 5:140632097-140632097

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.499T>C; p.W167R; 5:140632485-140632485

 livercarcinomaSubstitution - Missense

c.851C>T; p.S284L; 5:140632133-140632133

 skinmalignant_melanomaSubstitution - Missense

c.499T>C; p.W167R; 5:140632485-140632485

 livercarcinomaSubstitution - Missense

c.37C>T; p.P13S; 5:140632947-140632947

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.514C>T; p.L172F; 5:140632470-140632470

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.673C>T; p.Q225*; 5:140632311-140632311

 skinmalignant_melanomaSubstitution - Nonsense

c.708G>A; p.T236T; 5:140632276-140632276

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1038C>A; p.S346S; 5:140631946-140631946

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.844A>C; p.N282H; 5:140632140-140632140

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.180T>C; p.H60H; 5:140632804-140632804

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.301G>C; p.V101L; 5:140632683-140632683

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.147C>T; p.F49F; 5:140632837-140632837

 skinmalignant_melanomaSubstitution - coding silent

c.577T>G; p.F193V; 5:140632407-140632407

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1020C>A; p.H340Q; 5:140631964-140631964

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.63G>A; p.T21T; 5:140632921-140632921

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphomaSubstitution - coding silent

c.910C>A; p.L304I; 5:140632074-140632074

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.641C>T; p.A214V; 5:140632343-140632343

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.56C>A; p.A19E; 5:140632928-140632928

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.779C>G; p.S260W; 5:140632205-140632205

 bone; extraskeletalEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.1064C>T; p.S355L; 5:140631920-140631920

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.852G>A; p.S284S; 5:140632132-140632132

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.852G>A; p.S284S; 5:140632132-140632132

 skinmalignant_melanomaSubstitution - coding silent

c.639G>A; p.M213I; 5:140632345-140632345

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1049C>A; p.P350Q; 5:140631935-140631935

 soft_tissue; striated_musclerhabdomyosarcoma; alveolarSubstitution - Missense

c.808C>T; p.P270S; 5:140632176-140632176

 skinmalignant_melanomaSubstitution - Missense

c.648_649delCT; p.C217fs*51; 5:140632335-140632336

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.855C>T; p.F285F; 5:140632129-140632129

 skinmalignant_melanomaSubstitution - coding silent

c.1108G>A; p.G370R; 5:140631876-140631876

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.439T>G; p.L147V; 5:140632545-140632545

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.561C>T; p.C187C; 5:140632423-140632423

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.860G>A; p.G287E; 5:140632124-140632124

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.860G>A; p.G287E; 5:140632124-140632124

 upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.961G>A; p.V321M; 5:140632023-140632023

 skinmalignant_melanomaSubstitution - Missense

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