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

Basic Information

Gene ID

1435

Name

CSF1

Synonymous

colony stimulating factor 1 (macrophage);CSF1;colony stimulating factor 1 (macrophage)

Definition

lanimostim|macrophage colony-stimulating factor 1

Position

1p13.3

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.1358C>A; p.A453E; 1:109923979-109923979

autonomic_ganglianeuroblastomaSubstitution - Missense

c.634G>A; p.A212T; 1:109923255-109923255

autonomic_ganglianeuroblastomaSubstitution - Missense

c.1308C>T; p.P436P; 1:109923929-109923929

bone; pelvisEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.606G>A; p.P202P; 1:109923227-109923227

breastcarcinomaSubstitution - coding silent

c.1259C>G; p.S420C; 1:109923880-109923880

breastcarcinomaSubstitution - Missense

c.211G>C; p.D71H; 1:109915682-109915682

breastcarcinomaSubstitution - Missense

c.830C>T; p.S277L; 1:109923451-109923451

breastcarcinomaSubstitution - Missense

c.1158G>C; p.K386N; 1:109923779-109923779

breastcarcinomaSubstitution - Missense

c.795G>T; p.E265D; 1:109923416-109923416

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.293G>A; p.R98H; 1:109917360-109917360

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1245C>A; p.N415K; 1:109923866-109923866

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1236C>T; p.G412G; 1:109923857-109923857

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.774C>T; p.C258C; 1:109923395-109923395

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.262C>A; p.L88M; 1:109917329-109917329

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1501C>A; p.L501M; 1:109924122-109924122

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1408C>T; p.R470C; 1:109924029-109924029

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.301G>A; p.D101N; 1:109917368-109917368

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1529T>A; p.L510Q; 1:109924150-109924150

haematopoietic_and_lymphoid_tissue; small_intestinelymphoid_neoplasm; enteropathy_type_T_cell_lymphomaSubstitution - Missense

c.1312G>A; p.G438R; 1:109923933-109923933

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.959G>A; p.G320E; 1:109923580-109923580

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.292C>T; p.R98C; 1:109917359-109917359

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1562G>T; p.R521M; 1:109924183-109924183

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.205T>C; p.F69L; 1:109915676-109915676

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1095C>A; p.T365T; 1:109923716-109923716

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1229C>A; p.P410H; 1:109923850-109923850

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.686C>G; p.T229S; 1:109923307-109923307

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.420G>A; p.E140E; 1:109921870-109921870

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.409A>C; p.T137P; 1:109921859-109921859

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1513G>T; p.V505F; 1:109924134-109924134

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1420G>A; p.V474I; 1:109924041-109924041

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.781T>G; p.F261V; 1:109923402-109923402

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.184T>C; p.S62P; 1:109915655-109915655

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.184T>C; p.S62P; 1:109915655-109915655

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.321C>T; p.I107I; 1:109917388-109917388

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.322G>A; p.A108T; 1:109917389-109917389

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.486G>T; p.K162N; 1:109921936-109921936

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.486G>T; p.K162N; 1:109921936-109921936

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.486G>T; p.K162N; 1:109921936-109921936

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.545-7C>A; p.?; 1:109923159-109923159

large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.1212G>T; p.R404S; 1:109923833-109923833

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.947C>A; p.P316H; 1:109923568-109923568

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.791C>A; p.P264Q; 1:109923412-109923412

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1409G>A; p.R470H; 1:109924030-109924030

livercarcinomaSubstitution - Missense

c.1409G>A; p.R470H; 1:109924030-109924030

livercarcinomaSubstitution - Missense

c.1346G>T; p.R449L; 1:109923967-109923967

livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.1223T>C; p.L408P; 1:109923844-109923844

livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.905A>G; p.N302S; 1:109923526-109923526

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.973C>T; p.P325S; 1:109923594-109923594

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.926_930delCTGGA; p.S309fs*1; 1:109923547-109923551

lungcarcinoma; adenocarcinomaDeletion - Frameshift

c.372C>A; p.T124T; 1:109917439-109917439

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.80C>T; p.A27V; 1:109914299-109914299

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.980G>T; p.R327M; 1:109923601-109923601

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.688G>A; p.E230K; 1:109923309-109923309

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1193C>T; p.P398L; 1:109923814-109923814

oesophagus; lower_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.755G>A; p.R252Q; 1:109923376-109923376

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.403G>A; p.V135I; 1:109921853-109921853

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.1344T>G; p.D448E; 1:109923965-109923965

pancreascarcinomaSubstitution - Missense

c.157C>A; p.R53R; 1:109914376-109914376

prostatecarcinomaSubstitution - coding silent

c.1471C>T; p.P491S; 1:109924092-109924092

skinmalignant_melanomaSubstitution - Missense

c.131G>A; p.G44E; 1:109914350-109914350

skinmalignant_melanomaSubstitution - Missense

c.588C>T; p.A196A; 1:109923209-109923209

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.826G>A; p.G276S; 1:109923447-109923447

skinmalignant_melanomaSubstitution - Missense

c.647C>T; p.A216V; 1:109923268-109923268

skinmalignant_melanomaSubstitution - Missense

c.1190C>T; p.P397L; 1:109923811-109923811

skinmalignant_melanomaSubstitution - Missense

c.639C>T; p.P213P; 1:109923260-109923260

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1345C>T; p.R449W; 1:109923966-109923966

skinmalignant_melanomaSubstitution - Missense

c.1538G>A; p.G513E; 1:109924159-109924159

skinmalignant_melanomaSubstitution - Missense

c.958G>A; p.G320R; 1:109923579-109923579

skinmalignant_melanomaSubstitution - Missense

c.607G>T; p.A203S; 1:109923228-109923228

skinmalignant_melanomaSubstitution - Missense

c.615C>T; p.V205V; 1:109923236-109923236

skinmalignant_melanomaSubstitution - coding silent

c.591C>T; p.I197I; 1:109923212-109923212

skinmalignant_melanomaSubstitution - coding silent

c.1207C>T; p.P403S; 1:109923828-109923828

skinmalignant_melanomaSubstitution - Missense

c.149C>T; p.S50F; 1:109914368-109914368

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.471G>A; p.K157K; 1:109921921-109921921

skinmalignant_melanomaSubstitution - coding silent

c.629C>T; p.P210L; 1:109923250-109923250

skinmalignant_melanomaSubstitution - Missense

c.355C>T; p.L119L; 1:109917422-109917422

skinmalignant_melanomaSubstitution - coding silent

c.586G>A; p.A196T; 1:109923207-109923207

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1229C>T; p.P410L; 1:109923850-109923850

skin; scalpcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.854G>A; p.G285E; 1:109923475-109923475

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1151C>T; p.P384L; 1:109923772-109923772

skinmalignant_melanomaSubstitution - Missense

c.1601C>A; p.P534H; 1:109924807-109924807

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1139G>A; p.W380*; 1:109923760-109923760

skinmalignant_melanomaSubstitution - Nonsense

c.1648G>A; p.V550M; 1:109925172-109925172

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.253G>A; p.A85T; 1:109917320-109917320

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1419C>T; p.S473S; 1:109924040-109924040

stomachadenocarcinomaSubstitution - coding silent

c.822C>T; p.I274I; 1:109923443-109923443

upper_aerodigestive_tract; larynxcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.126G>A; p.M42I; 1:109914345-109914345

urinary_tract; bladdercarcinomaSubstitution - Missense

c.853G>A; p.G285R; 1:109923474-109923474

urinary_tract; bladdercarcinomaSubstitution - Missense

c.1194G>A; p.P398P; 1:109923815-109923815

urinary_tract; bladdercarcinomaSubstitution - coding silent