| Gene ID | 2152 |
| Symbol | F3 |
| Synonymous | CD142|TF|TFA |
| Full name | coagulation factor III (thromboplastin, tissue factor) |
| Gene description | tissue factor |
| Cytoband | 1p22-p21 |
| Gene type | protein-coding |
| Synonymous | MIM:134390; HGNC:HGNC:3541; Ensembl:ENSG00000117525; HPRD:00603; Vega:OTTHUMG00000010716 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.823C>A; p.H275N; 1:94530525-94530525 |
kidney | other; neoplasm | Substitution - Missense |
c.426G>A; p.Q142Q; 1:94533255-94533255 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.529G>T; p.D177Y; 1:94533152-94533152 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.543G>A; p.K181K; 1:94533138-94533138 |
large_intestine; colon | NS | Substitution - coding silent |
c.872C>T; p.P291L; 1:94530476-94530476 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.682C>A; p.R228R; 1:94532390-94532390 |
skin | malignant_melanoma | Substitution - coding silent |
c.666A>C; p.Q222H; 1:94532406-94532406 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.713C>G; p.P238R; 1:94532359-94532359 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.692A>C; p.N231T; 1:94532380-94532380 |
skin | malignant_melanoma | Substitution - Missense |
c.449A>G; p.Q150R; 1:94533232-94533232 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.395T>G; p.F132C; 1:94535982-94535982 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.281A>G; p.E94G; 1:94536096-94536096 |
skin | malignant_melanoma | Substitution - Missense |
c.308A>C; p.Y103S; 1:94536069-94536069 |
NS | NS | Substitution - Missense |
c.881T>C; p.V294A; 1:94530467-94530467 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.475G>A; p.V159I; 1:94533206-94533206 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.699G>A; p.K233K; 1:94532373-94532373 |
skin | malignant_melanoma | Substitution - coding silent |
c.282G>A; p.E94E; 1:94536095-94536095 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.83A>G; p.Q28R; 1:94541554-94541554 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.316C>T; p.R106W; 1:94536061-94536061 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.316C>T; p.R106W; 1:94536061-94536061 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.316C>T; p.R106W; 1:94536061-94536061 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.539G>A; p.G180D; 1:94533142-94533142 |
skin | malignant_melanoma | Substitution - Missense |
c.37G>C; p.E13Q; 1:94541600-94541600 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.543G>T; p.K181N; 1:94533138-94533138 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.202_203delGT; p.V68fs*5; 1:94540266-94540267 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.327C>T; p.S109S; 1:94536050-94536050 |
skin | malignant_melanoma | Substitution - coding silent |
c.804C>A; p.I268I; 1:94530544-94530544 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.174A>G; p.E58E; 1:94540295-94540295 |
skin | malignant_melanoma | Substitution - coding silent |
c.354C>A; p.T118T; 1:94536023-94536023 |
breast | carcinoma | Substitution - coding silent |
c.810G>A; p.L270L; 1:94530538-94530538 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; essential_thrombocythaemia | Substitution - coding silent |
c.455G>A; p.G152E; 1:94533226-94533226 |
skin | malignant_melanoma | Substitution - Missense |
c.455G>A; p.G152E; 1:94533226-94533226 |
skin | malignant_melanoma | Substitution - Missense |
c.778G>A; p.V260I; 1:94530570-94530570 |
skin | malignant_melanoma | Substitution - Missense |
c.465G>C; p.V155V; 1:94533216-94533216 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.521G>A; p.S174N; 1:94533160-94533160 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4G>A; p.E2K; 1:94541633-94541633 |
skin | malignant_melanoma | Substitution - Missense |
c.465G>A; p.V155V; 1:94533216-94533216 |
skin | malignant_melanoma | Substitution - coding silent |
c.522C>G; p.S174R; 1:94533159-94533159 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.127A>G; p.N43D; 1:94540342-94540342 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.502A>C; p.R168R; 1:94533179-94533179 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.242G>T; p.C81F; 1:94536135-94536135 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.381G>T; p.E127D; 1:94535996-94535996 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.604delA; p.T202fs*7; 1:94532468-94532468 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.131T>G; p.L44*; 1:94540338-94540338 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.598G>A; p.A200T; 1:94532474-94532474 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |