| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 6932 | ||
Name | TCF7 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1095C>A; p.F365L; 5:134146243-134146243 |
liver | carcinoma | Substitution - Missense |
c.1095C>A; p.F365L; 5:134146243-134146243 |
liver | carcinoma | Substitution - Missense |
c.810G>T; p.K270N; 5:134142775-134142775 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.850A>G; p.R284G; 5:134142815-134142815 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.428C>T; p.P143L; 5:134116020-134116020 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.478_481delCTCT; p.L162fs*36; 5:134138095-134138098 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.983T>G; p.L328R; 5:134143057-134143057 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.229G>A; p.G77R; 5:134115135-134115135 |
thyroid | other; neoplasm | Substitution - Missense |
c.839T>C; p.M280T; 5:134142804-134142804 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.509A>T; p.H170L; 5:134138126-134138126 |
skin | malignant_melanoma | Substitution - Missense |
c.413G>A; p.G138E; 5:134116005-134116005 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.806T>C; p.I269T; 5:134142771-134142771 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.711_712insC; p.S240fs*55; 5:134142260-134142261 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.510T>C; p.H170H; 5:134138127-134138127 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.673C>G; p.P225A; 5:134142222-134142222 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1026+1G>A; p.?; 5:134143101-134143101 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.258G>T; p.G86G; 5:134115329-134115329 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.745G>A; p.D249N; 5:134142294-134142294 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1043G>A; p.R348Q; 5:134143608-134143608 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.490G>A; p.E164K; 5:134138107-134138107 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.490G>A; p.E164K; 5:134138107-134138107 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.490G>A; p.E164K; 5:134138107-134138107 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.742T>C; p.F248L; 5:134142291-134142291 |
liver | carcinoma | Substitution - Missense |
c.742T>C; p.F248L; 5:134142291-134142291 |
liver | carcinoma | Substitution - Missense |
c.965C>T; p.A322V; 5:134143039-134143039 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.786G>T; p.K262N; 5:134142751-134142751 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1131G>A; p.P377P; 5:134146279-134146279 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.492A>G; p.E164E; 5:134138109-134138109 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.487T>G; p.Y163D; 5:134138104-134138104 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemia | Substitution - Missense |
c.472C>T; p.P158S; 5:134138089-134138089 |
skin | malignant_melanoma | Substitution - Missense |
c.802A>T; p.T268S; 5:134142767-134142767 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.721G>T; p.G241W; 5:134142270-134142270 |
breast | carcinoma | Substitution - Missense |
c.927G>A; p.A309A; 5:134143001-134143001 |
pancreas | carcinoma | Substitution - coding silent |
c.447G>T; p.K149N; 5:134138064-134138064 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.261G>A; p.R87R; 5:134115332-134115332 |
skin | malignant_melanoma | Substitution - coding silent |
c.958G>A; p.E320K; 5:134143032-134143032 |
breast | carcinoma | Substitution - Missense |
c.612G>A; p.G204G; 5:134139015-134139015 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.457delC; p.H155fs*44; 5:134138074-134138074 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.457delC; p.H155fs*44; 5:134138074-134138074 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.457delC; p.H155fs*44; 5:134138074-134138074 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.457delC; p.H155fs*44; 5:134138074-134138074 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.420delC; p.Q142fs*57; 5:134116012-134116012 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.528G>A; p.A176A; 5:134138145-134138145 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.489C>T; p.Y163Y; 5:134138106-134138106 |
breast | carcinoma | Substitution - coding silent |
c.456_457insC; p.H155fs*37; 5:134138073-134138074 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.456_457insC; p.H155fs*37; 5:134138073-134138074 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.456_457insC; p.H155fs*37; 5:134138073-134138074 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.456_457insC; p.H155fs*37; 5:134138073-134138074 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.456_457insC; p.H155fs*37; 5:134138073-134138074 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.379C>A; p.L127M; 5:134115971-134115971 |
breast | carcinoma | Substitution - Missense |
c.832C>A; p.L278M; 5:134142797-134142797 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1046C>T; p.S349L; 5:134143611-134143611 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.370G>A; p.A124T; 5:134115962-134115962 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.928C>T; p.L310L; 5:134143002-134143002 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1106C>T; p.P369L; 5:134146254-134146254 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.619C>A; p.P207T; 5:134139022-134139022 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1047G>A; p.S349S; 5:134143612-134143612 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.405G>A; p.S135S; 5:134115997-134115997 |
breast | carcinoma | Substitution - coding silent |
c.1096G>A; p.G366S; 5:134146244-134146244 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.944A>T; p.Q315L; 5:134143018-134143018 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.397delC; p.S135fs*64; 5:134115989-134115989 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |