| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 7031 |
Name | TFF1 |
Synonymous | trefoil factor 1;TFF1;trefoil factor 1 |
Definition | breast cancer estrogen-inducible protein|breast cancer estrogen-inducible sequence|gastrointestinal trefoil protein pS2|polypeptide P1.A|protein pS2 |
Position | 21q22.3 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.121T>A; p.C41S; 21:42363372-42363372 |
liver | carcinoma | Substitution - Missense |
c.157A>C; p.N53H; 21:42363336-42363336 |
pancreas | pancreatic_intraepithelial_neoplasia_(PanIN) | Substitution - Missense |
c.157A>C; p.N53H; 21:42363336-42363336 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.129T>C; p.F43F; 21:42363364-42363364 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.153_154delTG; p.A52fs*2; 21:42363339-42363340 |
liver | carcinoma; hepatocellular_carcinoma | Deletion - Frameshift |
c.223G>A; p.D75N; 21:42363270-42363270 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.130C>T; p.P44S; 21:42363363-42363363 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.47C>T; p.S16F; 21:42366449-42366449 |
skin | malignant_melanoma | Substitution - Missense |
c.117G>A; p.Q39Q; 21:42363376-42363376 |
skin | malignant_melanoma | Substitution - coding silent |
c.174C>T; p.F58F; 21:42363319-42363319 |
skin | malignant_melanoma | Substitution - coding silent |
c.174C>T; p.F58F; 21:42363319-42363319 |
skin | malignant_melanoma | Substitution - coding silent |
c.231T>C; p.P77P; 21:42363262-42363262 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.131C>T; p.P44L; 21:42363362-42363362 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.76G>A; p.A26T; 21:42366420-42366420 |
skin | malignant_melanoma | Substitution - Missense |
c.165C>A; p.G55G; 21:42363328-42363328 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.190G>T; p.G64W; 21:42363303-42363303 |
kidney | other; neoplasm | Substitution - Missense |
c.46T>C; p.S16P; 21:42366450-42366450 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.46T>C; p.S16P; 21:42366450-42366450 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.148C>T; p.Q50*; 21:42363345-42363345 |
skin | malignant_melanoma | Substitution - Nonsense |
c.6C>T; p.A2A; 21:42366490-42366490 |
skin | malignant_melanoma | Substitution - coding silent |
c.49A>G; p.M17V; 21:42366447-42366447 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.36_37GG>AA; p.V13I; 21:42366459-42366460 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.60C>T; p.L20L; 21:42366436-42366436 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.195_196CC>TT; p.P66S; 21:42363297-42363298 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |