| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 1487 | ||
Name | CTBP1 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.570G>A; p.A190A; 4:1216183-1216183 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.326C>T; p.S109L; 4:1228213-1228213 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1287C>G; p.P429P; 4:1212276-1212276 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.159C>T; p.F53F; 4:1238219-1238219 |
breast | carcinoma | Substitution - coding silent |
c.811G>A; p.D271N; 4:1214425-1214425 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.41-7C>T; p.?; 4:1238344-1238344 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Unknown |
c.140A>G; p.D47G; 4:1238238-1238238 |
skin | malignant_melanoma | Substitution - Missense |
c.640_641insAG; p.A214fs*21; 4:1216112-1216113 |
pancreas | pancreatic_intraepithelial_neoplasia_(PanIN) | Insertion - Frameshift |
c.1047C>G; p.N349K; 4:1213005-1213005 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1089C>T; p.A363A; 4:1212963-1212963 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.289C>T; p.R97W; 4:1228250-1228250 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.570G>T; p.A190A; 4:1216183-1216183 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1125T>G; p.N375K; 4:1212927-1212927 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.796C>T; p.R266W; 4:1214440-1214440 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.174C>T; p.S58S; 4:1238204-1238204 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.179A>T; p.Q60L; 4:1238199-1238199 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1320G>T; p.L440F; 4:1212243-1212243 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.205G>A; p.E69K; 4:1228334-1228334 |
breast | carcinoma | Substitution - Missense |
c.1108G>T; p.V370L; 4:1212944-1212944 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.943delC; p.H315fs*33; 4:1213556-1213556 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.209C>T; p.A70V; 4:1228330-1228330 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.858C>T; p.G286G; 4:1214378-1214378 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.960C>T; p.S320S; 4:1213539-1213539 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.553G>T; p.V185L; 4:1216200-1216200 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1257C>T; p.H419H; 4:1212306-1212306 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1148C>T; p.P383L; 4:1212415-1212415 |
pancreas | carcinoma | Substitution - Missense |
c.308A>T; p.D103V; 4:1228231-1228231 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.575G>A; p.R192Q; 4:1216178-1216178 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.795C>T; p.A265A; 4:1214441-1214441 |
skin | malignant_melanoma | Substitution - coding silent |
c.267C>T; p.F89F; 4:1228272-1228272 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1167C>G; p.A389A; 4:1212396-1212396 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.827C>T; p.A276V; 4:1214409-1214409 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.518G>A; p.R173H; 4:1225389-1225389 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.794C>T; p.A265V; 4:1214442-1214442 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.997C>T; p.R333W; 4:1213502-1213502 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.965A>G; p.Q322R; 4:1213534-1213534 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1120C>T; p.L374F; 4:1212932-1212932 |
thyroid | carcinoma | Substitution - Missense |
c.853C>T; p.R285C; 4:1214383-1214383 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.637C>T; p.R213W; 4:1216116-1216116 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.331G>A; p.G111R; 4:1228208-1228208 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.111C>T; p.D37D; 4:1238267-1238267 |
pancreas | carcinoma | Substitution - coding silent |
c.148A>G; p.T50A; 4:1238230-1238230 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.711C>T; p.C237C; 4:1216042-1216042 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.166G>A; p.A56T; 4:1238212-1238212 |
liver | carcinoma | Substitution - Missense |
c.176C>T; p.T59M; 4:1238202-1238202 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.425G>A; p.R142Q; 4:1225482-1225482 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.603C>A; p.L201L; 4:1216150-1216150 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1153G>A; p.V385M; 4:1212410-1212410 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1048T>G; p.C350G; 4:1213004-1213004 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.610G>A; p.D204N; 4:1216143-1216143 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.610G>A; p.D204N; 4:1216143-1216143 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.610G>A; p.D204N; 4:1216143-1216143 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.610G>A; p.D204N; 4:1216143-1216143 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.844G>T; p.G282C; 4:1214392-1214392 |
liver | carcinoma | Substitution - Missense |
c.844G>T; p.G282C; 4:1214392-1214392 |
liver | carcinoma | Substitution - Missense |
c.205G>T; p.E69*; 4:1228334-1228334 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.365C>T; p.A122V; 4:1225542-1225542 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1053C>T; p.V351V; 4:1212999-1212999 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.784G>A; p.V262M; 4:1214452-1214452 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.923C>A; p.P308H; 4:1213576-1213576 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1083C>T; p.H361H; 4:1212969-1212969 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1161C>T; p.G387G; 4:1212402-1212402 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.920C>T; p.A307V; 4:1213579-1213579 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.107G>A; p.R36Q; 4:1238271-1238271 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.935G>T; p.C312F; 4:1213564-1213564 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |