| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 7205 |
Name | TRIP6 |
Synonymous | thyroid hormone receptor interactor 6;TRIP6;thyroid hormone receptor interactor 6 |
Definition | OPA-interacting protein 1|TR-interacting protein 6|thyroid hormone receptor interacting protein 6|thyroid receptor-interacting protein 6|zyxin related protein 1 |
Position | 7q22 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1276C>T; p.H426Y; 7:100872721-100872721 |
breast | carcinoma | Substitution - Missense |
c.1384G>A; p.A462T; 7:100873256-100873256 |
breast | carcinoma | Substitution - Missense |
c.1375_1383delGCCTGCAGC; p.A459_S461delACS; 7:100873247-100873255 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Deletion - In frame |
c.767delT; p.L256fs*4; 7:100870401-100870401 |
breast | carcinoma | Deletion - Frameshift |
c.1096G>A; p.V366M; 7:100871639-100871639 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.398C>T; p.T133M; 7:100868529-100868529 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.883G>A; p.A295T; 7:100870627-100870627 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.342G>A; p.A114A; 7:100868212-100868212 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.834G>C; p.Q278H; 7:100870578-100870578 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1402C>T; p.L468F; 7:100873274-100873274 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.305G>T; p.S102I; 7:100868175-100868175 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.819G>T; p.G273G; 7:100870453-100870453 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.780G>A; p.T260T; 7:100870414-100870414 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1239G>T; p.E413D; 7:100872684-100872684 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1217T>C; p.I406T; 7:100872662-100872662 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.896T>C; p.V299A; 7:100870640-100870640 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1268G>A; p.R423Q; 7:100872713-100872713 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.495C>T; p.G165G; 7:100868626-100868626 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.730delC; p.Q245fs*4; 7:100868861-100868861 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1403T>C; p.L468P; 7:100873275-100873275 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.282C>T; p.D94D; 7:100868152-100868152 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1249A>T; p.R417*; 7:100872694-100872694 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1019C>T; p.A340V; 7:100871562-100871562 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.379C>T; p.P127S; 7:100868510-100868510 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.867T>C; p.D289D; 7:100870611-100870611 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.893G>A; p.R298H; 7:100870637-100870637 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.946G>A; p.G316S; 7:100870690-100870690 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1095C>T; p.C365C; 7:100871638-100871638 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1095C>T; p.C365C; 7:100871638-100871638 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.194G>T; p.G65V; 7:100867945-100867945 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.780G>A; p.T260T; 7:100870414-100870414 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.780G>A; p.T260T; 7:100870414-100870414 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1120G>A; p.G374S; 7:100871663-100871663 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1235_1237delAGG; p.E414delE; 7:100872680-100872682 |
large_intestine | carcinoma; adenocarcinoma | Deletion - In frame |
c.708A>C; p.R236S; 7:100868839-100868839 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.833A>G; p.Q278R; 7:100870577-100870577 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.254delG; p.G87fs*11; 7:100868124-100868124 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.254delG; p.G87fs*11; 7:100868124-100868124 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.254delG; p.G87fs*11; 7:100868124-100868124 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.254delG; p.G87fs*11; 7:100868124-100868124 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.254delG; p.G87fs*11; 7:100868124-100868124 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.254delG; p.G87fs*11; 7:100868124-100868124 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.254delG; p.G87fs*11; 7:100868124-100868124 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.739C>T; p.P247S; 7:100870373-100870373 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.543C>T; p.C181C; 7:100868674-100868674 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.114C>G; p.L38L; 7:100867865-100867865 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.422C>T; p.A141V; 7:100868553-100868553 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1350G>A; p.P450P; 7:100873222-100873222 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.918A>G; p.V306V; 7:100870662-100870662 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1054C>T; p.R352W; 7:100871597-100871597 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1325A>G; p.E442G; 7:100873197-100873197 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1325A>G; p.E442G; 7:100873197-100873197 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.688G>A; p.V230I; 7:100868819-100868819 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.917_918delTA; p.C307fs*82; 7:100870661-100870662 |
liver | carcinoma | Deletion - Frameshift |
c.1263G>T; p.L421L; 7:100872708-100872708 |
liver | carcinoma | Substitution - coding silent |
c.1263G>T; p.L421L; 7:100872708-100872708 |
liver | carcinoma | Substitution - coding silent |
c.925A>C; p.T309P; 7:100870669-100870669 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1265A>G; p.D422G; 7:100872710-100872710 |
liver | carcinoma | Substitution - Missense |
c.1265A>G; p.D422G; 7:100872710-100872710 |
liver | carcinoma | Substitution - Missense |
c.1002C>A; p.A334A; 7:100871545-100871545 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1322C>G; p.S441C; 7:100873194-100873194 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.853G>T; p.D285Y; 7:100870597-100870597 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.579G>T; p.G193G; 7:100868710-100868710 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1414G>A; p.V472I; 7:100873286-100873286 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.505C>A; p.P169T; 7:100868636-100868636 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.790G>T; p.V264F; 7:100870424-100870424 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1054C>T; p.R352W; 7:100871597-100871597 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1023G>C; p.T341T; 7:100871566-100871566 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.859G>T; p.V287F; 7:100870603-100870603 |
oesophagus | carcinoma | Substitution - Missense |
c.569A>G; p.Q190R; 7:100868700-100868700 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1206C>T; p.C402C; 7:100872651-100872651 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1250G>T; p.R417I; 7:100872695-100872695 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.892C>T; p.R298C; 7:100870636-100870636 |
skin | malignant_melanoma | Substitution - Missense |
c.1126C>T; p.P376S; 7:100871669-100871669 |
skin | malignant_melanoma | Substitution - Missense |
c.943C>T; p.R315C; 7:100870687-100870687 |
skin | malignant_melanoma | Substitution - Missense |
c.733C>T; p.Q245*; 7:100868864-100868864 |
skin | malignant_melanoma | Substitution - Nonsense |
c.619G>A; p.E207K; 7:100868750-100868750 |
skin | malignant_melanoma | Substitution - Missense |
c.886C>T; p.L296F; 7:100870630-100870630 |
skin | malignant_melanoma | Substitution - Missense |
c.604C>T; p.L202F; 7:100868735-100868735 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1319C>T; p.S440F; 7:100873191-100873191 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.892C>T; p.R298C; 7:100870636-100870636 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1079C>A; p.P360H; 7:100871622-100871622 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1085G>C; p.C362S; 7:100871628-100871628 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.963C>A; p.A321A; 7:100870707-100870707 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.925A>G; p.T309A; 7:100870669-100870669 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1108C>T; p.R370C; 7:100871651-100871651 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1284C>T; p.G428G; 7:100872729-100872729 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1073A>G; p.Y358C; 7:100871616-100871616 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.688G>A; p.V230I; 7:100868819-100868819 |
thyroid | other; neoplasm | Substitution - Missense |
c.1087T>C; p.F363L; 7:100871630-100871630 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1116C>T; p.L372L; 7:100871659-100871659 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.926C>G; p.T309R; 7:100870670-100870670 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.926C>G; p.T309R; 7:100870670-100870670 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.943C>T; p.R315C; 7:100870687-100870687 |
urinary_tract; bladder | carcinoma | Substitution - Missense |