| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 1488 |
Name | CTBP2 |
Synonymous | C-terminal binding protein 2;CTBP2;C-terminal binding protein 2 |
Definition | C-terminal-binding protein 2|ribeye |
Position | 10q26.13 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.595G>T; p.G199W; 10:125027165-125027165 |
biliary_tract; bile_duct | carcinoma; adenocarcinoma | Substitution - Missense |
c.227A>G; p.Y76C; 10:125027533-125027533 |
bone; humerus | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1254A>G; p.A418A; 10:125026506-125026506 |
breast | carcinoma | Substitution - coding silent |
c.2280C>T; p.S760S; 10:124994589-124994589 |
breast | carcinoma | Substitution - coding silent |
c.1668A>C; p.A556A; 10:125026092-125026092 |
breast | carcinoma | Substitution - coding silent |
c.1567A>C; p.T523P; 10:125026193-125026193 |
breast | carcinoma | Substitution - Missense |
c.2367C>G; p.N789K; 10:124994502-124994502 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.2468A>T; p.Q823L; 10:124993918-124993918 |
breast | carcinoma | Substitution - Missense |
c.2439C>T; p.G813G; 10:124993947-124993947 |
breast | carcinoma | Substitution - coding silent |
c.2775C>T; p.Y925Y; 10:124992697-124992697 |
breast | carcinoma | Substitution - coding silent |
c.2558C>G; p.A853G; 10:124993303-124993303 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.2626G>A; p.A876T; 10:124993235-124993235 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1950C>G; p.N650K; 10:125002988-125002988 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.2824G>T; p.A942S; 10:124989652-124989652 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.2256_2257ins76; p.L753fs*62; 10:124994612-124994613 |
central_nervous_system; brainstem | glioma; astrocytoma_Grade_IV | Insertion - Frameshift |
c.1276G>A; p.V426M; 10:125026484-125026484 |
central_nervous_system; brain | glioma; oligodendroglioma_Grade_III | Substitution - Missense |
c.2531G>81; p.Q847fs*31; 10:124993855-124993855 |
central_nervous_system; brainstem | glioma; astrocytoma_Grade_II | Unknown |
c.2201C>A; p.A734E; 10:124994668-124994668 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1849G>A; p.V617M; 10:125003089-125003089 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1849G>A; p.V617M; 10:125003089-125003089 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.2049C>T; p.L683L; 10:124998100-124998100 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2783C>A; p.P928Q; 10:124989693-124989693 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2212C>T; p.R738*; 10:124994657-124994657 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.483C>T; p.A161A; 10:125027277-125027277 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.547G>A; p.A183T; 10:125027213-125027213 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1276G>A; p.V426M; 10:125026484-125026484 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2280C>A; p.S760S; 10:124994589-124994589 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2328C>T; p.S776S; 10:124994541-124994541 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2271C>T; p.I757I; 10:124994598-124994598 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.276C>T; p.Y92Y; 10:125027484-125027484 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.836C>A; p.T279N; 10:125026924-125026924 |
haematopoietic_and_lymphoid_tissue; abdomen | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.2099C>A; p.T700K; 10:124998050-124998050 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.2099C>A; p.T700K; 10:124998050-124998050 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.451A>G; p.M151V; 10:125027309-125027309 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.2933A>G; p.N978S; 10:124989543-124989543 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.2882C>T; p.A961V; 10:124989594-124989594 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.700G>A; p.V234M; 10:125027060-125027060 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.2213G>T; p.R738L; 10:124994656-124994656 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.1615C>G; p.Q539E; 10:125026145-125026145 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.559G>A; p.G187R; 10:125027201-125027201 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.2897C>G; p.A966G; 10:124989579-124989579 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.2897C>G; p.A966G; 10:124989579-124989579 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.2917A>T; p.T973S; 10:124989559-124989559 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.464C>T; p.S155L; 10:125027296-125027296 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.2089C>T; p.R697W; 10:124998060-124998060 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.2089C>T; p.R697W; 10:124998060-124998060 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.1615C>T; p.Q539*; 10:125026145-125026145 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Nonsense |
c.206A>G; p.Y69C; 10:125027554-125027554 |
kidney | other; neoplasm | Substitution - Missense |
c.2512C>A; p.H838N; 10:124993874-124993874 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1551A>T; p.A517A; 10:125026209-125026209 |
kidney | other; neoplasm | Substitution - coding silent |
c.2287G>A; p.V763M; 10:124994582-124994582 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1446G>A; p.T482T; 10:125026314-125026314 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.460C>T; p.R154W; 10:125027300-125027300 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1363T>C; p.Y455H; 10:125026397-125026397 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1363T>C; p.Y455H; 10:125026397-125026397 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2629G>T; p.A877S; 10:124993232-124993232 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1215T>C; p.R405R; 10:125026545-125026545 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.529C>T; p.R177W; 10:125027231-125027231 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2251C>T; p.P751S; 10:124994618-124994618 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1129G>A; p.E377K; 10:125026631-125026631 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2452G>A; p.E818K; 10:124993934-124993934 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1902G>T; p.K634N; 10:125003036-125003036 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1902G>T; p.K634N; 10:125003036-125003036 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.418G>A; p.G140R; 10:125027342-125027342 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.418G>A; p.G140R; 10:125027342-125027342 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2099C>A; p.T700K; 10:124998050-124998050 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2090G>A; p.R697Q; 10:124998059-124998059 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.772G>A; p.G258R; 10:125026988-125026988 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.739G>T; p.G247W; 10:125027021-125027021 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.739G>T; p.G247W; 10:125027021-125027021 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.739G>T; p.G247W; 10:125027021-125027021 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1085delG; p.G362fs*86; 10:125026675-125026675 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1045T>A; p.C349S; 10:125026715-125026715 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1085delG; p.G362fs*86; 10:125026675-125026675 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2149C>T; p.R717C; 10:124998000-124998000 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1805C>T; p.A602V; 10:125003366-125003366 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.226T>C; p.Y76H; 10:125027534-125027534 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.536C>T; p.T179I; 10:125027224-125027224 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2212C>T; p.R738*; 10:124994657-124994657 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1609C>T; p.P537S; 10:125026151-125026151 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.399C>T; p.S133S; 10:125027361-125027361 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2562G>A; p.P854P; 10:124993299-124993299 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.893G>A; p.R298Q; 10:125026867-125026867 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1538G>A; p.R513Q; 10:125026222-125026222 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1089G>A; p.P363P; 10:125026671-125026671 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1864T>A; p.Y622N; 10:125003074-125003074 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1864T>A; p.Y622N; 10:125003074-125003074 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.490C>A; p.L164M; 10:125027270-125027270 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1854C>T; p.G618G; 10:125003084-125003084 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1854C>T; p.G618G; 10:125003084-125003084 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.562C>T; p.R188W; 10:125027198-125027198 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1085_1086insG; p.L364fs*19; 10:125026674-125026675 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1085_1086insG; p.L364fs*19; 10:125026674-125026675 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1787C>T; p.T596I; 10:125003384-125003384 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1100C>T; p.A367V; 10:125026660-125026660 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1100C>T; p.A367V; 10:125026660-125026660 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1100C>T; p.A367V; 10:125026660-125026660 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1803C>T; p.D601D; 10:125003368-125003368 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.277G>A; p.D93N; 10:125027483-125027483 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1811C>T; p.S604L; 10:125003360-125003360 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1124G>A; p.R375Q; 10:125026636-125026636 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.775C>T; p.P259S; 10:125026985-125026985 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.775C>T; p.P259S; 10:125026985-125026985 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2201C>T; p.A734V; 10:124994668-124994668 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2498C>T; p.A833V; 10:124993888-124993888 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.125C>T; p.T42M; 10:125027635-125027635 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1175T>C; p.L392P; 10:125026585-125026585 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1615C>G; p.Q539E; 10:125026145-125026145 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1615C>G; p.Q539E; 10:125026145-125026145 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.25A>C; p.N9H; 10:125027735-125027735 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1968C>T; p.A656A; 10:125002970-125002970 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2334C>T; p.C778C; 10:124994535-124994535 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1336G>A; p.A446T; 10:125026424-125026424 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1336G>A; p.A446T; 10:125026424-125026424 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.810C>T; p.Y270Y; 10:125026950-125026950 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1851G>A; p.V617V; 10:125003087-125003087 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1577C>A; p.P526Q; 10:125026183-125026183 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1950C>T; p.N650N; 10:125002988-125002988 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2287G>A; p.V763M; 10:124994582-124994582 |
liver | carcinoma | Substitution - Missense |
c.2287G>A; p.V763M; 10:124994582-124994582 |
liver | carcinoma | Substitution - Missense |
c.2064G>A; p.R688R; 10:124998085-124998085 |
liver | carcinoma | Substitution - coding silent |
c.1821A>G; p.E607E; 10:125003350-125003350 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.2064G>A; p.R688R; 10:124998085-124998085 |
liver | carcinoma | Substitution - coding silent |
c.1746C>T; p.R582R; 10:125003425-125003425 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.1979-8C>T; p.?; 10:124998178-124998178 |
liver | carcinoma | Unknown |
c.2276G>A; p.R759Q; 10:124994593-124994593 |
liver | carcinoma | Substitution - Missense |
c.2213G>C; p.R738P; 10:124994656-124994656 |
liver | carcinoma | Substitution - Missense |
c.528G>T; p.G176G; 10:125027232-125027232 |
liver | carcinoma | Substitution - coding silent |
c.528G>T; p.G176G; 10:125027232-125027232 |
liver | carcinoma | Substitution - coding silent |
c.700G>A; p.V234M; 10:125027060-125027060 |
liver | carcinoma | Substitution - Missense |
c.2601G>T; p.E867D; 10:124993260-124993260 |
liver | carcinoma | Substitution - Missense |
c.1991G>A; p.C664Y; 10:124998158-124998158 |
liver | carcinoma | Substitution - Missense |
c.2288T>C; p.V763A; 10:124994581-124994581 |
liver | carcinoma | Substitution - Missense |
c.1991G>A; p.C664Y; 10:124998158-124998158 |
liver | carcinoma | Substitution - Missense |
c.2799T>C; p.G933G; 10:124989677-124989677 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.724C>T; p.P242S; 10:125027036-125027036 |
liver | carcinoma | Substitution - Missense |
c.1254A>G; p.A418A; 10:125026506-125026506 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2492G>A; p.R831Q; 10:124993894-124993894 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2888C>G; p.P963R; 10:124989588-124989588 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2268G>T; p.G756G; 10:124994601-124994601 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2202G>A; p.A734A; 10:124994667-124994667 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1943A>G; p.Y648C; 10:125002995-125002995 |
meninges | meningioma | Substitution - Missense |
c.410C>T; p.P137L; 10:125027350-125027350 |
NS | malignant_melanoma | Substitution - Missense |
c.410C>T; p.P137L; 10:125027350-125027350 |
NS | malignant_melanoma | Substitution - Missense |
c.2193G>A; p.T731T; 10:124994676-124994676 |
oesophagus | carcinoma | Substitution - coding silent |
c.1169_1170ins21; p.A390_P391insLQPQPAA; 10:125026590-125026591 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Insertion - In frame |
c.2922delA; p.K974fs*>12; 10:124989554-124989554 |
ovary | carcinoma; serous_carcinoma | Deletion - Frameshift |
c.290C>G; p.A97G; 10:125027470-125027470 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1445C>T; p.T482M; 10:125026315-125026315 |
pancreas | carcinoma; acinar_carcinoma | Substitution - Missense |
c.573G>A; p.R191R; 10:125027187-125027187 |
pancreas | carcinoma | Substitution - coding silent |
c.2363A>T; p.H788L; 10:124994506-124994506 |
pancreas | carcinoma; adenocarcinoma | Substitution - Missense |
c.2734G>C; p.D912H; 10:124992738-124992738 |
pancreas | carcinoma | Substitution - Missense |
c.2917A>T; p.T973S; 10:124989559-124989559 |
pancreas | carcinoma | Substitution - Missense |
c.2469A>G; p.Q823Q; 10:124993917-124993917 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.152T>A; p.F51Y; 10:125027608-125027608 |
prostate | carcinoma | Substitution - Missense |
c.2439C>T; p.G813G; 10:124993947-124993947 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2929G>A; p.D977N; 10:124989547-124989547 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1837C>T; p.L613L; 10:125003101-125003101 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1212C>T; p.R404R; 10:125026548-125026548 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2784G>A; p.P928P; 10:124989692-124989692 |
skin | malignant_melanoma | Substitution - coding silent |
c.706C>T; p.P236S; 10:125027054-125027054 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.388C>T; p.P130S; 10:125027372-125027372 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.472C>T; p.L158L; 10:125027288-125027288 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.382C>T; p.R128W; 10:125027378-125027378 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1085delG; p.G362fs*86; 10:125026675-125026675 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.2625G>A; p.E875E; 10:124993236-124993236 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1024C>T; p.L342L; 10:125026736-125026736 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.784G>A; p.E262K; 10:125026976-125026976 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2659G>A; p.G887S; 10:124993202-124993202 |
skin | malignant_melanoma | Substitution - Missense |
c.340C>T; p.P114S; 10:125027420-125027420 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2698G>A; p.E900K; 10:124992774-124992774 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.897G>A; p.A299A; 10:125026863-125026863 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1566C>T; p.S522S; 10:125026194-125026194 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2919delA; p.K974fs*>12; 10:124989557-124989557 |
soft_tissue; striated_muscle | rhabdomyosarcoma | Deletion - Frameshift |
c.2344C>T; p.H782Y; 10:124994525-124994525 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1685G>A; p.R562H; 10:125003486-125003486 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.731G>A; p.G244D; 10:125027029-125027029 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.2284G>T; p.G762C; 10:124994585-124994585 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2451C>T; p.D817D; 10:124993935-124993935 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2255A>G; p.Y752C; 10:124994614-124994614 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.674G>A; p.R225K; 10:125027086-125027086 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |
c.1854C>T; p.G618G; 10:125003084-125003084 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.686C>T; p.P229L; 10:125027074-125027074 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1855G>A; p.A619T; 10:125003083-125003083 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1827C>T; p.H609H; 10:125003344-125003344 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2201C>A; p.A734E; 10:124994668-124994668 |
stomach | carcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable | Substitution - Missense |
c.1835T>C; p.V612A; 10:125003103-125003103 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1806G>A; p.A602A; 10:125003365-125003365 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1363T>C; p.Y455H; 10:125026397-125026397 |
thyroid | other; neoplasm | Substitution - Missense |
c.2351A>G; p.N784S; 10:124994518-124994518 |
thyroid | other; neoplasm | Substitution - Missense |
c.2202G>T; p.A734A; 10:124994667-124994667 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2202G>T; p.A734A; 10:124994667-124994667 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2202G>T; p.A734A; 10:124994667-124994667 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1374G>A; p.Q458Q; 10:125026386-125026386 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2898G>A; p.A966A; 10:124989578-124989578 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2367C>G; p.N789K; 10:124994502-124994502 |
thyroid | other; neoplasm | Substitution - Missense |
c.2933A>G; p.N978S; 10:124989543-124989543 |
thyroid | other; neoplasm | Substitution - Missense |
c.2220G>A; p.K740K; 10:124994649-124994649 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1876A>T; p.T626S; 10:125003062-125003062 |
thyroid | other; neoplasm | Substitution - Missense |
c.2933A>G; p.N978S; 10:124989543-124989543 |
thyroid | other; neoplasm | Substitution - Missense |
c.2363A>T; p.H788L; 10:124994506-124994506 |
thyroid | other; neoplasm | Substitution - Missense |
c.2363A>T; p.H788L; 10:124994506-124994506 |
thyroid | other; neoplasm | Substitution - Missense |
c.2363A>T; p.H788L; 10:124994506-124994506 |
thyroid | other; neoplasm | Substitution - Missense |
c.2363A>T; p.H788L; 10:124994506-124994506 |
thyroid | other; neoplasm | Substitution - Missense |
c.1779C>T; p.D593D; 10:125003392-125003392 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2203G>T; p.V735F; 10:124994666-124994666 |
thyroid | other; neoplasm | Substitution - Missense |
c.2203G>T; p.V735F; 10:124994666-124994666 |
thyroid | other; neoplasm | Substitution - Missense |
c.2203G>T; p.V735F; 10:124994666-124994666 |
thyroid | other; neoplasm | Substitution - Missense |
c.2203G>T; p.V735F; 10:124994666-124994666 |
thyroid | other; neoplasm | Substitution - Missense |
c.2195G>A; p.G732E; 10:124994674-124994674 |
thyroid | other; neoplasm | Substitution - Missense |
c.2195G>A; p.G732E; 10:124994674-124994674 |
thyroid | other; neoplasm | Substitution - Missense |
c.1873A>T; p.I625F; 10:125003065-125003065 |
thyroid | other; neoplasm | Substitution - Missense |
c.2219A>C; p.K740T; 10:124994650-124994650 |
thyroid | other; neoplasm | Substitution - Missense |
c.2219A>C; p.K740T; 10:124994650-124994650 |
thyroid | other; neoplasm | Substitution - Missense |
c.2194G>C; p.G732R; 10:124994675-124994675 |
thyroid | other; neoplasm | Substitution - Missense |
c.2194G>C; p.G732R; 10:124994675-124994675 |
thyroid | other; neoplasm | Substitution - Missense |
c.359T>A; p.V120E; 10:125027401-125027401 |
thyroid | other; neoplasm | Substitution - Missense |
c.1175T>C; p.L392P; 10:125026585-125026585 |
thyroid | other; neoplasm | Substitution - Missense |
c.2248G>T; p.D750Y; 10:124994621-124994621 |
thyroid | other; neoplasm | Substitution - Missense |
c.2241A>G; p.I747M; 10:124994628-124994628 |
thyroid | other; neoplasm | Substitution - Missense |
c.2241A>G; p.I747M; 10:124994628-124994628 |
thyroid | other; neoplasm | Substitution - Missense |
c.2487G>A; p.R829R; 10:124993899-124993899 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2783C>T; p.P928L; 10:124989693-124989693 |
thyroid | other; neoplasm | Substitution - Missense |
c.1761G>C; p.E587D; 10:125003410-125003410 |
thyroid | other; neoplasm | Substitution - Missense |
c.2793C>G; p.I931M; 10:124989683-124989683 |
thyroid | other; neoplasm | Substitution - Missense |
c.2943C>T; p.H981H; 10:124989533-124989533 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2943C>T; p.H981H; 10:124989533-124989533 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1170_1171ins21; p.P391_L392insAAPACGP; 10:125026589-125026590 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1170_1171ins21; p.P391_L392insAAPACGP; 10:125026589-125026590 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1170_1171ins21; p.P391_L392insAAPACGP; 10:125026589-125026590 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1170_1171ins21; p.P391_L392insAAPACGP; 10:125026589-125026590 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1170_1171ins21; p.P391_L392insAAPACGP; 10:125026589-125026590 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.2000C>T; p.P667L; 10:124998149-124998149 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.2000C>T; p.P667L; 10:124998149-124998149 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1347G>A; p.A449A; 10:125026413-125026413 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2868C>A; p.N956K; 10:124989608-124989608 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2868C>A; p.N956K; 10:124989608-124989608 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2868C>A; p.N956K; 10:124989608-124989608 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2868C>A; p.N956K; 10:124989608-124989608 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2868C>A; p.N956K; 10:124989608-124989608 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2868C>A; p.N956K; 10:124989608-124989608 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2367C>G; p.N789K; 10:124994502-124994502 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2363A>T; p.H788L; 10:124994506-124994506 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2335G>A; p.V779I; 10:124994534-124994534 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2286C>T; p.G762G; 10:124994583-124994583 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1615C>G; p.Q539E; 10:125026145-125026145 |
urinary_tract; bladder | carcinoma | Substitution - Missense |