| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 4602 |
Name | MYB |
Synonymous | v-myb avian myeloblastosis viral oncogene homolog;MYB;v-myb avian myeloblastosis viral oncogene homolog |
Definition | c-myb protein (140 AA)|c-myb10A_CDS|c-myb13A_CDS|c-myb14A_CDS|c-myb8B_CDS|proto-oncogene c-Myb|transcriptional activator Myb |
Position | 6q22-q23 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1391C>T; p.P464L; 6:135200129-135200129 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.26_27insA; p.Y10fs*2; 6:135185905-135185906 |
breast | carcinoma | Insertion - Frameshift |
c.441G>A; p.W147*; 6:135190261-135190261 |
breast | carcinoma | Substitution - Nonsense |
c.1212C>G; p.N404K; 6:135198916-135198916 |
breast | carcinoma | Substitution - Missense |
c.916G>A; p.E306K; 6:135194428-135194428 |
breast | carcinoma | Substitution - Missense |
c.290_292delAAG; p.E99delE; 6:135189867-135189869 |
breast | carcinoma | Deletion - In frame |
c.418_419insCA; p.E141fs*81; 6:135190238-135190239 |
breast | carcinoma | Insertion - Frameshift |
c.810_823delCAATGTCCCTCAGC; p.N271fs*10; 6:135193885-135193898 |
breast | carcinoma | Deletion - Frameshift |
c.1207T>G; p.L403V; 6:135198911-135198911 |
breast | carcinoma | Substitution - Missense |
c.308T>C; p.V103A; 6:135190128-135190128 |
breast | carcinoma | Substitution - Missense |
c.403C>T; p.H135Y; 6:135190223-135190223 |
breast | carcinoma | Substitution - Missense |
c.281_282insT; p.W95fs*37; 6:135189858-135189859 |
breast | carcinoma | Insertion - Frameshift |
c.601G>T; p.E201*; 6:135192397-135192397 |
breast | carcinoma | Substitution - Nonsense |
c.850_851delTA; p.Y284fs*1; 6:135194362-135194363 |
breast | carcinoma | Deletion - Frameshift |
c.785C>T; p.P262L; 6:135193860-135193860 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1593A>G; p.E531E; 6:135201644-135201644 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.769A>G; p.S257G; 6:135193844-135193844 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1019G>A; p.G340E; 6:135195818-135195818 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.901C>T; p.L301F; 6:135194413-135194413 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1705C>A; p.L569I; 6:135203223-135203223 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.187T>C; p.W63R; 6:135187879-135187879 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1597C>T; p.P533S; 6:135201648-135201648 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.104_105insAGC; p.K35_R36insA; 6:135185983-135185984 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemia | Insertion - In frame |
c.105G>T; p.K35N; 6:135185984-135185984 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemia | Substitution - Missense |
c.345G>A; p.W115*; 6:135190165-135190165 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Nonsense |
c.244T>C; p.W82R; 6:135189821-135189821 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.214-1G>C; p.?; 6:135189790-135189790 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelofibrosis | Unknown |
c.1595C>T; p.S532F; 6:135201646-135201646 |
kidney | carcinoma; renal_cell_carcinoma | Substitution - Missense |
c.1025G>A; p.S342N; 6:135195824-135195824 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.727G>T; p.D243Y; 6:135192523-135192523 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.340C>T; p.R114C; 6:135190160-135190160 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.572G>A; p.R191Q; 6:135192368-135192368 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1391C>G; p.P464R; 6:135200129-135200129 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1832C>T; p.A611V; 6:135217889-135217889 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.465T>G; p.I155M; 6:135190285-135190285 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.508G>A; p.A170T; 6:135190328-135190328 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1808C>G; p.P603R; 6:135217865-135217865 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.83G>T; p.G28V; 6:135185962-135185962 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1430A>G; p.Q477R; 6:135200168-135200168 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.341G>A; p.R114H; 6:135190161-135190161 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1443C>T; p.Y481Y; 6:135200181-135200181 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.671C>T; p.A224V; 6:135192467-135192467 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.976G>A; p.G326R; 6:135195775-135195775 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.390T>C; p.C130C; 6:135190210-135190210 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.859G>T; p.E287*; 6:135194371-135194371 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1870A>C; p.S624R; 6:135217927-135217927 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.507C>T; p.I169I; 6:135190327-135190327 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.388T>C; p.C130R; 6:135190208-135190208 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.146A>G; p.E49G; 6:135187838-135187838 |
liver | carcinoma | Substitution - Missense |
c.325A>C; p.K109Q; 6:135190145-135190145 |
liver | carcinoma | Substitution - Missense |
c.325A>C; p.K109Q; 6:135190145-135190145 |
liver | carcinoma | Substitution - Missense |
c.1417G>T; p.A473S; 6:135200155-135200155 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.372G>T; p.G124G; 6:135190192-135190192 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.523G>A; p.G175R; 6:135190343-135190343 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1489G>T; p.D497Y; 6:135200317-135200317 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.116G>C; p.G39A; 6:135185995-135185995 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.933A>T; p.G311G; 6:135194445-135194445 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.389G>A; p.C130Y; 6:135190209-135190209 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.184G>A; p.D62N; 6:135187876-135187876 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1473C>T; p.P491P; 6:135200301-135200301 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.238_240delCAC; p.H80delH; 6:135189815-135189817 |
lung | carcinoma; small_cell_carcinoma | Deletion - In frame |
c.549C>G; p.N183K; 6:135192345-135192345 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.671C>T; p.A224V; 6:135192467-135192467 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.128G>T; p.W43L; 6:135186007-135186007 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.285G>T; p.W95C; 6:135189862-135189862 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1027G>T; p.A343S; 6:135195826-135195826 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1741G>C; p.D581H; 6:135203259-135203259 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1817G>C; p.S606T; 6:135217874-135217874 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1828C>A; p.P610T; 6:135217885-135217885 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.428A>C; p.K143T; 6:135190248-135190248 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1910C>T; p.T637M; 6:135217967-135217967 |
oesophagus | carcinoma | Substitution - Missense |
c.1464T>C; p.P488P; 6:135200292-135200292 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1707T>A; p.L569L; 6:135203225-135203225 |
oesophagus | carcinoma | Substitution - coding silent |
c.1000G>A; p.D334N; 6:135195799-135195799 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.1677C>T; p.T559T; 6:135201728-135201728 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1540G>C; p.E514Q; 6:135200368-135200368 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.366A>G; p.L122L; 6:135190186-135190186 |
pancreas | carcinoma | Substitution - coding silent |
c.1906C>A; p.R636R; 6:135217963-135217963 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1670C>T; p.T557M; 6:135201721-135201721 |
prostate | carcinoma | Substitution - Missense |
c.1142C>T; p.T381I; 6:135195941-135195941 |
skin | malignant_melanoma | Substitution - Missense |
c.1142C>T; p.T381I; 6:135195941-135195941 |
skin | malignant_melanoma | Substitution - Missense |
c.734C>T; p.S245F; 6:135192530-135192530 |
skin | malignant_melanoma | Substitution - Missense |
c.1567C>A; p.L523M; 6:135200395-135200395 |
skin | malignant_melanoma | Substitution - Missense |
c.999C>T; p.A333A; 6:135195798-135195798 |
skin | malignant_melanoma | Substitution - coding silent |
c.1161delG; p.N388fs*3; 6:135195960-135195960 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.494G>A; p.R165K; 6:135190314-135190314 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.91C>T; p.P31S; 6:135185970-135185970 |
skin | malignant_melanoma | Substitution - Missense |
c.992C>T; p.T331I; 6:135195791-135195791 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.437C>T; p.S146F; 6:135190257-135190257 |
skin | malignant_melanoma | Substitution - Missense |
c.816C>T; p.V272V; 6:135193891-135193891 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1394G>A; p.R465K; 6:135200132-135200132 |
skin | malignant_melanoma | Substitution - Missense |
c.1716C>T; p.S572S; 6:135203234-135203234 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1561C>T; p.P521S; 6:135200389-135200389 |
skin | malignant_melanoma | Substitution - Missense |
c.1171G>T; p.E391*; 6:135195970-135195970 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.1000G>A; p.D334N; 6:135195799-135195799 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.642C>T; p.F214F; 6:135192438-135192438 |
skin | malignant_melanoma | Substitution - coding silent |
c.888G>A; p.K296K; 6:135194400-135194400 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.53A>C; p.D18A; 6:135185932-135185932 |
skin | malignant_melanoma | Substitution - Missense |
c.1128C>T; p.I376I; 6:135195927-135195927 |
skin | malignant_melanoma | Substitution - coding silent |
c.1128C>T; p.I376I; 6:135195927-135195927 |
skin | malignant_melanoma | Substitution - coding silent |
c.1128C>T; p.I376I; 6:135195927-135195927 |
skin | malignant_melanoma | Substitution - coding silent |
c.632C>T; p.A211V; 6:135192428-135192428 |
skin | malignant_melanoma | Substitution - Missense |
c.1071G>A; p.L357L; 6:135195870-135195870 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1917C>A; p.V639V; 6:135217974-135217974 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.106C>T; p.R36C; 6:135185985-135185985 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.806T>C; p.I269T; 6:135193881-135193881 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1228G>A; p.E410K; 6:135198932-135198932 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1529G>A; p.G510E; 6:135200357-135200357 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.421G>C; p.E141Q; 6:135190241-135190241 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1272C>T; p.L424L; 6:135198976-135198976 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1272C>T; p.L424L; 6:135198976-135198976 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.1868C>T; p.S623F; 6:135217925-135217925 |
urinary_tract; bladder | carcinoma | Substitution - Missense |