| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 891 |
Name | CCNB1 |
Synonymous | cyclin B1;CCNB1;cyclin B1 |
Definition | G2/mitotic-specific cyclin B1|G2/mitotic-specific cyclin-B1 |
Position | 5q12 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.822C>T; p.D274D; 5:69174993-69174993 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.893G>T; p.G298V; 5:69175064-69175064 |
breast | carcinoma | Substitution - Missense |
c.893G>T; p.G298V; 5:69175064-69175064 |
breast | carcinoma | Substitution - Missense |
c.22-1G>A; p.?; 5:69167907-69167907 |
breast | carcinoma | Unknown |
c.388A>G; p.M130V; 5:69171294-69171294 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.864G>T; p.K288N; 5:69175035-69175035 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.920G>A; p.R307Q; 5:69175091-69175091 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.862A>C; p.K288Q; 5:69175033-69175033 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.344_345delTT; p.S116fs*2; 5:69168324-69168325 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.245C>A; p.P82H; 5:69168225-69168225 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1077T>C; p.G359G; 5:69175531-69175531 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.590T>C; p.V197A; 5:69174294-69174294 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.583C>T; p.R195W; 5:69174287-69174287 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2T>C; p.M1T; 5:69167264-69167264 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.36T>G; p.N12K; 5:69167922-69167922 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.865A>G; p.I289V; 5:69175036-69175036 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.584G>A; p.R195Q; 5:69174288-69174288 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.481G>A; p.G161R; 5:69171387-69171387 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.481G>A; p.G161R; 5:69171387-69171387 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1045T>G; p.F349V; 5:69175499-69175499 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1099C>T; p.H367Y; 5:69177254-69177254 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.449T>C; p.I150T; 5:69171355-69171355 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.131C>T; p.A44V; 5:69168017-69168017 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.703C>T; p.Q235*; 5:69174407-69174407 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.371C>G; p.T124S; 5:69171277-69171277 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.804C>G; p.D268E; 5:69174975-69174975 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.339A>C; p.E113D; 5:69168319-69168319 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.407C>T; p.A136V; 5:69171313-69171313 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.815T>G; p.V272G; 5:69174986-69174986 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.654G>T; p.L218F; 5:69174358-69174358 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.210T>G; p.A70A; 5:69168190-69168190 |
liver | carcinoma | Substitution - coding silent |
c.210T>G; p.A70A; 5:69168190-69168190 |
liver | carcinoma | Substitution - coding silent |
c.407C>A; p.A136D; 5:69171313-69171313 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.588A>C; p.E196D; 5:69174292-69174292 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1084-1G>C; p.?; 5:69177238-69177238 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.579G>C; p.L193L; 5:69174283-69174283 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1200C>T; p.V400V; 5:69177529-69177529 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1027C>G; p.Q343E; 5:69175481-69175481 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1027C>G; p.Q343E; 5:69175481-69175481 |
lung | carcinoma; bronchioloalveolar_adenocarcinoma | Substitution - Missense |
c.679G>C; p.V227L; 5:69174383-69174383 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1237A>T; p.S413C; 5:69177566-69177566 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.804C>G; p.D268E; 5:69174975-69174975 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.922A>T; p.R308*; 5:69175093-69175093 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.950T>C; p.V317A; 5:69175404-69175404 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.885T>C; p.F295F; 5:69175056-69175056 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.915_916CC>TT; p.L306F; 5:69175086-69175087 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.915C>T; p.F305F; 5:69175086-69175086 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1018C>T; p.P340S; 5:69175472-69175472 |
skin; head_neck | malignant_melanoma; superficial_spreading | Substitution - Missense |
c.184A>T; p.M62L; 5:69168070-69168070 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.612C>T; p.I204I; 5:69174316-69174316 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.558A>G; p.A186A; 5:69174262-69174262 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.868C>G; p.L290V; 5:69175039-69175039 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.920G>A; p.R307Q; 5:69175091-69175091 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.665C>T; p.T222I; 5:69174369-69174369 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1302A>G; p.*434*; 5:69177631-69177631 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.966G>A; p.L322L; 5:69175420-69175420 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1267G>C; p.V423L; 5:69177596-69177596 |
urinary_tract; bladder | carcinoma | Substitution - Missense |