| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 51434 |
Name | ANAPC7 |
Synonymous | anaphase promoting complex subunit 7;ANAPC7;anaphase promoting complex subunit 7 |
Definition | anaphase-promoting complex subunit 7|cyclosome subunit 7 |
Position | 12q24.11 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.467C>T; p.T156I; 12:110388565-110388565 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.232A>G; p.K78E; 12:110396322-110396322 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1294G>A; p.D432N; 12:110377456-110377456 |
skin | malignant_melanoma | Substitution - Missense |
c.1332T>G; p.A444A; 12:110377418-110377418 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.246G>T; p.V82V; 12:110396308-110396308 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1061G>T; p.R354I; 12:110381823-110381823 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1460C>T; p.A487V; 12:110376114-110376114 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.718T>A; p.L240M; 12:110386426-110386426 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.663C>T; p.I221I; 12:110387750-110387750 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1566G>A; p.E522E; 12:110374276-110374276 |
thyroid | carcinoma | Substitution - coding silent |
c.1566G>A; p.E522E; 12:110374276-110374276 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.847C>T; p.R283*; 12:110382931-110382931 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1193A>G; p.N398S; 12:110377557-110377557 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1555G>A; p.E519K; 12:110374287-110374287 |
skin | malignant_melanoma | Substitution - Missense |
c.1168C>T; p.R390*; 12:110377582-110377582 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1012A>G; p.S338G; 12:110381872-110381872 |
skin | malignant_melanoma | Substitution - Missense |
c.1561G>A; p.E521K; 12:110374281-110374281 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1012A>G; p.S338G; 12:110381872-110381872 |
skin | malignant_melanoma | Substitution - Missense |
c.1505T>C; p.L502P; 12:110376069-110376069 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.627T>C; p.Y209Y; 12:110387786-110387786 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1289T>A; p.L430*; 12:110377461-110377461 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Nonsense |
c.1561G>T; p.E521*; 12:110374281-110374281 |
pancreas | carcinoma; acinar_carcinoma | Substitution - Nonsense |
c.1141G>A; p.E381K; 12:110377609-110377609 |
breast | carcinoma | Substitution - Missense |
c.155C>T; p.S52F; 12:110396399-110396399 |
breast | carcinoma | Substitution - Missense |
c.1195G>A; p.V399I; 12:110377555-110377555 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.256A>C; p.T86P; 12:110396298-110396298 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.285T>G; p.S95R; 12:110396269-110396269 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1458A>G; p.V486V; 12:110376116-110376116 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.623C>T; p.A208V; 12:110387790-110387790 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.348delA; p.K116fs*22; 12:110395161-110395161 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.328G>A; p.E110K; 12:110395181-110395181 |
breast | carcinoma | Substitution - Missense |
c.1273G>T; p.E425*; 12:110377477-110377477 |
prostate | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.264T>A; p.N88K; 12:110396290-110396290 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.838C>T; p.L280L; 12:110382940-110382940 |
skin | malignant_melanoma | Substitution - coding silent |
c.613T>A; p.W205R; 12:110387800-110387800 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.455G>A; p.R152H; 12:110388577-110388577 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.101+1G>T; p.?; 12:110403526-110403526 |
large_intestine; rectum | carcinoma; adenocarcinoma | Unknown |
c.1104C>T; p.L368L; 12:110381780-110381780 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1087C>T; p.R363W; 12:110381797-110381797 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1087C>T; p.R363W; 12:110381797-110381797 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.817+6T>C; p.?; 12:110386321-110386321 |
liver | carcinoma | Unknown |
c.817+6T>C; p.?; 12:110386321-110386321 |
liver | carcinoma | Unknown |
c.550G>C; p.E184Q; 12:110387863-110387863 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1564G>A; p.E522K; 12:110374278-110374278 |
breast | carcinoma | Substitution - Missense |
c.1581C>T; p.A527A; 12:110374261-110374261 |
skin | malignant_melanoma | Substitution - coding silent |
c.1618G>T; p.G540W; 12:110374224-110374224 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1344_1345insA; p.A449fs*5; 12:110377405-110377406 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1002G>A; p.L334L; 12:110381882-110381882 |
breast | carcinoma | Substitution - coding silent |
c.1086T>C; p.F362F; 12:110381798-110381798 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.611T>G; p.V204G; 12:110387802-110387802 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1408G>A; p.A470T; 12:110376166-110376166 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1695G>A; p.Q565Q; 12:110374147-110374147 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.885C>T; p.C295C; 12:110382893-110382893 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.882A>G; p.G294G; 12:110382896-110382896 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.967C>T; p.R323W; 12:110381917-110381917 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.802C>T; p.L268F; 12:110386342-110386342 |
skin | malignant_melanoma | Substitution - Missense |
c.802C>T; p.L268F; 12:110386342-110386342 |
skin | malignant_melanoma | Substitution - Missense |
c.580C>T; p.Q194*; 12:110387833-110387833 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Nonsense |
c.1655C>T; p.A552V; 12:110374187-110374187 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1612G>A; p.G538R; 12:110374230-110374230 |
liver | carcinoma | Substitution - Missense |
c.1603G>A; p.D535N; 12:110374239-110374239 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.686A>T; p.K229I; 12:110386458-110386458 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.862G>C; p.E288Q; 12:110382916-110382916 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.1245C>T; p.T415T; 12:110377505-110377505 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.862G>C; p.E288Q; 12:110382916-110382916 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.923G>T; p.W308L; 12:110382855-110382855 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1246G>A; p.V416I; 12:110377504-110377504 |
breast | carcinoma | Substitution - Missense |
c.1246G>A; p.V416I; 12:110377504-110377504 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.259G>A; p.G87R; 12:110396295-110396295 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.626A>G; p.Y209C; 12:110387787-110387787 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.872A>C; p.E291A; 12:110382906-110382906 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1395G>A; p.L465L; 12:110376179-110376179 |
breast | carcinoma | Substitution - coding silent |
c.771C>G; p.V257V; 12:110386373-110386373 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.795G>A; p.M265I; 12:110386349-110386349 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.892T>A; p.F298I; 12:110382886-110382886 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1606A>T; p.M536L; 12:110374236-110374236 |
skin | malignant_melanoma | Substitution - Missense |
c.715C>G; p.L239V; 12:110386429-110386429 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.517C>G; p.L173V; 12:110388515-110388515 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1697G>C; p.*566S; 12:110374145-110374145 |
parathyroid | carcinoma | Nonstop extension |