| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 10393 |
Name | ANAPC10 |
Synonymous | anaphase promoting complex subunit 10;ANAPC10;anaphase promoting complex subunit 10 |
Definition | anaphase-promoting complex subunit 10|cyclosome subunit 10 |
Position | 4q31 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.68G>A; p.R23Q; 4:145096032-145096032 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.542A>T; p.Y181F; 4:144995389-144995389 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.220G>A; p.V74M; 4:145064679-145064679 |
breast | carcinoma | Substitution - Missense |
c.534C>A; p.F178L; 4:144995397-144995397 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.545G>A; p.R182H; 4:144995386-144995386 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.76G>T; p.G26W; 4:145096024-145096024 |
skin | malignant_melanoma | Substitution - Missense |
c.307C>T; p.H103Y; 4:145064592-145064592 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.459G>A; p.M153I; 4:144995472-144995472 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.398G>A; p.R133H; 4:144995533-144995533 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.396T>C; p.T132T; 4:144995535-144995535 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.6T>G; p.T2T; 4:145096094-145096094 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.254C>T; p.S85F; 4:145064645-145064645 |
skin | malignant_melanoma | Substitution - Missense |
c.511C>A; p.P171T; 4:144995420-144995420 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.454C>G; p.H152D; 4:144995477-144995477 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.198C>T; p.I66I; 4:145081668-145081668 |
liver | carcinoma | Substitution - coding silent |
c.198C>T; p.I66I; 4:145081668-145081668 |
liver | carcinoma | Substitution - coding silent |
c.384T>C; p.H128H; 4:144995547-144995547 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.442G>A; p.G148R; 4:144995489-144995489 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.67C>T; p.R23W; 4:145096033-145096033 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.147T>C; p.N49N; 4:145081719-145081719 |
liver | carcinoma | Substitution - coding silent |
c.147T>C; p.N49N; 4:145081719-145081719 |
liver | carcinoma | Substitution - coding silent |
c.309C>T; p.H103H; 4:145064590-145064590 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.267T>C; p.Y89Y; 4:145064632-145064632 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.544C>T; p.R182C; 4:144995387-144995387 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1A>G; p.M1V; 4:145096099-145096099 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.136C>T; p.R46*; 4:145081730-145081730 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |