| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 55272 | ||
Name | IMP3 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.386C>T; p.A129V; 15:75639783-75639783 |
skin | malignant_melanoma | Substitution - Missense |
c.130G>T; p.D44Y; 15:75640039-75640039 |
liver | carcinoma | Substitution - Missense |
c.27G>A; p.E9E; 15:75640142-75640142 |
ovary | other; neoplasm | Substitution - coding silent |
c.521A>G; p.N174S; 15:75639648-75639648 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.68T>C; p.V23A; 15:75640101-75640101 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.227C>T; p.S76L; 15:75639942-75639942 |
breast | carcinoma | Substitution - Missense |
c.249G>A; p.L83L; 15:75639920-75639920 |
pancreas | carcinoma | Substitution - coding silent |
c.97G>A; p.V33M; 15:75640072-75640072 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.415G>C; p.G139R; 15:75639754-75639754 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.517T>C; p.Y173H; 15:75639652-75639652 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.385G>A; p.A129T; 15:75639784-75639784 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.530G>C; p.R177P; 15:75639639-75639639 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.540C>A; p.F180L; 15:75639629-75639629 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.528G>A; p.E176E; 15:75639641-75639641 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.484G>A; p.D162N; 15:75639685-75639685 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.484G>A; p.D162N; 15:75639685-75639685 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.54C>T; p.F18F; 15:75640115-75640115 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.433G>C; p.D145H; 15:75639736-75639736 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.381C>A; p.A127A; 15:75639788-75639788 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.381C>A; p.A127A; 15:75639788-75639788 |
thyroid | other; neoplasm | Substitution - coding silent |
c.381C>A; p.A127A; 15:75639788-75639788 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.545T>C; p.L182P; 15:75639624-75639624 |
skin | malignant_melanoma | Substitution - Missense |
c.334C>T; p.P112S; 15:75639835-75639835 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |