| SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions |
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| Browse genes associated with cancer risk that contain miRNA related somatic mutations |
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| Somatic mutations that alter miRNA target sites: CLASH [8 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_015335 | MED13L | chr12:g.115986398G>A |
| NM_015335 | MED13L | chr12:g.115986399C>T |
| NM_015335 | MED13L | chr12:g.115986405C>T |
| NM_015335 | MED13L | chr12:g.115986412C>T |
| NM_015335 | MED13L | chr12:g.115991493A>T |
| NM_015335 | MED13L | chr12:g.115991525G>A |
| NM_015335 | MED13L | chr12:g.115991526C>T |
| NM_015335 | MED13L | chr12:g.115991528G>A |
| Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [83 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| hsa_circ_0028549 | MED13L | chr12:g.115960775C>T |
| hsa_circ_0028549 | MED13L | chr12:g.115961089T>C |
| hsa_circ_0028585 | MED13L | chr12:g.116084980A>G |
| hsa_circ_0028549 | MED13L | chr12:g.115961330C>T |
| hsa_circ_0028549 | MED13L | chr12:g.115961350G>A |
| hsa_circ_0028549 | MED13L | chr12:g.115961350G>T |
| hsa_circ_0028549 | MED13L | chr12:g.115961360C>T |
| hsa_circ_0028555 | MED13L | chr12:g.115969027C>T |
| hsa_circ_0028555 | MED13L | chr12:g.115969030G>A |
| hsa_circ_0028555 | MED13L | chr12:g.115970629A>T |
| hsa_circ_0028555 | MED13L | chr12:g.115970653C>T |
| hsa_circ_0028559 | MED13L | chr12:g.115975284A>C |
| hsa_circ_0028563 | MED13L | chr12:g.115975540G>A |
| hsa_circ_0028563 | MED13L | chr12:g.115975549G>C |
| hsa_circ_0028564 | MED13L | chr12:g.115980793T>C |
| hsa_circ_0028564 | MED13L | chr12:g.115980799C>T |
| hsa_circ_0028564 | MED13L | chr12:g.115980806T>C |
| hsa_circ_0028564 | MED13L | chr12:g.115980854G>A |
| hsa_circ_0028565 | MED13L | chr12:g.115982483GGAC>C |
| hsa_circ_0028565 | MED13L | chr12:g.115983328T>A |
| hsa_circ_0028565 | MED13L | chr12:g.115983331G>A |
| hsa_circ_0028565 | MED13L | chr12:g.115983498T>C |
| hsa_circ_0028565 | MED13L | chr12:g.115983499A>G |
| hsa_circ_0028568 | MED13L | chr12:g.115984199A>C |
| hsa_circ_0028568 | MED13L | chr12:g.115984203C>T |
| hsa_circ_0028571 | MED13L | chr12:g.115987121C>T |
| hsa_circ_0028571 | MED13L | chr12:g.115987188G>A |
| hsa_circ_0028571 | MED13L | chr12:g.115987191C>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991174T>C |
| hsa_circ_0028571 | MED13L | chr12:g.115991190C>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991197A>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991238C>A |
| hsa_circ_0028571 | MED13L | chr12:g.115991242G>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991254A>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991260C>G |
| hsa_circ_0028571 | MED13L | chr12:g.115991398A>G |
| hsa_circ_0028571 | MED13L | chr12:g.115991422C>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991442A>C |
| hsa_circ_0028571 | MED13L | chr12:g.115991550C>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991565G>A |
| hsa_circ_0028571 | MED13L | chr12:g.115991605G>A |
| hsa_circ_0028571 | MED13L | chr12:g.115991611C>T |
| hsa_circ_0028571 | MED13L | chr12:g.115991611C>G |
| hsa_circ_0028571 | MED13L | chr12:g.115991904A>T |
| hsa_circ_0028573 | MED13L | chr12:g.115996555C>T |
| hsa_circ_0028573 | MED13L | chr12:g.115996563G>A |
| hsa_circ_0028573 | MED13L | chr12:g.115996601G>A |
| hsa_circ_0028573 | MED13L | chr12:g.115996608T>G |
| hsa_circ_0028573 | MED13L | chr12:g.115996674C>A |
| hsa_circ_0028573 | MED13L | chr12:g.115997032G>T |
| hsa_circ_0028573 | MED13L | chr12:g.115997101G>A |
| hsa_circ_0028573 | MED13L | chr12:g.116005919C>T |
| hsa_circ_0028573 | MED13L | chr12:g.116005947T>C |
| hsa_circ_0028573 | MED13L | chr12:g.116005964G>A |
| hsa_circ_0028573 | MED13L | chr12:g.116005968C>T |
| hsa_circ_0028573 | MED13L | chr12:g.116005986G>T |
| hsa_circ_0028573 | MED13L | chr12:g.116006340T>G |
| hsa_circ_0028573 | MED13L | chr12:g.116006346G>A |
| hsa_circ_0028578 | MED13L | chr12:g.116007485G>A |
| hsa_circ_0028578 | MED13L | chr12:g.116007488G>A |
| hsa_circ_0028578 | MED13L | chr12:g.116007546A>G |
| hsa_circ_0028578 | MED13L | chr12:g.116007596G>T |
| hsa_circ_0028578 | MED13L | chr12:g.116008433G>T |
| hsa_circ_0028578 | MED13L | chr12:g.116008610C>T |
| hsa_circ_0028578 | MED13L | chr12:g.116008612C>T |
| hsa_circ_0028578 | MED13L | chr12:g.116008640G>A |
| hsa_circ_0028578 | MED13L | chr12:g.116008822G>A |
| hsa_circ_0028578 | MED13L | chr12:g.116008856G>T |
| hsa_circ_0028578 | MED13L | chr12:g.116008899G>C |
| hsa_circ_0028578 | MED13L | chr12:g.116008920G>T |
| hsa_circ_0028578 | MED13L | chr12:g.116008930G>A |
| hsa_circ_0028578 | MED13L | chr12:g.116009007C>T |
| hsa_circ_0028578 | MED13L | chr12:g.116009015G>A |
| hsa_circ_0028578 | MED13L | chr12:g.116009095C>T |
| hsa_circ_0028579 | MED13L | chr12:g.116015155G>A |
| hsa_circ_0028579 | MED13L | chr12:g.116015156G>TG |
| hsa_circ_0028579 | MED13L | chr12:g.116015163A>G |
| hsa_circ_0028579 | MED13L | chr12:g.116015190C>T |
| hsa_circ_0028582 | MED13L | chr12:g.116019851AG>G |
| hsa_circ_0028582 | MED13L | chr12:g.116019866G>A |
| hsa_circ_0028582 | MED13L | chr12:g.116019869C>T |
| hsa_circ_0028582 | MED13L | chr12:g.116019941G>A |
| hsa_circ_0028582 | MED13L | chr12:g.116019942C>T |
| Somatic mutations that alter predicted mRNA-miRNA target sites [9 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_015335 | MED13L | chr12:g.115960960C>T |
| NM_015335 | MED13L | chr12:g.115960276A>G |
| NM_015335 | MED13L | chr12:g.115960961G>A |
| NM_015335 | MED13L | chr12:g.115959344C>T |
| NM_015335 | MED13L | chr12:g.115960064G>T |
| NM_015335 | MED13L | chr12:g.115960775C>T |
| NM_015335 | MED13L | chr12:g.115960992G>A |
| NM_015335 | MED13L | chr12:g.115961089T>C |
| NM_015335 | MED13L | chr12:g.115960063G>A |