| 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: PAR-CLIP and HITS-CLIP [3 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_006614 | CHL1 | chr3:g.328289ACC>ATT |
| NM_006614 | CHL1 | chr3:g.394740A>C |
| NM_006614 | CHL1 | chr3:g.394751G>A |
| Somatic mutations that alter predicted mRNA-miRNA target sites [54 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001253387 | CHL1 | chr3:g.406857A>G |
| NM_001253388 | CHL1 | chr3:g.406857A>G |
| NM_006614 | CHL1 | chr3:g.406857A>G |
| NM_001253387 | CHL1 | chr3:g.408012T>C |
| NM_001253388 | CHL1 | chr3:g.408012T>C |
| NM_006614 | CHL1 | chr3:g.408012T>C |
| NM_001253387 | CHL1 | chr3:g.407922T>C |
| NM_001253388 | CHL1 | chr3:g.407922T>C |
| NM_006614 | CHL1 | chr3:g.407922T>C |
| NM_001253388 | CHL1 | chr3:g.409122T>C |
| NM_006614 | CHL1 | chr3:g.409122T>C |
| NM_001253387 | CHL1 | chr3:g.409122T>C |
| NM_001253388 | CHL1 | chr3:g.409059T>G |
| NM_006614 | CHL1 | chr3:g.409059T>G |
| NM_001253387 | CHL1 | chr3:g.409059T>G |
| NM_001253388 | CHL1 | chr3:g.406951C>A |
| NM_006614 | CHL1 | chr3:g.406951C>A |
| NM_001253387 | CHL1 | chr3:g.406951C>A |
| NM_001253388 | CHL1 | chr3:g.407466G>T |
| NM_006614 | CHL1 | chr3:g.407466G>T |
| NM_001253387 | CHL1 | chr3:g.407466G>T |
| NM_001253388 | CHL1 | chr3:g.407748G>T |
| NM_006614 | CHL1 | chr3:g.407748G>T |
| NM_001253387 | CHL1 | chr3:g.407748G>T |
| NM_001253388 | CHL1 | chr3:g.407789T>G |
| NM_006614 | CHL1 | chr3:g.407789T>G |
| NM_001253387 | CHL1 | chr3:g.407789T>G |
| NM_001253388 | CHL1 | chr3:g.407687G>T |
| NM_006614 | CHL1 | chr3:g.407687G>T |
| NM_001253387 | CHL1 | chr3:g.407687G>T |
| NM_001253388 | CHL1 | chr3:g.406285C>T |
| NM_006614 | CHL1 | chr3:g.406285C>T |
| NM_001253387 | CHL1 | chr3:g.406285C>T |
| NM_001253388 | CHL1 | chr3:g.406466C>T |
| NM_006614 | CHL1 | chr3:g.406466C>T |
| NM_001253387 | CHL1 | chr3:g.406466C>T |
| NM_001253388 | CHL1 | chr3:g.407210G>A |
| NM_006614 | CHL1 | chr3:g.407210G>A |
| NM_001253387 | CHL1 | chr3:g.407210G>A |
| NM_001253388 | CHL1 | chr3:g.406280T>C |
| NM_006614 | CHL1 | chr3:g.406280T>C |
| NM_001253387 | CHL1 | chr3:g.406280T>C |
| NM_001253388 | CHL1 | chr3:g.408020T>A |
| NM_006614 | CHL1 | chr3:g.408020T>A |
| NM_001253387 | CHL1 | chr3:g.408020T>A |
| NM_001253388 | CHL1 | chr3:g.409061T>C |
| NM_006614 | CHL1 | chr3:g.409061T>C |
| NM_001253387 | CHL1 | chr3:g.409061T>C |
| NM_001253388 | CHL1 | chr3:g.407093G>A |
| NM_006614 | CHL1 | chr3:g.407093G>A |
| NM_001253387 | CHL1 | chr3:g.407093G>A |
| NM_001253388 | CHL1 | chr3:g.409354A>G |
| NM_006614 | CHL1 | chr3:g.409354A>G |
| NM_001253387 | CHL1 | chr3:g.409354A>G |