| 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 [10 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001114978 | TP63 | chr3:g.189678749C>T |
| NM_001114978 | TP63 | chr3:g.189869355G>A |
| NM_001114978 | TP63 | chr3:g.189869357C>T |
| NM_001114978 | TP63 | chr3:g.189869360C>T |
| hsa_circ_0068516 | TP63 | chr3:g.189890849C>A |
| hsa_circ_0068516 | TP63 | chr3:g.189890849C>T |
| hsa_circ_0068516 | TP63 | chr3:g.189890859C>T |
| hsa_circ_0068516 | TP63 | chr3:g.189890865G>C |
| hsa_circ_0068516 | TP63 | chr3:g.189890876C>T |
| hsa_circ_0068516 | TP63 | chr3:g.189890879G>A |
| Somatic mutations that alter predicted mRNA-miRNA target sites [36 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001114978 | TP63 | chr3:g.189894246C>T |
| NM_001114981 | TP63 | chr3:g.189894246C>T |
| NM_001114981 | TP63 | chr3:g.189896847C>T |
| NM_001114978 | TP63 | chr3:g.189894247G>A |
| NM_001114981 | TP63 | chr3:g.189894247G>A |
| NM_001114979 | TP63 | chr3:g.189880247A>G |
| NM_001114982 | TP63 | chr3:g.189880247A>G |
| NM_001114978 | TP63 | chr3:g.189896847C>T |
| NM_001114980 | TP63 | chr3:g.189896847C>T |
| NM_003722 | TP63 | chr3:g.189896847C>T |
| NM_001114978 | TP63 | chr3:g.189894239C>T |
| NM_001114981 | TP63 | chr3:g.189894239C>T |
| NM_001114978 | TP63 | chr3:g.189894368C>T |
| NM_001114981 | TP63 | chr3:g.189894368C>T |
| NM_001114979 | TP63 | chr3:g.189881130A>G |
| NM_001114982 | TP63 | chr3:g.189881130A>G |
| NM_001114978 | TP63 | chr3:g.189894498A>G |
| NM_001114981 | TP63 | chr3:g.189894498A>G |
| NM_001114981 | TP63 | chr3:g.189896203C>T |
| NM_001114980 | TP63 | chr3:g.189896203C>T |
| NM_003722 | TP63 | chr3:g.189896203C>T |
| NM_001114978 | TP63 | chr3:g.189896203C>T |
| NM_001114979 | TP63 | chr3:g.189880257G>A |
| NM_001114982 | TP63 | chr3:g.189880257G>A |
| NM_001114981 | TP63 | chr3:g.189897094A>G |
| NM_001114980 | TP63 | chr3:g.189897094A>G |
| NM_003722 | TP63 | chr3:g.189897094A>G |
| NM_001114978 | TP63 | chr3:g.189897094A>G |
| NM_001114981 | TP63 | chr3:g.189896146C>T |
| NM_001114980 | TP63 | chr3:g.189896146C>T |
| NM_003722 | TP63 | chr3:g.189896146C>T |
| NM_001114978 | TP63 | chr3:g.189896146C>T |
| NM_001114981 | TP63 | chr3:g.189894871G>A |
| NM_001114980 | TP63 | chr3:g.189894871G>A |
| NM_003722 | TP63 | chr3:g.189894871G>A |
| NM_001114978 | TP63 | chr3:g.189894871G>A |