| 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 [30 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| hsa_circ_0077525 | LIN28B | chr6:g.105078816G>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105079195T>C |
| hsa_circ_0077525 | LIN28B | chr6:g.105080561C>A |
| hsa_circ_0077525 | LIN28B | chr6:g.104958269G>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105026313G>C |
| hsa_circ_0077525 | LIN28B | chr6:g.105026316G>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105026349G>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105026393G>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105026394G>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105026400G>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078467C>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078476A>G |
| hsa_circ_0077525 | LIN28B | chr6:g.105078477G>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078483C>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078495G>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105078505C>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078517A>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078561G>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078563G>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105078564A>C |
| hsa_circ_0077525 | LIN28B | chr6:g.105078577G>C |
| hsa_circ_0077525 | LIN28B | chr6:g.105078588A>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078594T>C |
| hsa_circ_0077525 | LIN28B | chr6:g.105078596C>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078600T>C |
| hsa_circ_0077525 | LIN28B | chr6:g.105078641C>A |
| hsa_circ_0077525 | LIN28B | chr6:g.105078751G>C |
| hsa_circ_0077525 | LIN28B | chr6:g.105078754C>T |
| hsa_circ_0077525 | LIN28B | chr6:g.105078758C>G |
| hsa_circ_0077525 | LIN28B | chr6:g.105078770G>A |
| Somatic mutations that alter predicted mRNA-miRNA target sites [15 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001004317 | LIN28B | chr6:g.105079195T>C |
| NM_001004317 | LIN28B | chr6:g.105082943G>T |
| NM_001004317 | LIN28B | chr6:g.105080561C>A |
| NM_001004317 | LIN28B | chr6:g.105079874G>A |
| NM_001004317 | LIN28B | chr6:g.105082164T>C |
| NM_001004317 | LIN28B | chr6:g.105082320T>G |
| NM_001004317 | LIN28B | chr6:g.105080448G>T |
| NM_001004317 | LIN28B | chr6:g.105083081T>A |
| NM_001004317 | LIN28B | chr6:g.105078816G>A |
| NM_001004317 | LIN28B | chr6:g.105080182T>C |
| NM_001004317 | LIN28B | chr6:g.105081047T>C |
| NM_001004317 | LIN28B | chr6:g.105082102C>A |
| NM_001004317 | LIN28B | chr6:g.105082460A>G |
| NM_001004317 | LIN28B | chr6:g.105079351C>G |
| NM_001004317 | LIN28B | chr6:g.105083063C>T |