| 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 [1 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_173647 | RNF149 | chr2:g.101286131C>T |
| Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [25 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| hsa_circ_0055902 | RNF149 | chr2:g.101276960A>G |
| hsa_circ_0055902 | RNF149 | chr2:g.101277246A>T |
| hsa_circ_0055902 | RNF149 | chr2:g.101277254G>T |
| hsa_circ_0055902 | RNF149 | chr2:g.101277263C>G |
| hsa_circ_0055902 | RNF149 | chr2:g.101277274C>T |
| hsa_circ_0055904 | RNF149 | chr2:g.101281899C>A |
| hsa_circ_0055904 | RNF149 | chr2:g.101281899C>T |
| hsa_circ_0055904 | RNF149 | chr2:g.101281908G>A |
| hsa_circ_0055904 | RNF149 | chr2:g.101281936C>A |
| hsa_circ_0055904 | RNF149 | chr2:g.101281971A>T |
| hsa_circ_0055904 | RNF149 | chr2:g.101281984G>A |
| hsa_circ_0055904 | RNF149 | chr2:g.101281994G>C |
| hsa_circ_0055904 | RNF149 | chr2:g.101286102C>T |
| hsa_circ_0055904 | RNF149 | chr2:g.101289024T>C |
| hsa_circ_0055904 | RNF149 | chr2:g.101289044T>C |
| hsa_circ_0055904 | RNF149 | chr2:g.101289056G>C |
| hsa_circ_0055904 | RNF149 | chr2:g.101294050C>T |
| hsa_circ_0055904 | RNF149 | chr2:g.101294050C>A |
| hsa_circ_0055904 | RNF149 | chr2:g.101295076C>A |
| hsa_circ_0055904 | RNF149 | chr2:g.101295089A>G |
| hsa_circ_0055904 | RNF149 | chr2:g.101295097C>G |
| hsa_circ_0055902 | RNF149 | chr2:g.101308208G>T |
| hsa_circ_0055902 | RNF149 | chr2:g.101308394C>T |
| hsa_circ_0055902 | RNF149 | chr2:g.101308497G>C |
| hsa_circ_0055902 | RNF149 | chr2:g.101308497G>T |
| Somatic mutations that alter predicted mRNA-miRNA target sites [2 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_173647 | RNF149 | chr2:g.101276276A>T |
| NM_173647 | RNF149 | chr2:g.101276960A>G |