| 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 [5 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001759 | CCND2 | chr12:g.4301784T>C |
| NM_001759 | CCND2 | chr12:g.4304373T>C |
| NM_001759 | CCND2 | chr12:g.4276108T>G |
| NM_001759 | CCND2 | chr12:g.4276127G>C |
| NM_001759 | CCND2 | chr12:g.4276138C>G |
| Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [58 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| hsa_circ_0025059 | CCND2 | chr12:g.4300039G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4300135T>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4300181G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4300272T>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4300443T>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4300537G>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4301396G>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4301632G>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4301784T>C |
| hsa_circ_0025059 | CCND2 | chr12:g.4303147A>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4303266G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4303453G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4304147G>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4304373T>C |
| hsa_circ_0025059 | CCND2 | chr12:g.4304549C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4304774C>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4304793C>G |
| hsa_circ_0025059 | CCND2 | chr12:g.4305136A>G |
| hsa_circ_0025057 | CCND2 | chr12:g.4276025C>A |
| hsa_circ_0025057 | CCND2 | chr12:g.4276037C>T |
| hsa_circ_0025057 | CCND2 | chr12:g.4276053A>C |
| hsa_circ_0025057 | CCND2 | chr12:g.4276085G>A |
| hsa_circ_0025057 | CCND2 | chr12:g.4276088T>G |
| hsa_circ_0025057 | CCND2 | chr12:g.4276090C>T |
| hsa_circ_0025057 | CCND2 | chr12:g.4276108T>G |
| hsa_circ_0025057 | CCND2 | chr12:g.4276127G>C |
| hsa_circ_0025057 | CCND2 | chr12:g.4276138C>G |
| hsa_circ_0025057 | CCND2 | chr12:g.4276180G>A |
| hsa_circ_0025057 | CCND2 | chr12:g.4276202C>A |
| hsa_circ_0025057 | CCND2 | chr12:g.4276202C>G |
| hsa_circ_0025059 | CCND2 | chr12:g.4278820G>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4278904G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4278905C>G |
| hsa_circ_0025059 | CCND2 | chr12:g.4278907C>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4278917C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4288846T>C |
| hsa_circ_0025059 | CCND2 | chr12:g.4288854C>G |
| hsa_circ_0025059 | CCND2 | chr12:g.4288854C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4288855C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4288863C>G |
| hsa_circ_0025059 | CCND2 | chr12:g.4288869C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4288870G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4288876C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4288877G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4288896C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4299922C>G |
| hsa_circ_0025059 | CCND2 | chr12:g.4299923C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4299923C>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4299924G>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4299928G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4299932C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4299940C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4299941G>C |
| hsa_circ_0025059 | CCND2 | chr12:g.4299941G>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4299942G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4299956G>A |
| hsa_circ_0025059 | CCND2 | chr12:g.4300000C>T |
| hsa_circ_0025059 | CCND2 | chr12:g.4300007T>C |
| Somatic mutations that alter predicted mRNA-miRNA target sites [19 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001759 | CCND2 | chr12:g.4304373T>C |
| NM_001759 | CCND2 | chr12:g.4300272T>A |
| NM_001759 | CCND2 | chr12:g.4301396G>T |
| NM_001759 | CCND2 | chr12:g.4303266G>A |
| NM_001759 | CCND2 | chr12:g.4304147G>T |
| NM_001759 | CCND2 | chr12:g.4304793C>G |
| NM_001759 | CCND2 | chr12:g.4304774C>A |
| NM_001759 | CCND2 | chr12:g.4300537G>T |
| NM_001759 | CCND2 | chr12:g.4300181G>A |
| NM_001759 | CCND2 | chr12:g.4302676T>G |
| NM_001759 | CCND2 | chr12:g.4304549C>T |
| NM_001759 | CCND2 | chr12:g.4301632G>T |
| NM_001759 | CCND2 | chr12:g.4300443T>A |
| NM_001759 | CCND2 | chr12:g.4301784T>C |
| NM_001759 | CCND2 | chr12:g.4303147A>T |
| NM_001759 | CCND2 | chr12:g.4304664C>A |
| NM_001759 | CCND2 | chr12:g.4300135T>A |
| NM_001759 | CCND2 | chr12:g.4305136A>G |
| NM_001759 | CCND2 | chr12:g.4303453G>A |