| 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 [28 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001101669 | INPP4B | chr4:g.142035451T>A |
| NM_001101669 | INPP4B | chr4:g.142055088C>G |
| hsa_circ_0071029 | INPP4B | chr4:g.142287952C>A |
| hsa_circ_0071035 | INPP4B | chr4:g.142465515A>C |
| NM_001101669 | INPP4B | chr4:g.142563098C>T |
| NM_001101669 | INPP4B | chr4:g.142028831C>A |
| NM_001101669 | INPP4B | chr4:g.142028839G>T |
| NM_001101669 | INPP4B | chr4:g.142028861C>T |
| hsa_circ_0071028 | INPP4B | chr4:g.142123329G>T |
| hsa_circ_0071028 | INPP4B | chr4:g.142123337A>T |
| hsa_circ_0071028 | INPP4B | chr4:g.142123345A>T |
| hsa_circ_0071028 | INPP4B | chr4:g.142123349C>G |
| hsa_circ_0071032 | INPP4B | chr4:g.142160525G>A |
| hsa_circ_0071032 | INPP4B | chr4:g.142160526T>G |
| hsa_circ_0071032 | INPP4B | chr4:g.142160527T>C |
| hsa_circ_0071032 | INPP4B | chr4:g.142160535G>A |
| hsa_circ_0071032 | INPP4B | chr4:g.142160545A>T |
| hsa_circ_0071032 | INPP4B | chr4:g.142260499G>A |
| hsa_circ_0071032 | INPP4B | chr4:g.142260509T>C |
| hsa_circ_0071032 | INPP4B | chr4:g.142260516G>C |
| hsa_circ_0071032 | INPP4B | chr4:g.142260520A>C |
| hsa_circ_0071032 | INPP4B | chr4:g.142260522G>A |
| hsa_circ_0071032 | INPP4B | chr4:g.142260523C>A |
| hsa_circ_0071032 | INPP4B | chr4:g.142260530G>T |
| hsa_circ_0071032 | INPP4B | chr4:g.142260537C>T |
| hsa_circ_0071032 | INPP4B | chr4:g.142260537C>A |
| hsa_circ_0071032 | INPP4B | chr4:g.142260539C>A |
| hsa_circ_0071035 | INPP4B | chr4:g.142305468C>T |
| Somatic mutations that alter predicted mRNA-miRNA target sites [18 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001101669 | INPP4B | chr4:g.142028508T>C |
| NM_003866 | INPP4B | chr4:g.142028508T>C |
| NM_001101669 | INPP4B | chr4:g.142028546G>A |
| NM_003866 | INPP4B | chr4:g.142028546G>A |
| NM_003866 | INPP4B | chr4:g.142028494G>C |
| NM_001101669 | INPP4B | chr4:g.142028494G>C |
| NM_003866 | INPP4B | chr4:g.142028233A>G |
| NM_001101669 | INPP4B | chr4:g.142028233A>G |
| NM_003866 | INPP4B | chr4:g.142028617G>A |
| NM_001101669 | INPP4B | chr4:g.142028617G>A |
| NM_003866 | INPP4B | chr4:g.142028255G>A |
| NM_001101669 | INPP4B | chr4:g.142028255G>A |
| NM_003866 | INPP4B | chr4:g.142028596A>T |
| NM_001101669 | INPP4B | chr4:g.142028596A>T |
| NM_003866 | INPP4B | chr4:g.142028528T>G |
| NM_001101669 | INPP4B | chr4:g.142028528T>G |
| NM_003866 | INPP4B | chr4:g.142028173G>T |
| NM_001101669 | INPP4B | chr4:g.142028173G>T |