| 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 [3 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_021032 | FGF12 | chr3:g.192309240G>C |
| NM_004113 | FGF12 | chr3:g.192449191G>A |
| NM_004113 | FGF12 | chr3:g.192476270G>A |
| Somatic mutations that alter predicted mRNA-miRNA target sites [46 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_004113 | FGF12 | chr3:g.192143939T>A |
| NM_021032 | FGF12 | chr3:g.192143939T>A |
| NM_004113 | FGF12 | chr3:g.192142030C>T |
| NM_021032 | FGF12 | chr3:g.192142030C>T |
| NM_004113 | FGF12 | chr3:g.192140645C>T |
| NM_021032 | FGF12 | chr3:g.192140645C>T |
| NM_004113 | FGF12 | chr3:g.192141063G>A |
| NM_021032 | FGF12 | chr3:g.192141063G>A |
| NM_004113 | FGF12 | chr3:g.192141935A>G |
| NM_021032 | FGF12 | chr3:g.192141935A>G |
| NM_004113 | FGF12 | chr3:g.192143887T>A |
| NM_021032 | FGF12 | chr3:g.192143887T>A |
| NM_004113 | FGF12 | chr3:g.192143991C>A |
| NM_021032 | FGF12 | chr3:g.192143991C>A |
| NM_004113 | FGF12 | chr3:g.192143484T>G |
| NM_021032 | FGF12 | chr3:g.192143484T>G |
| NM_004113 | FGF12 | chr3:g.192143460T>C |
| NM_021032 | FGF12 | chr3:g.192143460T>C |
| NM_004113 | FGF12 | chr3:g.192143888G>T |
| NM_021032 | FGF12 | chr3:g.192143888G>T |
| NM_004113 | FGF12 | chr3:g.192141334A>G |
| NM_021032 | FGF12 | chr3:g.192141334A>G |
| NM_004113 | FGF12 | chr3:g.192139609G>C |
| NM_021032 | FGF12 | chr3:g.192139609G>C |
| NM_004113 | FGF12 | chr3:g.192141771C>A |
| NM_021032 | FGF12 | chr3:g.192141771C>A |
| NM_004113 | FGF12 | chr3:g.192140221A>G |
| NM_021032 | FGF12 | chr3:g.192140221A>G |
| NM_004113 | FGF12 | chr3:g.192143720G>A |
| NM_021032 | FGF12 | chr3:g.192143720G>A |
| NM_004113 | FGF12 | chr3:g.192140614C>T |
| NM_021032 | FGF12 | chr3:g.192140614C>T |
| NM_004113 | FGF12 | chr3:g.192142239G>C |
| NM_021032 | FGF12 | chr3:g.192142239G>C |
| NM_004113 | FGF12 | chr3:g.192139731C>T |
| NM_021032 | FGF12 | chr3:g.192139731C>T |
| NM_004113 | FGF12 | chr3:g.192141475G>T |
| NM_021032 | FGF12 | chr3:g.192141475G>T |
| NM_004113 | FGF12 | chr3:g.192140152G>T |
| NM_021032 | FGF12 | chr3:g.192140152G>T |
| NM_004113 | FGF12 | chr3:g.192140055A>C |
| NM_021032 | FGF12 | chr3:g.192140055A>C |
| NM_004113 | FGF12 | chr3:g.192140864T>A |
| NM_021032 | FGF12 | chr3:g.192140864T>A |
| NM_004113 | FGF12 | chr3:g.192143973T>C |
| NM_021032 | FGF12 | chr3:g.192143973T>C |