| 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 [18 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| hsa_circ_0068873 | FGFR3 | chr4:g.1807765C>T |
| hsa_circ_0068869 | FGFR3 | chr4:g.1799410TG>T |
| hsa_circ_0068869 | FGFR3 | chr4:g.1799433C>T |
| hsa_circ_0068873 | FGFR3 | chr4:g.1803747T>C |
| hsa_circ_0068873 | FGFR3 | chr4:g.1803755G>A |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806053C>T |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806055T>A |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806060A>G |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806064A>G |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806068G>A |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806076G>A |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806132C>T |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806135G>A |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806136A>G |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806141C>G |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806142A>G |
| hsa_circ_0068873 | FGFR3 | chr4:g.1806149C>T |
| hsa_circ_0068873 | FGFR3 | chr4:g.1807221CT>CGA |
| Somatic mutations that alter predicted mRNA-miRNA target sites [24 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001163213 | FGFR3 | chr4:g.1807635G>A |
| NM_000142 | FGFR3 | chr4:g.1807635G>A |
| NM_001163213 | FGFR3 | chr4:g.1807921T>C |
| NM_000142 | FGFR3 | chr4:g.1807921T>C |
| NM_022965 | FGFR3 | chr4:g.1807921T>C |
| NM_022965 | FGFR3 | chr4:g.1807635G>A |
| NM_001163213 | FGFR3 | chr4:g.1807404T>C |
| NM_000142 | FGFR3 | chr4:g.1807404T>C |
| NM_022965 | FGFR3 | chr4:g.1807404T>C |
| NM_001163213 | FGFR3 | chr4:g.1807399GC>- |
| NM_000142 | FGFR3 | chr4:g.1807399GC>- |
| NM_022965 | FGFR3 | chr4:g.1807399GC>- |
| NM_001163213 | FGFR3 | chr4:g.1807401GT>- |
| NM_000142 | FGFR3 | chr4:g.1807401GT>- |
| NM_022965 | FGFR3 | chr4:g.1807401GT>- |
| NM_001163213 | FGFR3 | chr4:g.1807412T>G |
| NM_000142 | FGFR3 | chr4:g.1807412T>G |
| NM_022965 | FGFR3 | chr4:g.1807412T>G |
| NM_001163213 | FGFR3 | chr4:g.1807995G>A |
| NM_000142 | FGFR3 | chr4:g.1807995G>A |
| NM_022965 | FGFR3 | chr4:g.1807995G>A |
| NM_001163213 | FGFR3 | chr4:g.1807398T>C |
| NM_000142 | FGFR3 | chr4:g.1807398T>C |
| NM_022965 | FGFR3 | chr4:g.1807398T>C |