| 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_001144918 | FGFR2 | chr10:g.121478893C>T |
| Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [2 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001144918 | FGFR2 | chr10:g.121479183G>T |
| hsa_circ_0020233 | FGFR2 | chr10:g.121498556G>T |
| Somatic mutations that alter predicted mRNA-miRNA target sites [43 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_000141 | FGFR2 | chr10:g.121478674A>T |
| NM_001144914 | FGFR2 | chr10:g.121478674A>T |
| NM_001144915 | FGFR2 | chr10:g.121478674A>T |
| NM_001144916 | FGFR2 | chr10:g.121478674A>T |
| NM_001144917 | FGFR2 | chr10:g.121478674A>T |
| NM_001144918 | FGFR2 | chr10:g.121478674A>T |
| NM_022970 | FGFR2 | chr10:g.121478674A>T |
| NM_000141 | FGFR2 | chr10:g.121479598C>T |
| NM_001144914 | FGFR2 | chr10:g.121479598C>T |
| NM_001144916 | FGFR2 | chr10:g.121479598C>T |
| NM_001144917 | FGFR2 | chr10:g.121479598C>T |
| NM_001144918 | FGFR2 | chr10:g.121479598C>T |
| NM_022970 | FGFR2 | chr10:g.121479598C>T |
| NM_001144913 | FGFR2 | chr10:g.121482015G>A |
| NM_001144919 | FGFR2 | chr10:g.121482015G>A |
| NM_001144916 | FGFR2 | chr10:g.121478481G>A |
| NM_001144915 | FGFR2 | chr10:g.121478481G>A |
| NM_001144914 | FGFR2 | chr10:g.121478481G>A |
| NM_000141 | FGFR2 | chr10:g.121478481G>A |
| NM_022970 | FGFR2 | chr10:g.121478481G>A |
| NM_001144918 | FGFR2 | chr10:g.121478481G>A |
| NM_001144917 | FGFR2 | chr10:g.121478481G>A |
| NM_001144915 | FGFR2 | chr10:g.121479183G>T |
| NM_001144914 | FGFR2 | chr10:g.121479183G>T |
| NM_000141 | FGFR2 | chr10:g.121479183G>T |
| NM_022970 | FGFR2 | chr10:g.121479183G>T |
| NM_001144918 | FGFR2 | chr10:g.121479183G>T |
| NM_001144917 | FGFR2 | chr10:g.121479183G>T |
| NM_001144916 | FGFR2 | chr10:g.121479183G>T |
| NM_001144916 | FGFR2 | chr10:g.121478893C>T |
| NM_001144915 | FGFR2 | chr10:g.121478893C>T |
| NM_001144914 | FGFR2 | chr10:g.121478893C>T |
| NM_000141 | FGFR2 | chr10:g.121478893C>T |
| NM_022970 | FGFR2 | chr10:g.121478893C>T |
| NM_001144918 | FGFR2 | chr10:g.121478893C>T |
| NM_001144917 | FGFR2 | chr10:g.121478893C>T |
| NM_001144916 | FGFR2 | chr10:g.121479070G>T |
| NM_001144915 | FGFR2 | chr10:g.121479070G>T |
| NM_001144914 | FGFR2 | chr10:g.121479070G>T |
| NM_000141 | FGFR2 | chr10:g.121479070G>T |
| NM_022970 | FGFR2 | chr10:g.121479070G>T |
| NM_001144918 | FGFR2 | chr10:g.121479070G>T |
| NM_001144917 | FGFR2 | chr10:g.121479070G>T |