| 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 predicted mRNA-miRNA target sites [57 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_000612 | IGF2 | chr11:g.2131624->CAG |
| NM_001127598 | IGF2 | chr11:g.2131624->CAG |
| NM_001007139 | IGF2 | chr11:g.2131624->CAG |
| NM_000612 | IGF2 | chr11:g.2131629->CAT |
| NM_001127598 | IGF2 | chr11:g.2131629->CAT |
| NM_001007139 | IGF2 | chr11:g.2131629->CAT |
| NM_000612 | IGF2 | chr11:g.2132078T>C |
| NM_001127598 | IGF2 | chr11:g.2132078T>C |
| NM_001007139 | IGF2 | chr11:g.2132078T>C |
| NM_000612 | IGF2 | chr11:g.2130588G>T |
| NM_001127598 | IGF2 | chr11:g.2130588G>T |
| NM_001007139 | IGF2 | chr11:g.2130588G>T |
| NM_000612 | IGF2 | chr11:g.2132075A>G |
| NM_001127598 | IGF2 | chr11:g.2132075A>G |
| NM_001007139 | IGF2 | chr11:g.2132075A>G |
| NM_000612 | IGF2 | chr11:g.2132081G>A |
| NM_001127598 | IGF2 | chr11:g.2132081G>A |
| NM_001007139 | IGF2 | chr11:g.2132081G>A |
| NM_000612 | IGF2 | chr11:g.2130577A>T |
| NM_001127598 | IGF2 | chr11:g.2130577A>T |
| NM_001007139 | IGF2 | chr11:g.2130577A>T |
| NM_000612 | IGF2 | chr11:g.2130606C>T |
| NM_001127598 | IGF2 | chr11:g.2130606C>T |
| NM_001007139 | IGF2 | chr11:g.2130606C>T |
| NM_000612 | IGF2 | chr11:g.2132018G>C |
| NM_001127598 | IGF2 | chr11:g.2132018G>C |
| NM_001007139 | IGF2 | chr11:g.2132018G>C |
| NM_000612 | IGF2 | chr11:g.2130417C>T |
| NM_001127598 | IGF2 | chr11:g.2130417C>T |
| NM_001007139 | IGF2 | chr11:g.2130417C>T |
| NM_000612 | IGF2 | chr11:g.2129540G>A |
| NM_001127598 | IGF2 | chr11:g.2129540G>A |
| NM_001007139 | IGF2 | chr11:g.2129540G>A |
| NM_000612 | IGF2 | chr11:g.2130441G>C |
| NM_001127598 | IGF2 | chr11:g.2130441G>C |
| NM_001007139 | IGF2 | chr11:g.2130441G>C |
| NM_000612 | IGF2 | chr11:g.2129866C>T |
| NM_001127598 | IGF2 | chr11:g.2129866C>T |
| NM_001007139 | IGF2 | chr11:g.2129866C>T |
| NM_000612 | IGF2 | chr11:g.2129357C>T |
| NM_001127598 | IGF2 | chr11:g.2129357C>T |
| NM_001007139 | IGF2 | chr11:g.2129357C>T |
| NM_000612 | IGF2 | chr11:g.2129665G>A |
| NM_001127598 | IGF2 | chr11:g.2129665G>A |
| NM_001007139 | IGF2 | chr11:g.2129665G>A |
| NM_000612 | IGF2 | chr11:g.2129968G>A |
| NM_001127598 | IGF2 | chr11:g.2129968G>A |
| NM_001007139 | IGF2 | chr11:g.2129968G>A |
| NM_000612 | IGF2 | chr11:g.2130494C>T |
| NM_001127598 | IGF2 | chr11:g.2130494C>T |
| NM_001007139 | IGF2 | chr11:g.2130494C>T |
| NM_000612 | IGF2 | chr11:g.2130989G>A |
| NM_001127598 | IGF2 | chr11:g.2130989G>A |
| NM_001007139 | IGF2 | chr11:g.2130989G>A |
| NM_000612 | IGF2 | chr11:g.2129630A>G |
| NM_001127598 | IGF2 | chr11:g.2129630A>G |
| NM_001007139 | IGF2 | chr11:g.2129630A>G |