| 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 [30 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001306210 | TGFBR1 | chr9:g.99149565A>G |
| NM_001306210 | TGFBR1 | chr9:g.99150657T>A |
| NM_001306210 | TGFBR1 | chr9:g.99153419C>T |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99128986T>G |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99128987T>C |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99128996G>A |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99128998G>C |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99129004C>T |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99129014G>A |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99129030A>C |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99129059G>A |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99129075C>A |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99129077A>G |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99132739G>T |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99142551C>G |
| hsa_circ_0087731 | TGFBR1 | chr9:g.99142574T>G |
| NM_001306210 | TGFBR1 | chr9:g.99144755G>C |
| NM_001306210 | TGFBR1 | chr9:g.99144755G>A |
| NM_001306210 | TGFBR1 | chr9:g.99144756A>T |
| NM_001306210 | TGFBR1 | chr9:g.99147726A>T |
| NM_001306210 | TGFBR1 | chr9:g.99147728GTTGT>G |
| NM_001306210 | TGFBR1 | chr9:g.99147729T>G |
| NM_001306210 | TGFBR1 | chr9:g.99147738A>G |
| NM_001306210 | TGFBR1 | chr9:g.99147745G>T |
| NM_001306210 | TGFBR1 | chr9:g.99147747T>G |
| NM_001306210 | TGFBR1 | chr9:g.99147760C>T |
| NM_001306210 | TGFBR1 | chr9:g.99147777G>T |
| NM_001306210 | TGFBR1 | chr9:g.99149238G>T |
| NM_001306210 | TGFBR1 | chr9:g.99149252C>T |
| NM_001306210 | TGFBR1 | chr9:g.99149253G>A |
| Somatic mutations that alter predicted mRNA-miRNA target sites [12 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001130916 | TGFBR1 | chr9:g.99151396T>G |
| NM_004612 | TGFBR1 | chr9:g.99151396T>G |
| NM_001130916 | TGFBR1 | chr9:g.99149734C>T |
| NM_004612 | TGFBR1 | chr9:g.99149734C>T |
| NM_001130916 | TGFBR1 | chr9:g.99150734A>C |
| NM_004612 | TGFBR1 | chr9:g.99150734A>C |
| NM_001130916 | TGFBR1 | chr9:g.99150657T>A |
| NM_004612 | TGFBR1 | chr9:g.99150657T>A |
| NM_001130916 | TGFBR1 | chr9:g.99149565A>G |
| NM_004612 | TGFBR1 | chr9:g.99149565A>G |
| NM_001130916 | TGFBR1 | chr9:g.99153419C>T |
| NM_004612 | TGFBR1 | chr9:g.99153419C>T |