| 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 [58 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001202474 | PGR | chr11:g.101037763C>T |
| NM_001202474 | PGR | chr11:g.101030238T>C |
| NM_000926 | PGR | chr11:g.101037763C>T |
| NM_000926 | PGR | chr11:g.101038557G>T |
| NM_000926 | PGR | chr11:g.101038556A>T |
| NM_001202474 | PGR | chr11:g.101038556A>T |
| NM_000926 | PGR | chr11:g.101030238T>C |
| NM_001202474 | PGR | chr11:g.101038557G>T |
| NM_000926 | PGR | chr11:g.101038352T>C |
| NM_001202474 | PGR | chr11:g.101038352T>C |
| NM_001202474 | PGR | chr11:g.101030742T>C |
| NM_000926 | PGR | chr11:g.101030742T>C |
| NM_001202474 | PGR | chr11:g.101036670A>T |
| NM_000926 | PGR | chr11:g.101036670A>T |
| NM_001202474 | PGR | chr11:g.101032193T>C |
| NM_000926 | PGR | chr11:g.101032193T>C |
| NM_001202474 | PGR | chr11:g.101031844G>A |
| NM_000926 | PGR | chr11:g.101031844G>A |
| NM_001202474 | PGR | chr11:g.101033440A>C |
| NM_000926 | PGR | chr11:g.101033440A>C |
| NM_001202474 | PGR | chr11:g.101031512T>C |
| NM_000926 | PGR | chr11:g.101031512T>C |
| NM_001202474 | PGR | chr11:g.101032716A>C |
| NM_000926 | PGR | chr11:g.101032716A>C |
| NM_001202474 | PGR | chr11:g.101034453A>G |
| NM_000926 | PGR | chr11:g.101034453A>G |
| NM_001202474 | PGR | chr11:g.101037255G>T |
| NM_000926 | PGR | chr11:g.101037255G>T |
| NM_001202474 | PGR | chr11:g.101030778C>T |
| NM_000926 | PGR | chr11:g.101030778C>T |
| NM_001202474 | PGR | chr11:g.101034495T>A |
| NM_000926 | PGR | chr11:g.101034495T>A |
| NM_001202474 | PGR | chr11:g.101034920A>G |
| NM_000926 | PGR | chr11:g.101034920A>G |
| NM_001202474 | PGR | chr11:g.101031564C>A |
| NM_000926 | PGR | chr11:g.101031564C>A |
| NM_001202474 | PGR | chr11:g.101035015G>C |
| NM_000926 | PGR | chr11:g.101035015G>C |
| NM_001202474 | PGR | chr11:g.101035865A>T |
| NM_000926 | PGR | chr11:g.101035865A>T |
| NM_001202474 | PGR | chr11:g.101032480A>T |
| NM_000926 | PGR | chr11:g.101032480A>T |
| NM_001202474 | PGR | chr11:g.101029972T>A |
| NM_000926 | PGR | chr11:g.101029972T>A |
| NM_001202474 | PGR | chr11:g.101036842C>T |
| NM_000926 | PGR | chr11:g.101036842C>T |
| NM_001202474 | PGR | chr11:g.101029836C>T |
| NM_000926 | PGR | chr11:g.101029836C>T |
| NM_001202474 | PGR | chr11:g.101037537G>T |
| NM_000926 | PGR | chr11:g.101037537G>T |
| NM_001202474 | PGR | chr11:g.101037933A>T |
| NM_000926 | PGR | chr11:g.101037933A>T |
| NM_001202474 | PGR | chr11:g.101033558A>T |
| NM_000926 | PGR | chr11:g.101033558A>T |
| NM_001202474 | PGR | chr11:g.101031955G>T |
| NM_000926 | PGR | chr11:g.101031955G>T |
| NM_001202474 | PGR | chr11:g.101030302G>C |
| NM_000926 | PGR | chr11:g.101030302G>C |