| 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 [56 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| hsa_circ_0018167 | PARD3 | chr10:g.34207381G>A |
| hsa_circ_0018167 | PARD3 | chr10:g.34212046A>G |
| hsa_circ_0018171 | PARD3 | chr10:g.34312322A>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34345586G>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34371506A>C |
| hsa_circ_0018183 | PARD3 | chr10:g.34403666A>G |
| hsa_circ_0018183 | PARD3 | chr10:g.34416763T>C |
| hsa_circ_0018183 | PARD3 | chr10:g.34637303G>C |
| hsa_circ_0018183 | PARD3 | chr10:g.34661789C>T |
| hsa_circ_0018183 | PARD3 | chr10:g.34664982C>A |
| hsa_circ_0018183 | PARD3 | chr10:g.34719656A>T |
| hsa_circ_0018183 | PARD3 | chr10:g.34778859C>T |
| hsa_circ_0018167 | PARD3 | chr10:g.34131513G>A |
| hsa_circ_0018167 | PARD3 | chr10:g.34131545G>A |
| hsa_circ_0018167 | PARD3 | chr10:g.34131547G>A |
| hsa_circ_0018171 | PARD3 | chr10:g.34269744C>T |
| hsa_circ_0018171 | PARD3 | chr10:g.34284207C>T |
| hsa_circ_0018171 | PARD3 | chr10:g.34284214G>C |
| hsa_circ_0018171 | PARD3 | chr10:g.34317225G>A |
| hsa_circ_0018171 | PARD3 | chr10:g.34317228AG>G |
| hsa_circ_0018171 | PARD3 | chr10:g.34317282A>G |
| hsa_circ_0018171 | PARD3 | chr10:g.34317304G>A |
| hsa_circ_0018174 | PARD3 | chr10:g.34337311G>A |
| hsa_circ_0018174 | PARD3 | chr10:g.34337311G>C |
| hsa_circ_0018174 | PARD3 | chr10:g.34337312C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34337349G>A |
| hsa_circ_0018174 | PARD3 | chr10:g.34341708C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34341737T>C |
| hsa_circ_0018174 | PARD3 | chr10:g.34359232C>G |
| hsa_circ_0018174 | PARD3 | chr10:g.34360184G>A |
| hsa_circ_0018174 | PARD3 | chr10:g.34360226G>A |
| hsa_circ_0018174 | PARD3 | chr10:g.34378010C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34378013GC>C |
| hsa_circ_0018174 | PARD3 | chr10:g.34378019G>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34378020C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34378022C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34378024C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34382621C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34382628G>A |
| hsa_circ_0018174 | PARD3 | chr10:g.34382656C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34382662A>C |
| hsa_circ_0018174 | PARD3 | chr10:g.34382666G>A |
| hsa_circ_0018174 | PARD3 | chr10:g.34382681A>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34382689C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34382830C>T |
| hsa_circ_0018174 | PARD3 | chr10:g.34382832A>G |
| hsa_circ_0018174 | PARD3 | chr10:g.34382834C>G |
| hsa_circ_0018183 | PARD3 | chr10:g.34401884G>T |
| hsa_circ_0018183 | PARD3 | chr10:g.34401887C>T |
| hsa_circ_0018183 | PARD3 | chr10:g.34470106T>C |
| hsa_circ_0018183 | PARD3 | chr10:g.34470123C>G |
| hsa_circ_0018183 | PARD3 | chr10:g.34470138ACAG>G |
| hsa_circ_0018183 | PARD3 | chr10:g.34470146C>G |
| hsa_circ_0018183 | PARD3 | chr10:g.34517033C>T |
| hsa_circ_0018183 | PARD3 | chr10:g.34696362G>A |
| hsa_circ_0018183 | PARD3 | chr10:g.34696366A>G |
| Somatic mutations that alter predicted mRNA-miRNA target sites [35 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001184785 | PARD3 | chr10:g.34110527C>A |
| NM_001184786 | PARD3 | chr10:g.34110527C>A |
| NM_001184787 | PARD3 | chr10:g.34110527C>A |
| NM_001184788 | PARD3 | chr10:g.34110527C>A |
| NM_001184789 | PARD3 | chr10:g.34110527C>A |
| NM_001184790 | PARD3 | chr10:g.34110527C>A |
| NM_001184791 | PARD3 | chr10:g.34110527C>A |
| NM_019619 | PARD3 | chr10:g.34110527C>A |
| NM_001184790 | PARD3 | chr10:g.34110436G>A |
| NM_001184787 | PARD3 | chr10:g.34110436G>A |
| NM_001184786 | PARD3 | chr10:g.34110436G>A |
| NM_001184788 | PARD3 | chr10:g.34110436G>A |
| NM_001184791 | PARD3 | chr10:g.34110436G>A |
| NM_001184785 | PARD3 | chr10:g.34110436G>A |
| NM_001184789 | PARD3 | chr10:g.34110436G>A |
| NM_019619 | PARD3 | chr10:g.34110436G>A |
| NM_001184790 | PARD3 | chr10:g.34111155G>A |
| NM_001184787 | PARD3 | chr10:g.34111155G>A |
| NM_001184786 | PARD3 | chr10:g.34111155G>A |
| NM_001184788 | PARD3 | chr10:g.34111155G>A |
| NM_001184791 | PARD3 | chr10:g.34111155G>A |
| NM_001184785 | PARD3 | chr10:g.34111155G>A |
| NM_001184789 | PARD3 | chr10:g.34111155G>A |
| NM_019619 | PARD3 | chr10:g.34111155G>A |
| NM_001184794 | PARD3 | chr10:g.34312322A>T |
| NM_001184792 | PARD3 | chr10:g.34312322A>T |
| NM_001184793 | PARD3 | chr10:g.34312322A>T |
| NM_001184790 | PARD3 | chr10:g.34110369A>G |
| NM_001184787 | PARD3 | chr10:g.34110369A>G |
| NM_001184786 | PARD3 | chr10:g.34110369A>G |
| NM_001184788 | PARD3 | chr10:g.34110369A>G |
| NM_001184791 | PARD3 | chr10:g.34110369A>G |
| NM_001184785 | PARD3 | chr10:g.34110369A>G |
| NM_001184789 | PARD3 | chr10:g.34110369A>G |
| NM_019619 | PARD3 | chr10:g.34110369A>G |