| 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 [68 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NR_046000 | IRF4 | chr6:g.407806G>A |
| NR_046000 | IRF4 | chr6:g.408206G>A |
| NR_046000 | IRF4 | chr6:g.408445C>T |
| NR_046000 | IRF4 | chr6:g.408577G>C |
| NR_046000 | IRF4 | chr6:g.408962A>G |
| NR_046000 | IRF4 | chr6:g.409013C>G |
| NR_046000 | IRF4 | chr6:g.409318G>C |
| NR_046000 | IRF4 | chr6:g.409602T>C |
| NR_046000 | IRF4 | chr6:g.410024A>C |
| NR_046000 | IRF4 | chr6:g.410514T>C |
| NR_046000 | IRF4 | chr6:g.410727C>T |
| hsa_circ_0001570 | IRF4 | chr6:g.411331A>T |
| hsa_circ_0001569 | IRF4 | chr6:g.393157A>G |
| hsa_circ_0001569 | IRF4 | chr6:g.393178G>A |
| hsa_circ_0001569 | IRF4 | chr6:g.393188C>T |
| hsa_circ_0001569 | IRF4 | chr6:g.393199C>T |
| hsa_circ_0001569 | IRF4 | chr6:g.393203G>A |
| hsa_circ_0001569 | IRF4 | chr6:g.393204A>G |
| hsa_circ_0001569 | IRF4 | chr6:g.393205G>A |
| hsa_circ_0001569 | IRF4 | chr6:g.393205G>C |
| hsa_circ_0001569 | IRF4 | chr6:g.393206C>G |
| hsa_circ_0001569 | IRF4 | chr6:g.393206C>T |
| hsa_circ_0001569 | IRF4 | chr6:g.393222C>T |
| hsa_circ_0001569 | IRF4 | chr6:g.393246A>G |
| hsa_circ_0001569 | IRF4 | chr6:g.393249G>A |
| hsa_circ_0001569 | IRF4 | chr6:g.393251C>G |
| hsa_circ_0001569 | IRF4 | chr6:g.393267G>A |
| hsa_circ_0001569 | IRF4 | chr6:g.393270C>G |
| hsa_circ_0001569 | IRF4 | chr6:g.393294A>C |
| hsa_circ_0001569 | IRF4 | chr6:g.393296C>A |
| hsa_circ_0075415 | IRF4 | chr6:g.395890C>T |
| hsa_circ_0075415 | IRF4 | chr6:g.395911G>A |
| hsa_circ_0075415 | IRF4 | chr6:g.395920T>G |
| hsa_circ_0075416 | IRF4 | chr6:g.397130C>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397138G>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397142G>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397147T>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397158C>T |
| hsa_circ_0075416 | IRF4 | chr6:g.397159G>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397159G>T |
| hsa_circ_0075416 | IRF4 | chr6:g.397164G>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397170G>T |
| hsa_circ_0075416 | IRF4 | chr6:g.397188G>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397206G>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397217G>A |
| hsa_circ_0075416 | IRF4 | chr6:g.397219G>A |
| hsa_circ_0075415 | IRF4 | chr6:g.401436A>C |
| hsa_circ_0075415 | IRF4 | chr6:g.401457A>C |
| hsa_circ_0075415 | IRF4 | chr6:g.401482G>A |
| hsa_circ_0075415 | IRF4 | chr6:g.401485C>T |
| hsa_circ_0075415 | IRF4 | chr6:g.401488C>T |
| hsa_circ_0075415 | IRF4 | chr6:g.401490C>T |
| hsa_circ_0075415 | IRF4 | chr6:g.401494G>A |
| hsa_circ_0075415 | IRF4 | chr6:g.401501C>T |
| hsa_circ_0075415 | IRF4 | chr6:g.401513G>T |
| hsa_circ_0075415 | IRF4 | chr6:g.401555C>T |
| hsa_circ_0075415 | IRF4 | chr6:g.401567G>A |
| hsa_circ_0075415 | IRF4 | chr6:g.401567G>T |
| hsa_circ_0075415 | IRF4 | chr6:g.401593G>C |
| hsa_circ_0075415 | IRF4 | chr6:g.401609C>A |
| hsa_circ_0075415 | IRF4 | chr6:g.401626C>G |
| hsa_circ_0075415 | IRF4 | chr6:g.401636G>C |
| NR_046000 | IRF4 | chr6:g.407524T>C |
| NR_046000 | IRF4 | chr6:g.407544C>T |
| NR_046000 | IRF4 | chr6:g.407546G>A |
| NR_046000 | IRF4 | chr6:g.407567G>A |
| NR_046000 | IRF4 | chr6:g.407568A>G |
| NR_046000 | IRF4 | chr6:g.407593G>T |
| Somatic mutations that alter predicted mRNA-miRNA target sites [28 records found] |
| [download data table] |
| Transcript ID | Gene Symbol | Mutation ID |
|---|---|---|
| NM_001195286 | IRF4 | chr6:g.410514T>C |
| NM_002460 | IRF4 | chr6:g.410514T>C |
| NM_001195286 | IRF4 | chr6:g.407806G>A |
| NM_002460 | IRF4 | chr6:g.407806G>A |
| NM_001195286 | IRF4 | chr6:g.411331A>T |
| NM_002460 | IRF4 | chr6:g.411331A>T |
| NM_001195286 | IRF4 | chr6:g.409602T>C |
| NM_002460 | IRF4 | chr6:g.409602T>C |
| NM_001195286 | IRF4 | chr6:g.408577G>C |
| NM_002460 | IRF4 | chr6:g.408577G>C |
| NM_001195286 | IRF4 | chr6:g.410727C>T |
| NM_002460 | IRF4 | chr6:g.410727C>T |
| NM_001195286 | IRF4 | chr6:g.408962A>G |
| NM_002460 | IRF4 | chr6:g.408962A>G |
| NM_001195286 | IRF4 | chr6:g.409013C>G |
| NM_002460 | IRF4 | chr6:g.409013C>G |
| NM_001195286 | IRF4 | chr6:g.408206G>A |
| NM_002460 | IRF4 | chr6:g.408206G>A |
| NM_001195286 | IRF4 | chr6:g.407904C>A |
| NM_002460 | IRF4 | chr6:g.407904C>A |
| NM_001195286 | IRF4 | chr6:g.409318G>C |
| NM_002460 | IRF4 | chr6:g.409318G>C |
| NM_001195286 | IRF4 | chr6:g.408445C>T |
| NM_002460 | IRF4 | chr6:g.408445C>T |
| NM_001195286 | IRF4 | chr6:g.410024A>C |
| NM_002460 | IRF4 | chr6:g.410024A>C |
| NM_001195286 | IRF4 | chr6:g.410998T>G |
| NM_002460 | IRF4 | chr6:g.410998T>G |