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: CLASH [2 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001145098 | SKIL | chr3:g.170361207G>T |
NM_001145098 | SKIL | chr3:g.170361244A>T |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [58 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001145098 | SKIL | chr3:g.170358218C>T |
hsa_circ_0067938 | SKIL | chr3:g.170360288G>A |
NM_001145097 | SKIL | chr3:g.170392456G>GT |
NM_001145097 | SKIL | chr3:g.170393158C>T |
hsa_circ_0067938 | SKIL | chr3:g.170360418GA>G |
hsa_circ_0067938 | SKIL | chr3:g.170360433G>A |
hsa_circ_0067938 | SKIL | chr3:g.170360441A>C |
hsa_circ_0067938 | SKIL | chr3:g.170360468T>C |
hsa_circ_0067938 | SKIL | chr3:g.170360543G>A |
hsa_circ_0067938 | SKIL | chr3:g.170360545A>T |
hsa_circ_0067938 | SKIL | chr3:g.170360582C>T |
hsa_circ_0067938 | SKIL | chr3:g.170360583C>T |
hsa_circ_0067938 | SKIL | chr3:g.170360589G>A |
hsa_circ_0067938 | SKIL | chr3:g.170360605C>G |
hsa_circ_0067938 | SKIL | chr3:g.170360617A>G |
hsa_circ_0067938 | SKIL | chr3:g.170360618G>T |
hsa_circ_0067938 | SKIL | chr3:g.170360631G>T |
hsa_circ_0067938 | SKIL | chr3:g.170360667C>T |
hsa_circ_0067938 | SKIL | chr3:g.170360695C>A |
hsa_circ_0067938 | SKIL | chr3:g.170360713C>G |
hsa_circ_0067938 | SKIL | chr3:g.170360750G>T |
hsa_circ_0067938 | SKIL | chr3:g.170360758G>T |
hsa_circ_0067938 | SKIL | chr3:g.170360795C>T |
hsa_circ_0067938 | SKIL | chr3:g.170360803C>G |
hsa_circ_0067938 | SKIL | chr3:g.170360846A>G |
hsa_circ_0067938 | SKIL | chr3:g.170360972A>G |
hsa_circ_0067938 | SKIL | chr3:g.170360977C>A |
hsa_circ_0067938 | SKIL | chr3:g.170360982C>T |
hsa_circ_0067938 | SKIL | chr3:g.170361103A>G |
hsa_circ_0067938 | SKIL | chr3:g.170361105T>C |
hsa_circ_0067938 | SKIL | chr3:g.170361107G>A |
hsa_circ_0067938 | SKIL | chr3:g.170361108C>T |
hsa_circ_0067938 | SKIL | chr3:g.170361125A>T |
hsa_circ_0067938 | SKIL | chr3:g.170361136C>G |
hsa_circ_0067938 | SKIL | chr3:g.170361273A>T |
hsa_circ_0067938 | SKIL | chr3:g.170361296C>G |
hsa_circ_0067938 | SKIL | chr3:g.170361299C>T |
hsa_circ_0067938 | SKIL | chr3:g.170361314A>G |
hsa_circ_0067938 | SKIL | chr3:g.170361357G>T |
NM_001145097 | SKIL | chr3:g.170381272A>T |
NM_001145097 | SKIL | chr3:g.170381326C>G |
hsa_circ_0008056 | SKIL | chr3:g.170384569A>G |
hsa_circ_0008056 | SKIL | chr3:g.170384573G>A |
hsa_circ_0008056 | SKIL | chr3:g.170384625C>T |
hsa_circ_0067939 | SKIL | chr3:g.170390231A>C |
hsa_circ_0067939 | SKIL | chr3:g.170390242T>C |
hsa_circ_0067939 | SKIL | chr3:g.170390270G>A |
hsa_circ_0067939 | SKIL | chr3:g.170390300A>G |
hsa_circ_0067939 | SKIL | chr3:g.170390318G>A |
hsa_circ_0067939 | SKIL | chr3:g.170390318G>C |
hsa_circ_0067939 | SKIL | chr3:g.170390400G>T |
hsa_circ_0067939 | SKIL | chr3:g.170390404T>C |
NM_001145097 | SKIL | chr3:g.170391164G>C |
NM_001145097 | SKIL | chr3:g.170391168G>T |
NM_001145097 | SKIL | chr3:g.170391184T>A |
NM_001145097 | SKIL | chr3:g.170391200G>A |
NM_001145097 | SKIL | chr3:g.170391203A>G |
NM_001145097 | SKIL | chr3:g.170391210A>G |
Somatic mutations that alter predicted mRNA-miRNA target sites [24 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001145097 | SKIL | chr3:g.170392512G>A |
NM_001145098 | SKIL | chr3:g.170392512G>A |
NM_001248008 | SKIL | chr3:g.170392512G>A |
NM_005414 | SKIL | chr3:g.170392512G>A |
NM_001145097 | SKIL | chr3:g.170393533A>T |
NM_001145098 | SKIL | chr3:g.170393533A>T |
NM_001248008 | SKIL | chr3:g.170393533A>T |
NM_005414 | SKIL | chr3:g.170393533A>T |
NM_001145097 | SKIL | chr3:g.170394830G>T |
NM_001145098 | SKIL | chr3:g.170394830G>T |
NM_001248008 | SKIL | chr3:g.170394830G>T |
NM_005414 | SKIL | chr3:g.170394830G>T |
NM_001145097 | SKIL | chr3:g.170396116C>A |
NM_001145098 | SKIL | chr3:g.170396116C>A |
NM_001248008 | SKIL | chr3:g.170396116C>A |
NM_005414 | SKIL | chr3:g.170396116C>A |
NM_001145097 | SKIL | chr3:g.170393158C>T |
NM_001145098 | SKIL | chr3:g.170393158C>T |
NM_001248008 | SKIL | chr3:g.170393158C>T |
NM_005414 | SKIL | chr3:g.170393158C>T |
NM_001145097 | SKIL | chr3:g.170395192A>T |
NM_001145098 | SKIL | chr3:g.170395192A>T |
NM_001248008 | SKIL | chr3:g.170395192A>T |
NM_005414 | SKIL | chr3:g.170395192A>T |