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 [24 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001093772 | KIT | chr4:g.54725966A>G |
NM_001093772 | KIT | chr4:g.54725968T>C |
NM_001093772 | KIT | chr4:g.54725969G>A |
NM_001093772 | KIT | chr4:g.54725970G>A |
NM_001093772 | KIT | chr4:g.54725974G>A |
NM_001093772 | KIT | chr4:g.54725975G>A |
NM_001093772 | KIT | chr4:g.54725976T>C |
NM_001093772 | KIT | chr4:g.54725978G>A |
NM_001093772 | KIT | chr4:g.54725978G>T |
NM_001093772 | KIT | chr4:g.54725979A>G |
NM_001093772 | KIT | chr4:g.54725980A>T |
NM_001093772 | KIT | chr4:g.54725991A>G |
NM_001093772 | KIT | chr4:g.54725993A>G |
NM_001093772 | KIT | chr4:g.54725994A>T |
NM_001093772 | KIT | chr4:g.54725994A>G |
NM_001093772 | KIT | chr4:g.54725995C>A |
NM_001093772 | KIT | chr4:g.54725996G>A |
NM_001093772 | KIT | chr4:g.54725997A>T |
NM_001093772 | KIT | chr4:g.54725997A>G |
NM_001093772 | KIT | chr4:g.54726000T>C |
NM_001093772 | KIT | chr4:g.54726001G>A |
NM_001093772 | KIT | chr4:g.54726003G>A |
NM_001093772 | KIT | chr4:g.54726005A>C |
NM_001093772 | KIT | chr4:g.54726007G>A |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [43 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001093772 | KIT | chr4:g.54738722C>T |
NM_001093772 | KIT | chr4:g.54738754T>C |
NM_001093772 | KIT | chr4:g.54739408G>T |
NM_001093772 | KIT | chr4:g.54739412G>T |
NM_001093772 | KIT | chr4:g.54739641A>G |
NM_001093772 | KIT | chr4:g.54740391A>G |
hsa_circ_0069767 | KIT | chr4:g.54725909CCA>CAC |
hsa_circ_0069767 | KIT | chr4:g.54725913C>T |
hsa_circ_0069767 | KIT | chr4:g.54725914G>A |
hsa_circ_0069767 | KIT | chr4:g.54725915T>C |
hsa_circ_0069767 | KIT | chr4:g.54725916T>C |
hsa_circ_0069766 | KIT | chr4:g.54727848C>T |
hsa_circ_0069766 | KIT | chr4:g.54727856T>A |
hsa_circ_0069766 | KIT | chr4:g.54729419C>T |
hsa_circ_0069766 | KIT | chr4:g.54729420A>G |
hsa_circ_0069766 | KIT | chr4:g.54729427G>T |
hsa_circ_0069766 | KIT | chr4:g.54729427G>A |
hsa_circ_0069766 | KIT | chr4:g.54729428A>G |
hsa_circ_0069766 | KIT | chr4:g.54729429A>G |
hsa_circ_0069766 | KIT | chr4:g.54729432TC>T |
hsa_circ_0069766 | KIT | chr4:g.54729433C>G |
hsa_circ_0069766 | KIT | chr4:g.54729433C>T |
hsa_circ_0069766 | KIT | chr4:g.54729434A>G |
hsa_circ_0069766 | KIT | chr4:g.54729435T>C |
hsa_circ_0069766 | KIT | chr4:g.54729438A>G |
hsa_circ_0069766 | KIT | chr4:g.54729442G>T |
hsa_circ_0069766 | KIT | chr4:g.54729446C>A |
hsa_circ_0069766 | KIT | chr4:g.54729453T>C |
hsa_circ_0069766 | KIT | chr4:g.54729455A>C |
hsa_circ_0069766 | KIT | chr4:g.54731879A>G |
hsa_circ_0069766 | KIT | chr4:g.54731880T>C |
hsa_circ_0069766 | KIT | chr4:g.54731897C>T |
hsa_circ_0069766 | KIT | chr4:g.54736555T>C |
hsa_circ_0069766 | KIT | chr4:g.54736558G>T |
hsa_circ_0069766 | KIT | chr4:g.54736567G>A |
hsa_circ_0069766 | KIT | chr4:g.54736571G>A |
hsa_circ_0069766 | KIT | chr4:g.54736573T>C |
hsa_circ_0069766 | KIT | chr4:g.54737187G>A |
hsa_circ_0069766 | KIT | chr4:g.54737188A>G |
hsa_circ_0069766 | KIT | chr4:g.54737206G>T |
hsa_circ_0069766 | KIT | chr4:g.54737207A>G |
hsa_circ_0069766 | KIT | chr4:g.54737208T>C |
hsa_circ_0069766 | KIT | chr4:g.54737210C>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [26 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_000222 | KIT | chr4:g.54739212C>A |
NM_001093772 | KIT | chr4:g.54739212C>A |
NM_001093772 | KIT | chr4:g.54739641A>G |
NM_000222 | KIT | chr4:g.54739641A>G |
NM_001093772 | KIT | chr4:g.54738793G>A |
NM_000222 | KIT | chr4:g.54738793G>A |
NM_001093772 | KIT | chr4:g.54740391A>G |
NM_000222 | KIT | chr4:g.54740391A>G |
NM_001093772 | KIT | chr4:g.54738754T>C |
NM_000222 | KIT | chr4:g.54738754T>C |
NM_001093772 | KIT | chr4:g.54740088C>A |
NM_000222 | KIT | chr4:g.54740088C>A |
NM_001093772 | KIT | chr4:g.54738722C>T |
NM_000222 | KIT | chr4:g.54738722C>T |
NM_001093772 | KIT | chr4:g.54739442T>G |
NM_000222 | KIT | chr4:g.54739442T>G |
NM_001093772 | KIT | chr4:g.54739468C>A |
NM_000222 | KIT | chr4:g.54739468C>A |
NM_001093772 | KIT | chr4:g.54739408G>T |
NM_000222 | KIT | chr4:g.54739408G>T |
NM_001093772 | KIT | chr4:g.54740257G>T |
NM_000222 | KIT | chr4:g.54740257G>T |
NM_001093772 | KIT | chr4:g.54739819G>C |
NM_000222 | KIT | chr4:g.54739819G>C |
NM_001093772 | KIT | chr4:g.54740256G>T |
NM_000222 | KIT | chr4:g.54740256G>T |