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 [54 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_003108 | SOX11 | chr2:g.5694150G>A |
NM_003108 | SOX11 | chr2:g.5694174G>T |
NM_003108 | SOX11 | chr2:g.5694175G>T |
NM_003108 | SOX11 | chr2:g.5694366T>A |
NM_003108 | SOX11 | chr2:g.5694500G>T |
NM_003108 | SOX11 | chr2:g.5694501C>A |
NM_003108 | SOX11 | chr2:g.5695179C>A |
NM_003108 | SOX11 | chr2:g.5695352T>C |
NM_003108 | SOX11 | chr2:g.5692739G>C |
NM_003108 | SOX11 | chr2:g.5692743T>A |
NM_003108 | SOX11 | chr2:g.5692745G>T |
NM_003108 | SOX11 | chr2:g.5692754G>C |
NM_003108 | SOX11 | chr2:g.5692774C>T |
NM_003108 | SOX11 | chr2:g.5692784G>C |
NM_003108 | SOX11 | chr2:g.5693011C>T |
NM_003108 | SOX11 | chr2:g.5693012G>A |
NM_003108 | SOX11 | chr2:g.5693019C>A |
NM_003108 | SOX11 | chr2:g.5693019C>T |
NM_003108 | SOX11 | chr2:g.5693022G>T |
NM_003108 | SOX11 | chr2:g.5693022G>C |
NM_003108 | SOX11 | chr2:g.5693023A>T |
NM_003108 | SOX11 | chr2:g.5693025G>A |
NM_003108 | SOX11 | chr2:g.5693026C>T |
NM_003108 | SOX11 | chr2:g.5693027G>A |
NM_003108 | SOX11 | chr2:g.5693031C>A |
NM_003108 | SOX11 | chr2:g.5693121G>T |
NM_003108 | SOX11 | chr2:g.5693144C>A |
NM_003108 | SOX11 | chr2:g.5693151G>A |
NM_003108 | SOX11 | chr2:g.5693159C>G |
NM_003108 | SOX11 | chr2:g.5693159C>A |
NM_003108 | SOX11 | chr2:g.5693332G>A |
NM_003108 | SOX11 | chr2:g.5693378C>T |
NM_003108 | SOX11 | chr2:g.5693393GGAC>G |
NM_003108 | SOX11 | chr2:g.5693682C>A |
NM_003108 | SOX11 | chr2:g.5693699C>G |
NM_003108 | SOX11 | chr2:g.5693729G>A |
NM_003108 | SOX11 | chr2:g.5693734C>A |
NM_003108 | SOX11 | chr2:g.5693846C>T |
NM_003108 | SOX11 | chr2:g.5693869GC>G |
NM_003108 | SOX11 | chr2:g.5693873C>T |
NM_003108 | SOX11 | chr2:g.5693874G>A |
NM_003108 | SOX11 | chr2:g.5693879G>A |
NM_003108 | SOX11 | chr2:g.5693900G>A |
NM_003108 | SOX11 | chr2:g.5693955G>A |
NM_003108 | SOX11 | chr2:g.5693955G>T |
NM_003108 | SOX11 | chr2:g.5693968A>G |
NM_003108 | SOX11 | chr2:g.5693988G>A |
NM_003108 | SOX11 | chr2:g.5694002G>A |
NM_003108 | SOX11 | chr2:g.5694004A>G |
NM_003108 | SOX11 | chr2:g.5694005C>G |
NM_003108 | SOX11 | chr2:g.5694005C>A |
NM_003108 | SOX11 | chr2:g.5694016C>T |
NM_003108 | SOX11 | chr2:g.5694026C>T |
NM_003108 | SOX11 | chr2:g.5694029C>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [52 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_003108 | SOX11 | chr2:g.5697754T>C |
NM_003108 | SOX11 | chr2:g.5697944T>C |
NM_003108 | SOX11 | chr2:g.5694150G>A |
NM_003108 | SOX11 | chr2:g.5694134A>G |
NM_003108 | SOX11 | chr2:g.5700960C>A |
NM_003108 | SOX11 | chr2:g.5697955C>T |
NM_003108 | SOX11 | chr2:g.5699436A>T |
NM_003108 | SOX11 | chr2:g.5694501C>A |
NM_003108 | SOX11 | chr2:g.5699669->T |
NM_003108 | SOX11 | chr2:g.5697810G>CC |
NM_003108 | SOX11 | chr2:g.5700435G>A |
NM_003108 | SOX11 | chr2:g.5699708G>C |
NM_003108 | SOX11 | chr2:g.5697350C>T |
NM_003108 | SOX11 | chr2:g.5694175G>T |
NM_003108 | SOX11 | chr2:g.5695179C>A |
NM_003108 | SOX11 | chr2:g.5700700G>T |
NM_003108 | SOX11 | chr2:g.5698639G>A |
NM_003108 | SOX11 | chr2:g.5699869G>A |
NM_003108 | SOX11 | chr2:g.5700029G>C |
NM_003108 | SOX11 | chr2:g.5695234G>T |
NM_003108 | SOX11 | chr2:g.5700072G>C |
NM_003108 | SOX11 | chr2:g.5694366T>A |
NM_003108 | SOX11 | chr2:g.5699671T>G |
NM_003108 | SOX11 | chr2:g.5699411T>C |
NM_003108 | SOX11 | chr2:g.5694174G>T |
NM_003108 | SOX11 | chr2:g.5695753T>C |
NM_003108 | SOX11 | chr2:g.5700153G>A |
NM_003108 | SOX11 | chr2:g.5700172A>C |
NM_003108 | SOX11 | chr2:g.5700200T>A |
NM_003108 | SOX11 | chr2:g.5696858C>T |
NM_003108 | SOX11 | chr2:g.5695971G>C |
NM_003108 | SOX11 | chr2:g.5694500G>T |
NM_003108 | SOX11 | chr2:g.5700201G>T |
NM_003108 | SOX11 | chr2:g.5697838C>T |
NM_003108 | SOX11 | chr2:g.5697645G>T |
NM_003108 | SOX11 | chr2:g.5697533C>A |
NM_003108 | SOX11 | chr2:g.5699290G>A |
NM_003108 | SOX11 | chr2:g.5699089G>C |
NM_003108 | SOX11 | chr2:g.5700103G>C |
NM_003108 | SOX11 | chr2:g.5695821T>A |
NM_003108 | SOX11 | chr2:g.5698906T>C |
NM_003108 | SOX11 | chr2:g.5695721C>T |
NM_003108 | SOX11 | chr2:g.5700123G>A |
NM_003108 | SOX11 | chr2:g.5700454A>G |
NM_003108 | SOX11 | chr2:g.5695352T>C |
NM_003108 | SOX11 | chr2:g.5698918T>G |
NM_003108 | SOX11 | chr2:g.5699974C>A |
NM_003108 | SOX11 | chr2:g.5695938G>T |
NM_003108 | SOX11 | chr2:g.5700676T>G |
NM_003108 | SOX11 | chr2:g.5697875A>C |
NM_003108 | SOX11 | chr2:g.5696561A>G |
NM_003108 | SOX11 | chr2:g.5698299A>C |