SomamiR DB 2.0
Somatic mutations altering microRNA-ceRNA interactions
  Home Search Help Download  


Browse genes associated with cancer risk that contain miRNA related somatic mutations


Somatic mutations that alter miRNA target sites: CLASH [8 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_015335 MED13L chr12:g.115986398G>A
NM_015335 MED13L chr12:g.115986399C>T
NM_015335 MED13L chr12:g.115986405C>T
NM_015335 MED13L chr12:g.115986412C>T
NM_015335 MED13L chr12:g.115991493A>T
NM_015335 MED13L chr12:g.115991525G>A
NM_015335 MED13L chr12:g.115991526C>T
NM_015335 MED13L chr12:g.115991528G>A



Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [83 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
hsa_circ_0028549 MED13L chr12:g.115960775C>T
hsa_circ_0028549 MED13L chr12:g.115961089T>C
hsa_circ_0028549 MED13L chr12:g.115961330C>T
hsa_circ_0028549 MED13L chr12:g.115961350G>A
hsa_circ_0028549 MED13L chr12:g.115961350G>T
hsa_circ_0028549 MED13L chr12:g.115961360C>T
hsa_circ_0028555 MED13L chr12:g.115969027C>T
hsa_circ_0028555 MED13L chr12:g.115969030G>A
hsa_circ_0028555 MED13L chr12:g.115970629A>T
hsa_circ_0028555 MED13L chr12:g.115970653C>T
hsa_circ_0028559 MED13L chr12:g.115975284A>C
hsa_circ_0028563 MED13L chr12:g.115975540G>A
hsa_circ_0028563 MED13L chr12:g.115975549G>C
hsa_circ_0028564 MED13L chr12:g.115980793T>C
hsa_circ_0028564 MED13L chr12:g.115980799C>T
hsa_circ_0028564 MED13L chr12:g.115980806T>C
hsa_circ_0028564 MED13L chr12:g.115980854G>A
hsa_circ_0028565 MED13L chr12:g.115982483GGAC>C
hsa_circ_0028565 MED13L chr12:g.115983328T>A
hsa_circ_0028565 MED13L chr12:g.115983331G>A
hsa_circ_0028565 MED13L chr12:g.115983498T>C
hsa_circ_0028565 MED13L chr12:g.115983499A>G
hsa_circ_0028568 MED13L chr12:g.115984199A>C
hsa_circ_0028568 MED13L chr12:g.115984203C>T
hsa_circ_0028571 MED13L chr12:g.115987121C>T
hsa_circ_0028571 MED13L chr12:g.115987188G>A
hsa_circ_0028571 MED13L chr12:g.115987191C>T
hsa_circ_0028571 MED13L chr12:g.115991174T>C
hsa_circ_0028571 MED13L chr12:g.115991190C>T
hsa_circ_0028571 MED13L chr12:g.115991197A>T
hsa_circ_0028571 MED13L chr12:g.115991238C>A
hsa_circ_0028571 MED13L chr12:g.115991242G>T
hsa_circ_0028571 MED13L chr12:g.115991254A>T
hsa_circ_0028571 MED13L chr12:g.115991260C>G
hsa_circ_0028571 MED13L chr12:g.115991398A>G
hsa_circ_0028571 MED13L chr12:g.115991422C>T
hsa_circ_0028571 MED13L chr12:g.115991442A>C
hsa_circ_0028571 MED13L chr12:g.115991550C>T
hsa_circ_0028571 MED13L chr12:g.115991565G>A
hsa_circ_0028571 MED13L chr12:g.115991605G>A
hsa_circ_0028571 MED13L chr12:g.115991611C>G
hsa_circ_0028571 MED13L chr12:g.115991611C>T
hsa_circ_0028571 MED13L chr12:g.115991904A>T
hsa_circ_0028573 MED13L chr12:g.115996555C>T
hsa_circ_0028573 MED13L chr12:g.115996563G>A
hsa_circ_0028573 MED13L chr12:g.115996601G>A
hsa_circ_0028573 MED13L chr12:g.115996608T>G
hsa_circ_0028573 MED13L chr12:g.115996674C>A
hsa_circ_0028573 MED13L chr12:g.115997032G>T
hsa_circ_0028573 MED13L chr12:g.115997101G>A
hsa_circ_0028573 MED13L chr12:g.116005919C>T
hsa_circ_0028573 MED13L chr12:g.116005947T>C
hsa_circ_0028573 MED13L chr12:g.116005964G>A
hsa_circ_0028573 MED13L chr12:g.116005968C>T
hsa_circ_0028573 MED13L chr12:g.116005986G>T
hsa_circ_0028573 MED13L chr12:g.116006340T>G
hsa_circ_0028573 MED13L chr12:g.116006346G>A
hsa_circ_0028578 MED13L chr12:g.116007485G>A
hsa_circ_0028578 MED13L chr12:g.116007488G>A
hsa_circ_0028578 MED13L chr12:g.116007546A>G
hsa_circ_0028578 MED13L chr12:g.116007596G>T
hsa_circ_0028578 MED13L chr12:g.116008433G>T
hsa_circ_0028578 MED13L chr12:g.116008610C>T
hsa_circ_0028578 MED13L chr12:g.116008612C>T
hsa_circ_0028578 MED13L chr12:g.116008640G>A
hsa_circ_0028578 MED13L chr12:g.116008822G>A
hsa_circ_0028578 MED13L chr12:g.116008856G>T
hsa_circ_0028578 MED13L chr12:g.116008899G>C
hsa_circ_0028578 MED13L chr12:g.116008920G>T
hsa_circ_0028578 MED13L chr12:g.116008930G>A
hsa_circ_0028578 MED13L chr12:g.116009007C>T
hsa_circ_0028578 MED13L chr12:g.116009015G>A
hsa_circ_0028578 MED13L chr12:g.116009095C>T
hsa_circ_0028579 MED13L chr12:g.116015155G>A
hsa_circ_0028579 MED13L chr12:g.116015156G>TG
hsa_circ_0028579 MED13L chr12:g.116015163A>G
hsa_circ_0028579 MED13L chr12:g.116015190C>T
hsa_circ_0028582 MED13L chr12:g.116019851AG>G
hsa_circ_0028582 MED13L chr12:g.116019866G>A
hsa_circ_0028582 MED13L chr12:g.116019869C>T
hsa_circ_0028582 MED13L chr12:g.116019941G>A
hsa_circ_0028582 MED13L chr12:g.116019942C>T
hsa_circ_0028585 MED13L chr12:g.116084980A>G



Somatic mutations that alter predicted mRNA-miRNA target sites [9 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_015335 MED13L chr12:g.115959344C>T
NM_015335 MED13L chr12:g.115960063G>A
NM_015335 MED13L chr12:g.115960064G>T
NM_015335 MED13L chr12:g.115960276A>G
NM_015335 MED13L chr12:g.115960775C>T
NM_015335 MED13L chr12:g.115960960C>T
NM_015335 MED13L chr12:g.115960961G>A
NM_015335 MED13L chr12:g.115960992G>A
NM_015335 MED13L chr12:g.115961089T>C