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 [23 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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hsa_circ_0057700 | SPATS2L | chr2:g.200412381A>G |
hsa_circ_0057700 | SPATS2L | chr2:g.200412385T>G |
hsa_circ_0057700 | SPATS2L | chr2:g.200412400C>A |
hsa_circ_0057700 | SPATS2L | chr2:g.200419250A>G |
hsa_circ_0057700 | SPATS2L | chr2:g.200419254A>G |
hsa_circ_0057700 | SPATS2L | chr2:g.200419385G>A |
hsa_circ_0057700 | SPATS2L | chr2:g.200419398C>T |
hsa_circ_0057700 | SPATS2L | chr2:g.200419417C>T |
hsa_circ_0057700 | SPATS2L | chr2:g.200419418G>A |
hsa_circ_0057700 | SPATS2L | chr2:g.200439198A>C |
hsa_circ_0057700 | SPATS2L | chr2:g.200439211T>TGGTC |
hsa_circ_0057700 | SPATS2L | chr2:g.200440660G>C |
hsa_circ_0057700 | SPATS2L | chr2:g.200440684C>T |
hsa_circ_0057700 | SPATS2L | chr2:g.200459808T>C |
hsa_circ_0057700 | SPATS2L | chr2:g.200467358A>G |
hsa_circ_0057700 | SPATS2L | chr2:g.200472874G>T |
hsa_circ_0057700 | SPATS2L | chr2:g.200472943C>A |
hsa_circ_0057700 | SPATS2L | chr2:g.200472951C>T |
hsa_circ_0057700 | SPATS2L | chr2:g.200472952A>G |
hsa_circ_0057700 | SPATS2L | chr2:g.200472955A>G |
NM_001282735 | SPATS2L | chr2:g.200477719T>G |
NM_001282735 | SPATS2L | chr2:g.200477832C>T |
NM_001282735 | SPATS2L | chr2:g.200477847C>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [16 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_015535 | SPATS2L | chr2:g.200482040A>G |
NM_001100424 | SPATS2L | chr2:g.200482040A>G |
NM_001100423 | SPATS2L | chr2:g.200482040A>G |
NM_001100422 | SPATS2L | chr2:g.200482040A>G |
NM_015535 | SPATS2L | chr2:g.200482042G>A |
NM_001100424 | SPATS2L | chr2:g.200482042G>A |
NM_001100423 | SPATS2L | chr2:g.200482042G>A |
NM_001100422 | SPATS2L | chr2:g.200482042G>A |
NM_015535 | SPATS2L | chr2:g.200478912T>C |
NM_001100424 | SPATS2L | chr2:g.200478912T>C |
NM_001100423 | SPATS2L | chr2:g.200478912T>C |
NM_001100422 | SPATS2L | chr2:g.200478912T>C |
NM_015535 | SPATS2L | chr2:g.200480143A>G |
NM_001100424 | SPATS2L | chr2:g.200480143A>G |
NM_001100423 | SPATS2L | chr2:g.200480143A>G |
NM_001100422 | SPATS2L | chr2:g.200480143A>G |