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 [80 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_004991 | MECOM | chr3:g.169083875T>G |
NM_004991 | MECOM | chr3:g.169084194T>C |
NM_004991 | MECOM | chr3:g.169084475T>C |
NM_004991 | MECOM | chr3:g.169182243G>A |
NM_004991 | MECOM | chr3:g.169268995C>A |
NM_004991 | MECOM | chr3:g.169279780A>C |
NM_004991 | MECOM | chr3:g.169349412T>C |
NM_004991 | MECOM | chr3:g.169363768G>A |
NM_004991 | MECOM | chr3:g.169365771G>A |
NM_004991 | MECOM | chr3:g.169483873C>G |
NM_004991 | MECOM | chr3:g.169504379A>G |
NM_004991 | MECOM | chr3:g.169530225T>C |
NM_004991 | MECOM | chr3:g.169561410C>G |
NM_004991 | MECOM | chr3:g.169561442A>T |
NM_004991 | MECOM | chr3:g.169626650A>G |
NM_004991 | MECOM | chr3:g.169647462T>C |
NM_004991 | MECOM | chr3:g.169648705G>C |
NM_004991 | MECOM | chr3:g.169648915T>A |
NM_004991 | MECOM | chr3:g.169654098A>G |
NM_004991 | MECOM | chr3:g.169657820G>A |
NM_004991 | MECOM | chr3:g.169658120C>T |
NM_004991 | MECOM | chr3:g.169659715C>G |
NM_004991 | MECOM | chr3:g.169661094C>A |
NM_004991 | MECOM | chr3:g.169662777G>CGGG |
NM_004991 | MECOM | chr3:g.169663304T>C |
NM_004991 | MECOM | chr3:g.169663602G>T |
NM_004991 | MECOM | chr3:g.169084922T>C |
NM_004991 | MECOM | chr3:g.169084935G>T |
NM_004991 | MECOM | chr3:g.169084945G>A |
NM_004991 | MECOM | chr3:g.169084948G>A |
NM_004991 | MECOM | chr3:g.169084949C>T |
NM_004991 | MECOM | chr3:g.169090005A>G |
NM_004991 | MECOM | chr3:g.169090033C>T |
NM_004991 | MECOM | chr3:g.169093056G>A |
NM_004991 | MECOM | chr3:g.169093060G>C |
NM_004991 | MECOM | chr3:g.169093061G>A |
NM_004991 | MECOM | chr3:g.169093070G>A |
NM_004991 | MECOM | chr3:g.169095082A>G |
NM_004991 | MECOM | chr3:g.169095089T>A |
NM_004991 | MECOM | chr3:g.169095092G>A |
NM_004991 | MECOM | chr3:g.169095094G>A |
NM_004991 | MECOM | chr3:g.169100919GGC>AAC |
NM_004991 | MECOM | chr3:g.169100921G>A |
NM_004991 | MECOM | chr3:g.169100938G>A |
NM_004991 | MECOM | chr3:g.169100943C>T |
NM_004991 | MECOM | chr3:g.169102087G>A |
NM_004991 | MECOM | chr3:g.169102122G>T |
NM_004991 | MECOM | chr3:g.169102160G>A |
NM_004991 | MECOM | chr3:g.169102176G>A |
NM_004991 | MECOM | chr3:g.169102180C>T |
hsa_circ_0067877 | MECOM | chr3:g.169112831G>C |
hsa_circ_0067877 | MECOM | chr3:g.169112839C>A |
hsa_circ_0067877 | MECOM | chr3:g.169112852G>C |
hsa_circ_0067877 | MECOM | chr3:g.169112853T>C |
hsa_circ_0067877 | MECOM | chr3:g.169115721G>A |
hsa_circ_0067877 | MECOM | chr3:g.169115722C>T |
hsa_circ_0067877 | MECOM | chr3:g.169115723T>C |
hsa_circ_0067877 | MECOM | chr3:g.169115741C>T |
hsa_circ_0067877 | MECOM | chr3:g.169115751G>A |
hsa_circ_0067877 | MECOM | chr3:g.169115753A>G |
hsa_circ_0067877 | MECOM | chr3:g.169115874T>C |
hsa_circ_0067877 | MECOM | chr3:g.169115894G>C |
hsa_circ_0067877 | MECOM | chr3:g.169115900G>T |
hsa_circ_0067877 | MECOM | chr3:g.169116275C>T |
hsa_circ_0067877 | MECOM | chr3:g.169116302CAAAA>A |
hsa_circ_0067877 | MECOM | chr3:g.169116380G>A |
hsa_circ_0067877 | MECOM | chr3:g.169116385C>T |
hsa_circ_0067877 | MECOM | chr3:g.169116386C>T |
hsa_circ_0067877 | MECOM | chr3:g.169116394G>C |
hsa_circ_0067877 | MECOM | chr3:g.169116397C>T |
hsa_circ_0067877 | MECOM | chr3:g.169121087G>A |
hsa_circ_0067877 | MECOM | chr3:g.169121105G>A |
hsa_circ_0067877 | MECOM | chr3:g.169121106C>T |
hsa_circ_0067877 | MECOM | chr3:g.169121108G>T |
hsa_circ_0067877 | MECOM | chr3:g.169121109C>T |
hsa_circ_0067877 | MECOM | chr3:g.169121151G>A |
hsa_circ_0067877 | MECOM | chr3:g.169121159C>T |
hsa_circ_0067877 | MECOM | chr3:g.169121181G>A |
NM_004991 | MECOM | chr3:g.169143748G>A |
NM_004991 | MECOM | chr3:g.169143749C>T |
Somatic mutations that alter predicted mRNA-miRNA target sites [42 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001105077 | MECOM | chr3:g.169084194T>C |
NM_001105078 | MECOM | chr3:g.169084194T>C |
NM_001163999 | MECOM | chr3:g.169084194T>C |
NM_001164000 | MECOM | chr3:g.169084194T>C |
NM_001205194 | MECOM | chr3:g.169084194T>C |
NM_004991 | MECOM | chr3:g.169084194T>C |
NM_005241 | MECOM | chr3:g.169084194T>C |
NM_001164000 | MECOM | chr3:g.169083875T>G |
NM_001105077 | MECOM | chr3:g.169083875T>G |
NM_001105078 | MECOM | chr3:g.169083875T>G |
NM_004991 | MECOM | chr3:g.169083875T>G |
NM_005241 | MECOM | chr3:g.169083875T>G |
NM_001163999 | MECOM | chr3:g.169083875T>G |
NM_001205194 | MECOM | chr3:g.169083875T>G |
NM_001164000 | MECOM | chr3:g.169084796C>A |
NM_001105077 | MECOM | chr3:g.169084796C>A |
NM_001105078 | MECOM | chr3:g.169084796C>A |
NM_004991 | MECOM | chr3:g.169084796C>A |
NM_005241 | MECOM | chr3:g.169084796C>A |
NM_001163999 | MECOM | chr3:g.169084796C>A |
NM_001205194 | MECOM | chr3:g.169084796C>A |
NM_001164000 | MECOM | chr3:g.169084297T>C |
NM_001105077 | MECOM | chr3:g.169084297T>C |
NM_001105078 | MECOM | chr3:g.169084297T>C |
NM_004991 | MECOM | chr3:g.169084297T>C |
NM_005241 | MECOM | chr3:g.169084297T>C |
NM_001163999 | MECOM | chr3:g.169084297T>C |
NM_001205194 | MECOM | chr3:g.169084297T>C |
NM_001164000 | MECOM | chr3:g.169084404G>A |
NM_001105077 | MECOM | chr3:g.169084404G>A |
NM_001105078 | MECOM | chr3:g.169084404G>A |
NM_004991 | MECOM | chr3:g.169084404G>A |
NM_005241 | MECOM | chr3:g.169084404G>A |
NM_001163999 | MECOM | chr3:g.169084404G>A |
NM_001205194 | MECOM | chr3:g.169084404G>A |
NM_001164000 | MECOM | chr3:g.169084475T>C |
NM_001105077 | MECOM | chr3:g.169084475T>C |
NM_001105078 | MECOM | chr3:g.169084475T>C |
NM_004991 | MECOM | chr3:g.169084475T>C |
NM_005241 | MECOM | chr3:g.169084475T>C |
NM_001163999 | MECOM | chr3:g.169084475T>C |
NM_001205194 | MECOM | chr3:g.169084475T>C |