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 [67 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0027489 | MDM2 | chr12:g.68809063G>A |
NM_001145339 | MDM2 | chr12:g.68840922G>T |
NM_001145339 | MDM2 | chr12:g.68808481G>C |
NM_001145339 | MDM2 | chr12:g.68808487A>C |
hsa_circ_0027489 | MDM2 | chr12:g.68809215T>C |
hsa_circ_0027489 | MDM2 | chr12:g.68809231C>G |
hsa_circ_0027489 | MDM2 | chr12:g.68809240C>T |
hsa_circ_0027489 | MDM2 | chr12:g.68813586A>G |
hsa_circ_0027489 | MDM2 | chr12:g.68813600C>A |
hsa_circ_0027489 | MDM2 | chr12:g.68816849G>A |
hsa_circ_0027489 | MDM2 | chr12:g.68816863A>C |
hsa_circ_0027489 | MDM2 | chr12:g.68816893G>T |
hsa_circ_0027489 | MDM2 | chr12:g.68816908T>G |
hsa_circ_0027489 | MDM2 | chr12:g.68820329A>G |
hsa_circ_0027489 | MDM2 | chr12:g.68828813G>A |
hsa_circ_0027489 | MDM2 | chr12:g.68828830A>G |
hsa_circ_0027489 | MDM2 | chr12:g.68828834C>T |
hsa_circ_0027489 | MDM2 | chr12:g.68828856G>A |
hsa_circ_0027489 | MDM2 | chr12:g.68828861T>C |
hsa_circ_0027489 | MDM2 | chr12:g.68828861T>A |
hsa_circ_0027489 | MDM2 | chr12:g.68828877G>T |
hsa_circ_0027489 | MDM2 | chr12:g.68828909C>G |
hsa_circ_0027489 | MDM2 | chr12:g.68828911A>T |
hsa_circ_0027489 | MDM2 | chr12:g.68828918C>T |
hsa_circ_0027489 | MDM2 | chr12:g.68828925G>A |
hsa_circ_0027489 | MDM2 | chr12:g.68835845T>C |
hsa_circ_0027489 | MDM2 | chr12:g.68835848G>A |
hsa_circ_0027489 | MDM2 | chr12:g.68835850G>C |
hsa_circ_0027489 | MDM2 | chr12:g.68835924C>T |
hsa_circ_0027489 | MDM2 | chr12:g.68835925G>A |
hsa_circ_0027489 | MDM2 | chr12:g.68835954A>G |
hsa_circ_0027489 | MDM2 | chr12:g.68835956G>A |
hsa_circ_0002770 | MDM2 | chr12:g.68836684A>C |
hsa_circ_0002770 | MDM2 | chr12:g.68836690T>C |
hsa_circ_0002770 | MDM2 | chr12:g.68836691A>G |
hsa_circ_0002770 | MDM2 | chr12:g.68836692T>C |
NM_001145339 | MDM2 | chr12:g.68839301G>T |
NM_001145339 | MDM2 | chr12:g.68839309TC>T |
NM_001145339 | MDM2 | chr12:g.68839315C>T |
NM_001145339 | MDM2 | chr12:g.68839320C>T |
NM_001145339 | MDM2 | chr12:g.68839349C>T |
NM_001145339 | MDM2 | chr12:g.68839354G>T |
NM_001145339 | MDM2 | chr12:g.68839358T>G |
NM_001145339 | MDM2 | chr12:g.68839359G>T |
NM_001145339 | MDM2 | chr12:g.68839367G>A |
NM_001145339 | MDM2 | chr12:g.68839382G>A |
NM_001145339 | MDM2 | chr12:g.68839393A>C |
NM_001145339 | MDM2 | chr12:g.68839469A>G |
NM_001145339 | MDM2 | chr12:g.68839509A>G |
NM_001145339 | MDM2 | chr12:g.68839519T>C |
NM_001145339 | MDM2 | chr12:g.68839524A>G |
NM_001145339 | MDM2 | chr12:g.68839549A>G |
NM_001145339 | MDM2 | chr12:g.68839593G>A |
NM_001145339 | MDM2 | chr12:g.68839613T>A |
NM_001145339 | MDM2 | chr12:g.68839616G>C |
NM_001145339 | MDM2 | chr12:g.68839646A>T |
NM_001145339 | MDM2 | chr12:g.68839660T>G |
NM_001145339 | MDM2 | chr12:g.68839690G>A |
NM_001145339 | MDM2 | chr12:g.68839694T>A |
NM_001145339 | MDM2 | chr12:g.68839725T>C |
NM_001145339 | MDM2 | chr12:g.68839748A>T |
NM_001145339 | MDM2 | chr12:g.68839748A>G |
NM_001145339 | MDM2 | chr12:g.68839750G>T |
NM_001145339 | MDM2 | chr12:g.68839764G>A |
NM_001145339 | MDM2 | chr12:g.68839780G>T |
NM_001145339 | MDM2 | chr12:g.68839816A>G |
NM_001145339 | MDM2 | chr12:g.68839838T>C |
Somatic mutations that alter predicted mRNA-miRNA target sites [19 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_002392 | MDM2 | chr12:g.68845037T>G |
NM_002392 | MDM2 | chr12:g.68841030A>G |
NM_002392 | MDM2 | chr12:g.68840321C>T |
NM_002392 | MDM2 | chr12:g.68845024C>T |
NM_002392 | MDM2 | chr12:g.68844820A>G |
NM_002392 | MDM2 | chr12:g.68840170A>T |
NM_002392 | MDM2 | chr12:g.68844081T>G |
NM_002392 | MDM2 | chr12:g.68841109A>G |
NM_002392 | MDM2 | chr12:g.68841570G>- |
NM_002392 | MDM2 | chr12:g.68842543A>G |
NM_002392 | MDM2 | chr12:g.68842003A>C |
NM_002392 | MDM2 | chr12:g.68842743A>G |
NM_002392 | MDM2 | chr12:g.68844929C>T |
NM_002392 | MDM2 | chr12:g.68842995T>A |
NM_002392 | MDM2 | chr12:g.68845195T>G |
NM_002392 | MDM2 | chr12:g.68842860T>G |
NM_002392 | MDM2 | chr12:g.68840922G>T |
NM_002392 | MDM2 | chr12:g.68842498G>C |
NM_002392 | MDM2 | chr12:g.68842217C>A |