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 [89 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0074058 | SPOCK1 | chr5:g.136975441C>A |
hsa_circ_0074058 | SPOCK1 | chr5:g.136975528C>G |
hsa_circ_0074058 | SPOCK1 | chr5:g.136975691C>T |
hsa_circ_0074058 | SPOCK1 | chr5:g.136976006T>A |
hsa_circ_0074058 | SPOCK1 | chr5:g.136976718T>A |
hsa_circ_0074058 | SPOCK1 | chr5:g.136976744C>T |
hsa_circ_0074058 | SPOCK1 | chr5:g.136976911T>C |
hsa_circ_0074058 | SPOCK1 | chr5:g.136977128T>C |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978306A>G |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978446T>G |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978629T>G |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978756CA>A |
NM_004598 | SPOCK1 | chr5:g.137031832A>G |
NM_004598 | SPOCK1 | chr5:g.137032569A>G |
hsa_circ_0074059 | SPOCK1 | chr5:g.137098577C>A |
hsa_circ_0074061 | SPOCK1 | chr5:g.137125155A>C |
hsa_circ_0074061 | SPOCK1 | chr5:g.137163257T>G |
hsa_circ_0074061 | SPOCK1 | chr5:g.137205391G>A |
hsa_circ_0074061 | SPOCK1 | chr5:g.137261917C>A |
NM_004598 | SPOCK1 | chr5:g.137370434C>A |
NM_004598 | SPOCK1 | chr5:g.137370471C>A |
NM_004598 | SPOCK1 | chr5:g.137387787C>G |
NM_004598 | SPOCK1 | chr5:g.137389625G>A |
NM_004598 | SPOCK1 | chr5:g.137395353G>A |
NM_004598 | SPOCK1 | chr5:g.137416133G>A |
NM_004598 | SPOCK1 | chr5:g.137444105A>C |
NM_004598 | SPOCK1 | chr5:g.137457410C>G |
NM_004598 | SPOCK1 | chr5:g.137459828A>G |
NM_004598 | SPOCK1 | chr5:g.137462019A>T |
NM_004598 | SPOCK1 | chr5:g.137490460G>A |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978669C>T |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978762G>T |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978769G>A |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978770C>T |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978788TGG>TCG |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978798G>C |
hsa_circ_0074058 | SPOCK1 | chr5:g.136978804G>T |
hsa_circ_0074058 | SPOCK1 | chr5:g.136979336C>G |
hsa_circ_0074058 | SPOCK1 | chr5:g.136979340T>C |
hsa_circ_0074058 | SPOCK1 | chr5:g.136979344G>A |
NM_004598 | SPOCK1 | chr5:g.136988457A>C |
NM_004598 | SPOCK1 | chr5:g.136988457A>G |
NM_004598 | SPOCK1 | chr5:g.136988466A>C |
NM_004598 | SPOCK1 | chr5:g.136988469G>A |
NM_004598 | SPOCK1 | chr5:g.136988480C>T |
NM_004598 | SPOCK1 | chr5:g.136988482T>A |
NM_004598 | SPOCK1 | chr5:g.136988494A>T |
NM_004598 | SPOCK1 | chr5:g.136988507C>T |
NM_004598 | SPOCK1 | chr5:g.136988519C>G |
NM_004598 | SPOCK1 | chr5:g.136988523A>T |
NM_004598 | SPOCK1 | chr5:g.136988523A>C |
NM_004598 | SPOCK1 | chr5:g.136988528G>A |
NM_004598 | SPOCK1 | chr5:g.136988535T>A |
NM_004598 | SPOCK1 | chr5:g.136988550C>G |
NM_004598 | SPOCK1 | chr5:g.136988557G>C |
NM_004598 | SPOCK1 | chr5:g.136988574A>C |
NM_004598 | SPOCK1 | chr5:g.136988576G>A |
NM_004598 | SPOCK1 | chr5:g.136988584T>C |
NM_004598 | SPOCK1 | chr5:g.136988600C>A |
NM_004598 | SPOCK1 | chr5:g.136988600GC>C |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067748C>T |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067762C>T |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067769C>T |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067777G>A |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067784A>T |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067787G>A |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067788C>T |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067791C>G |
hsa_circ_0074059 | SPOCK1 | chr5:g.137067814C>G |
hsa_circ_0074061 | SPOCK1 | chr5:g.137112448C>A |
hsa_circ_0074061 | SPOCK1 | chr5:g.137112486G>T |
hsa_circ_0074061 | SPOCK1 | chr5:g.137112488G>A |
hsa_circ_0074061 | SPOCK1 | chr5:g.137112488CCG>TTG |
hsa_circ_0074061 | SPOCK1 | chr5:g.137112490C>T |
hsa_circ_0074061 | SPOCK1 | chr5:g.137112494T>G |
hsa_circ_0074061 | SPOCK1 | chr5:g.137112497C>T |
hsa_circ_0074061 | SPOCK1 | chr5:g.137140598G>A |
hsa_circ_0074061 | SPOCK1 | chr5:g.137140611C>A |
hsa_circ_0074061 | SPOCK1 | chr5:g.137140614G>A |
hsa_circ_0074061 | SPOCK1 | chr5:g.137140627G>T |
hsa_circ_0074061 | SPOCK1 | chr5:g.137140629C>T |
hsa_circ_0074061 | SPOCK1 | chr5:g.137140631C>T |
NM_004598 | SPOCK1 | chr5:g.137498417G>A |
NM_004598 | SPOCK1 | chr5:g.137498458A>G |
NM_004598 | SPOCK1 | chr5:g.137498474G>A |
NM_004598 | SPOCK1 | chr5:g.137498475C>T |
NM_004598 | SPOCK1 | chr5:g.137498478C>G |
NM_004598 | SPOCK1 | chr5:g.137498484C>T |
NM_004598 | SPOCK1 | chr5:g.137498528G>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [17 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_004598 | SPOCK1 | chr5:g.136976718T>A |
NM_004598 | SPOCK1 | chr5:g.136975441C>A |
NM_004598 | SPOCK1 | chr5:g.136976744C>T |
NM_004598 | SPOCK1 | chr5:g.136978446T>G |
NM_004598 | SPOCK1 | chr5:g.136978324A>C |
NM_004598 | SPOCK1 | chr5:g.136977098T>C |
NM_004598 | SPOCK1 | chr5:g.136976350T>C |
NM_004598 | SPOCK1 | chr5:g.136978329G>T |
NM_004598 | SPOCK1 | chr5:g.136976911T>C |
NM_004598 | SPOCK1 | chr5:g.136978306A>G |
NM_004598 | SPOCK1 | chr5:g.136977128T>C |
NM_004598 | SPOCK1 | chr5:g.136975528C>G |
NM_004598 | SPOCK1 | chr5:g.136977613G>C |
NM_004598 | SPOCK1 | chr5:g.136976006T>A |
NM_004598 | SPOCK1 | chr5:g.136976495G>A |
NM_004598 | SPOCK1 | chr5:g.136976144A>G |
NM_004598 | SPOCK1 | chr5:g.136975691C>T |