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: CLASH [23 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_002467 | MYC | chr8:g.127741083A>C |
NM_002467 | MYC | chr8:g.127741086C>A |
NM_002467 | MYC | chr8:g.127741090A>G |
NM_002467 | MYC | chr8:g.127738266C>T |
NM_002467 | MYC | chr8:g.127738270T>G |
NM_002467 | MYC | chr8:g.127738275G>A |
NM_002467 | MYC | chr8:g.127738276T>C |
NM_002467 | MYC | chr8:g.127738279G>C |
NM_002467 | MYC | chr8:g.127738279G>A |
NM_002467 | MYC | chr8:g.127738280C>G |
NM_002467 | MYC | chr8:g.127738281T>C |
NM_002467 | MYC | chr8:g.127738283C>G |
NM_002467 | MYC | chr8:g.127738283C>A |
NM_002467 | MYC | chr8:g.127738289C>G |
NM_002467 | MYC | chr8:g.127738297A>C |
NM_002467 | MYC | chr8:g.127738297A>G |
NM_002467 | MYC | chr8:g.127738302C>G |
NM_002467 | MYC | chr8:g.127738308T>C |
NM_002467 | MYC | chr8:g.127738837C>T |
NM_002467 | MYC | chr8:g.127738848C>T |
NM_002467 | MYC | chr8:g.127738861A>T |
NM_002467 | MYC | chr8:g.127738870G>C |
NM_002467 | MYC | chr8:g.127738910C>T |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [74 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0085534 | MYC | chr8:g.127736222G>A |
hsa_circ_0085534 | MYC | chr8:g.127736229C>G |
hsa_circ_0085534 | MYC | chr8:g.127736311C>G |
hsa_circ_0085534 | MYC | chr8:g.127736341C>T |
hsa_circ_0085534 | MYC | chr8:g.127736357G>A |
hsa_circ_0085534 | MYC | chr8:g.127736375C>T |
hsa_circ_0085534 | MYC | chr8:g.127736448C>T |
hsa_circ_0085535 | MYC | chr8:g.127741026A>C |
hsa_circ_0085535 | MYC | chr8:g.127741064T>C |
hsa_circ_0085535 | MYC | chr8:g.127741083A>C |
hsa_circ_0085535 | MYC | chr8:g.127741086C>A |
hsa_circ_0085535 | MYC | chr8:g.127741090A>G |
hsa_circ_0085535 | MYC | chr8:g.127741277C>A |
hsa_circ_0085535 | MYC | chr8:g.127738249A>G |
hsa_circ_0085535 | MYC | chr8:g.127738266C>T |
hsa_circ_0085535 | MYC | chr8:g.127738270T>G |
hsa_circ_0085535 | MYC | chr8:g.127738275G>A |
hsa_circ_0085535 | MYC | chr8:g.127738276T>C |
hsa_circ_0085535 | MYC | chr8:g.127738279G>C |
hsa_circ_0085535 | MYC | chr8:g.127738279G>A |
hsa_circ_0085535 | MYC | chr8:g.127738280C>G |
hsa_circ_0085535 | MYC | chr8:g.127738281T>C |
hsa_circ_0085535 | MYC | chr8:g.127738283C>G |
hsa_circ_0085535 | MYC | chr8:g.127738283C>A |
hsa_circ_0085535 | MYC | chr8:g.127738289C>G |
hsa_circ_0085535 | MYC | chr8:g.127738297A>C |
hsa_circ_0085535 | MYC | chr8:g.127738297A>G |
hsa_circ_0085535 | MYC | chr8:g.127738302C>G |
hsa_circ_0085535 | MYC | chr8:g.127738308T>C |
hsa_circ_0085535 | MYC | chr8:g.127738489C>T |
hsa_circ_0085535 | MYC | chr8:g.127738491G>A |
hsa_circ_0085535 | MYC | chr8:g.127738493C>G |
hsa_circ_0085535 | MYC | chr8:g.127738506C>G |
hsa_circ_0085535 | MYC | chr8:g.127738631C>T |
hsa_circ_0085535 | MYC | chr8:g.127738634C>T |
hsa_circ_0085535 | MYC | chr8:g.127738640A>C |
hsa_circ_0085535 | MYC | chr8:g.127738647A>G |
hsa_circ_0085535 | MYC | chr8:g.127738674T>C |
hsa_circ_0085535 | MYC | chr8:g.127738675T>G |
hsa_circ_0085535 | MYC | chr8:g.127738675T>C |
hsa_circ_0085535 | MYC | chr8:g.127738682C>A |
hsa_circ_0085535 | MYC | chr8:g.127738683G>T |
hsa_circ_0085535 | MYC | chr8:g.127738683G>A |
hsa_circ_0085535 | MYC | chr8:g.127738741G>A |
hsa_circ_0085535 | MYC | chr8:g.127738747C>G |
hsa_circ_0085535 | MYC | chr8:g.127738755G>A |
hsa_circ_0085535 | MYC | chr8:g.127738759G>A |
hsa_circ_0085535 | MYC | chr8:g.127738769C>A |
hsa_circ_0085535 | MYC | chr8:g.127738774G>C |
hsa_circ_0085535 | MYC | chr8:g.127738781C>T |
hsa_circ_0085535 | MYC | chr8:g.127738786G>C |
hsa_circ_0085535 | MYC | chr8:g.127738790G>A |
hsa_circ_0085535 | MYC | chr8:g.127738848C>T |
hsa_circ_0085535 | MYC | chr8:g.127738861A>T |
hsa_circ_0085535 | MYC | chr8:g.127740538C>T |
hsa_circ_0085535 | MYC | chr8:g.127740554C>G |
hsa_circ_0085535 | MYC | chr8:g.127740556G>A |
hsa_circ_0085535 | MYC | chr8:g.127740573C>T |
hsa_circ_0085535 | MYC | chr8:g.127740579C>T |
hsa_circ_0085535 | MYC | chr8:g.127740580C>T |
hsa_circ_0085535 | MYC | chr8:g.127740585G>T |
hsa_circ_0085535 | MYC | chr8:g.127740600C>T |
hsa_circ_0085535 | MYC | chr8:g.127740634C>T |
hsa_circ_0085535 | MYC | chr8:g.127740635C>G |
hsa_circ_0085535 | MYC | chr8:g.127740636T>C |
hsa_circ_0085535 | MYC | chr8:g.127740637G>A |
hsa_circ_0085535 | MYC | chr8:g.127740844C>T |
hsa_circ_0085535 | MYC | chr8:g.127740848C>A |
hsa_circ_0085535 | MYC | chr8:g.127740851T>A |
hsa_circ_0085535 | MYC | chr8:g.127740884G>A |
hsa_circ_0085535 | MYC | chr8:g.127740945ACT>A |
hsa_circ_0085535 | MYC | chr8:g.127740951G>C |
hsa_circ_0085535 | MYC | chr8:g.127740955G>T |
hsa_circ_0085535 | MYC | chr8:g.127740955G>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [8 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_002467 | MYC | chr8:g.127741277C>A |
NM_002467 | MYC | chr8:g.127741008A>G |
NM_002467 | MYC | chr8:g.127741314A>C |
NM_002467 | MYC | chr8:g.127741026A>C |
NM_002467 | MYC | chr8:g.127741083A>C |
NM_002467 | MYC | chr8:g.127741086C>A |
NM_002467 | MYC | chr8:g.127741064T>C |
NM_002467 | MYC | chr8:g.127741090A>G |