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 [3 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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NM_001184 | ATR | chr3:g.142549613C>G |
NM_001184 | ATR | chr3:g.142549649G>T |
NM_001184 | ATR | chr3:g.142549656A>G |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [53 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001184 | ATR | chr3:g.142449451T>G |
NM_001184 | ATR | chr3:g.142449454A>G |
NM_001184 | ATR | chr3:g.142449459G>C |
NM_001184 | ATR | chr3:g.142449460A>C |
NM_001184 | ATR | chr3:g.142449510A>G |
NM_001184 | ATR | chr3:g.142449511G>A |
hsa_circ_0067622 | ATR | chr3:g.142453128G>T |
hsa_circ_0067622 | ATR | chr3:g.142453137C>A |
hsa_circ_0067622 | ATR | chr3:g.142453150C>A |
hsa_circ_0067622 | ATR | chr3:g.142453154G>A |
hsa_circ_0067622 | ATR | chr3:g.142453164G>A |
hsa_circ_0067622 | ATR | chr3:g.142453165C>T |
hsa_circ_0067625 | ATR | chr3:g.142459346G>A |
hsa_circ_0067625 | ATR | chr3:g.142459350G>C |
hsa_circ_0067625 | ATR | chr3:g.142459356G>A |
hsa_circ_0067625 | ATR | chr3:g.142459357C>T |
hsa_circ_0067629 | ATR | chr3:g.142465222C>T |
hsa_circ_0067631 | ATR | chr3:g.142493194G>T |
hsa_circ_0067631 | ATR | chr3:g.142497144G>A |
hsa_circ_0067631 | ATR | chr3:g.142505239A>C |
hsa_circ_0067631 | ATR | chr3:g.142505264G>A |
hsa_circ_0067631 | ATR | chr3:g.142508062G>A |
hsa_circ_0067630 | ATR | chr3:g.142513589T>G |
hsa_circ_0067630 | ATR | chr3:g.142513591G>A |
hsa_circ_0067630 | ATR | chr3:g.142513601G>T |
hsa_circ_0067630 | ATR | chr3:g.142538492A>C |
hsa_circ_0067630 | ATR | chr3:g.142538522G>T |
hsa_circ_0067630 | ATR | chr3:g.142542684G>A |
hsa_circ_0067630 | ATR | chr3:g.142542698G>A |
hsa_circ_0067630 | ATR | chr3:g.142542706C>T |
hsa_circ_0067630 | ATR | chr3:g.142547820C>G |
hsa_circ_0067630 | ATR | chr3:g.142547837G>A |
hsa_circ_0067630 | ATR | chr3:g.142547839G>A |
hsa_circ_0067630 | ATR | chr3:g.142547850G>T |
hsa_circ_0067630 | ATR | chr3:g.142553867C>T |
hsa_circ_0067630 | ATR | chr3:g.142553869C>A |
hsa_circ_0067630 | ATR | chr3:g.142556409T>G |
hsa_circ_0067630 | ATR | chr3:g.142556410C>A |
hsa_circ_0067630 | ATR | chr3:g.142559338A>G |
hsa_circ_0067652 | ATR | chr3:g.142561362G>C |
hsa_circ_0067652 | ATR | chr3:g.142561371C>T |
hsa_circ_0067653 | ATR | chr3:g.142562435G>A |
hsa_circ_0067653 | ATR | chr3:g.142562491C>T |
hsa_circ_0067653 | ATR | chr3:g.142562509T>G |
hsa_circ_0067653 | ATR | chr3:g.142562525G>T |
hsa_circ_0067653 | ATR | chr3:g.142562546G>A |
hsa_circ_0067653 | ATR | chr3:g.142562758G>A |
hsa_circ_0067653 | ATR | chr3:g.142562769G>A |
hsa_circ_0067653 | ATR | chr3:g.142562770T>C |
hsa_circ_0067653 | ATR | chr3:g.142566127T>A |
hsa_circ_0067653 | ATR | chr3:g.142566142G>T |
hsa_circ_0067653 | ATR | chr3:g.142568103G>A |
hsa_circ_0067653 | ATR | chr3:g.142568134A>G |