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 [55 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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NM_001024688 | NBN | chr8:g.89935439A>G |
hsa_circ_0084866 | NBN | chr8:g.89943253G>A |
hsa_circ_0084866 | NBN | chr8:g.89953261G>A |
hsa_circ_0084866 | NBN | chr8:g.89953462G>A |
hsa_circ_0084866 | NBN | chr8:g.89953471C>A |
hsa_circ_0084866 | NBN | chr8:g.89953471C>T |
hsa_circ_0084866 | NBN | chr8:g.89953618G>T |
hsa_circ_0084866 | NBN | chr8:g.89953619TA>A |
hsa_circ_0084866 | NBN | chr8:g.89953625T>G |
hsa_circ_0084866 | NBN | chr8:g.89953631T>C |
hsa_circ_0084866 | NBN | chr8:g.89953635C>T |
hsa_circ_0084866 | NBN | chr8:g.89955290A>G |
hsa_circ_0084866 | NBN | chr8:g.89955384A>G |
hsa_circ_0084866 | NBN | chr8:g.89955386T>C |
hsa_circ_0084866 | NBN | chr8:g.89955427C>G |
hsa_circ_0084866 | NBN | chr8:g.89955427C>A |
hsa_circ_0084866 | NBN | chr8:g.89955483T>C |
hsa_circ_0084866 | NBN | chr8:g.89955499G>T |
hsa_circ_0084866 | NBN | chr8:g.89955515A>G |
hsa_circ_0084866 | NBN | chr8:g.89955520C>T |
hsa_circ_0084866 | NBN | chr8:g.89958734C>T |
hsa_circ_0084866 | NBN | chr8:g.89958760C>T |
hsa_circ_0084866 | NBN | chr8:g.89958762T>C |
hsa_circ_0084866 | NBN | chr8:g.89964425G>T |
hsa_circ_0084866 | NBN | chr8:g.89964439A>G |
hsa_circ_0084866 | NBN | chr8:g.89964440T>C |
hsa_circ_0084866 | NBN | chr8:g.89964456C>A |
hsa_circ_0084866 | NBN | chr8:g.89970536G>C |
hsa_circ_0084866 | NBN | chr8:g.89970540C>T |
hsa_circ_0084866 | NBN | chr8:g.89971173G>T |
hsa_circ_0084866 | NBN | chr8:g.89971185G>T |
hsa_circ_0084866 | NBN | chr8:g.89971204G>C |
hsa_circ_0084866 | NBN | chr8:g.89971209C>T |
hsa_circ_0084866 | NBN | chr8:g.89971217C>G |
hsa_circ_0084866 | NBN | chr8:g.89971218A>T |
hsa_circ_0084866 | NBN | chr8:g.89978247C>T |
hsa_circ_0084866 | NBN | chr8:g.89978251G>A |
hsa_circ_0084866 | NBN | chr8:g.89978251G>T |
hsa_circ_0084866 | NBN | chr8:g.89978251G>C |
hsa_circ_0084866 | NBN | chr8:g.89978263C>A |
NM_001024688 | NBN | chr8:g.89980755A>G |
NM_001024688 | NBN | chr8:g.89980789A>G |
NM_001024688 | NBN | chr8:g.89980810T>C |
NM_001024688 | NBN | chr8:g.89980821T>C |
NM_001024688 | NBN | chr8:g.89980822C>A |
NM_001024688 | NBN | chr8:g.89980848C>G |
NM_001024688 | NBN | chr8:g.89980852AGA>GAA |
NM_001024688 | NBN | chr8:g.89980889G>A |
NM_001024688 | NBN | chr8:g.89981386GA>A |
NM_001024688 | NBN | chr8:g.89981491A>G |
NM_001024688 | NBN | chr8:g.89982731A>T |
NM_001024688 | NBN | chr8:g.89982765G>A |
NM_001024688 | NBN | chr8:g.89982770C>T |
NM_001024688 | NBN | chr8:g.89982786A>C |
NM_001024688 | NBN | chr8:g.89982789T>C |
Somatic mutations that alter predicted mRNA-miRNA target sites [3 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_002485 | NBN | chr8:g.89935096T>A |
NM_002485 | NBN | chr8:g.89935439A>G |
NM_002485 | NBN | chr8:g.89934415A>G |