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 [4 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001101654 | CXXC1 | chr18:g.50284040G>A |
NM_001101654 | CXXC1 | chr18:g.50284075G>A |
NM_001101654 | CXXC1 | chr18:g.50284078CA>A |
NM_001101654 | CXXC1 | chr18:g.50284082C>T |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [27 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0047680 | CXXC1 | chr18:g.50282502C>T |
NM_001101654 | CXXC1 | chr18:g.50287465G>A |
hsa_circ_0047680 | CXXC1 | chr18:g.50282598C>T |
hsa_circ_0047680 | CXXC1 | chr18:g.50282602C>T |
hsa_circ_0047680 | CXXC1 | chr18:g.50282606G>T |
hsa_circ_0047680 | CXXC1 | chr18:g.50282674G>T |
hsa_circ_0047680 | CXXC1 | chr18:g.50282675C>T |
hsa_circ_0047680 | CXXC1 | chr18:g.50282676G>A |
hsa_circ_0047680 | CXXC1 | chr18:g.50282677C>T |
hsa_circ_0047680 | CXXC1 | chr18:g.50282687T>C |
hsa_circ_0047681 | CXXC1 | chr18:g.50283799G>T |
hsa_circ_0047682 | CXXC1 | chr18:g.50284075G>A |
hsa_circ_0047682 | CXXC1 | chr18:g.50284078CA>A |
hsa_circ_0047682 | CXXC1 | chr18:g.50284082C>T |
hsa_circ_0047681 | CXXC1 | chr18:g.50284544C>T |
hsa_circ_0047683 | CXXC1 | chr18:g.50285101G>T |
hsa_circ_0047681 | CXXC1 | chr18:g.50286108G>T |
hsa_circ_0047681 | CXXC1 | chr18:g.50286155G>A |
hsa_circ_0047681 | CXXC1 | chr18:g.50286156C>T |
hsa_circ_0047681 | CXXC1 | chr18:g.50286159G>A |
hsa_circ_0047681 | CXXC1 | chr18:g.50286174C>T |
hsa_circ_0047681 | CXXC1 | chr18:g.50286192C>T |
hsa_circ_0047681 | CXXC1 | chr18:g.50286234C>T |
hsa_circ_0047681 | CXXC1 | chr18:g.50286609T>C |
NM_001101654 | CXXC1 | chr18:g.50286763A>C |
NM_001101654 | CXXC1 | chr18:g.50286780T>C |
NM_001101654 | CXXC1 | chr18:g.50286822G>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [8 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001101654 | CXXC1 | chr18:g.50282502C>T |
NM_014593 | CXXC1 | chr18:g.50282502C>T |
NM_001101654 | CXXC1 | chr18:g.50282580G>A |
NM_014593 | CXXC1 | chr18:g.50282580G>A |
NM_001101654 | CXXC1 | chr18:g.50282436C>T |
NM_014593 | CXXC1 | chr18:g.50282436C>T |
NM_001101654 | CXXC1 | chr18:g.50282579G>T |
NM_014593 | CXXC1 | chr18:g.50282579G>T |