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 [6 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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NM_015071 | ARHGAP26 | chr5:g.142776556G>A |
hsa_circ_0074365 | ARHGAP26 | chr5:g.142913213A>G |
hsa_circ_0074365 | ARHGAP26 | chr5:g.142913222C>G |
hsa_circ_0074365 | ARHGAP26 | chr5:g.142913236G>A |
hsa_circ_0074374 | ARHGAP26 | chr5:g.143207346G>A |
hsa_circ_0074374 | ARHGAP26 | chr5:g.143207364C>T |
Somatic mutations that alter predicted mRNA-miRNA target sites [38 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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NM_015071 | ARHGAP26 | chr5:g.143226304A>C |
NM_001135608 | ARHGAP26 | chr5:g.143226304A>C |
NM_001135608 | ARHGAP26 | chr5:g.143225226G>T |
NM_015071 | ARHGAP26 | chr5:g.143225226G>T |
NM_001135608 | ARHGAP26 | chr5:g.143226224A>G |
NM_015071 | ARHGAP26 | chr5:g.143226224A>G |
NM_001135608 | ARHGAP26 | chr5:g.143225373A>G |
NM_015071 | ARHGAP26 | chr5:g.143225373A>G |
NM_001135608 | ARHGAP26 | chr5:g.143225463C>A |
NM_015071 | ARHGAP26 | chr5:g.143225463C>A |
NM_015071 | ARHGAP26 | chr5:g.143227406T>C |
NM_001135608 | ARHGAP26 | chr5:g.143227406T>C |
NM_015071 | ARHGAP26 | chr5:g.143226736C>A |
NM_001135608 | ARHGAP26 | chr5:g.143226736C>A |
NM_015071 | ARHGAP26 | chr5:g.143225607T>C |
NM_001135608 | ARHGAP26 | chr5:g.143225607T>C |
NM_015071 | ARHGAP26 | chr5:g.143224119T>G |
NM_001135608 | ARHGAP26 | chr5:g.143224119T>G |
NM_015071 | ARHGAP26 | chr5:g.143226004C>T |
NM_001135608 | ARHGAP26 | chr5:g.143226004C>T |
NM_015071 | ARHGAP26 | chr5:g.143224856A>G |
NM_001135608 | ARHGAP26 | chr5:g.143224856A>G |
NM_015071 | ARHGAP26 | chr5:g.143227671G>C |
NM_001135608 | ARHGAP26 | chr5:g.143227671G>C |
NM_015071 | ARHGAP26 | chr5:g.143222460C>T |
NM_001135608 | ARHGAP26 | chr5:g.143222460C>T |
NM_015071 | ARHGAP26 | chr5:g.143228381C>T |
NM_001135608 | ARHGAP26 | chr5:g.143228381C>T |
NM_015071 | ARHGAP26 | chr5:g.143225059C>T |
NM_001135608 | ARHGAP26 | chr5:g.143225059C>T |
NM_015071 | ARHGAP26 | chr5:g.143226181C>T |
NM_001135608 | ARHGAP26 | chr5:g.143226181C>T |
NM_015071 | ARHGAP26 | chr5:g.143225612C>T |
NM_001135608 | ARHGAP26 | chr5:g.143225612C>T |
NM_015071 | ARHGAP26 | chr5:g.143227873T>C |
NM_001135608 | ARHGAP26 | chr5:g.143227873T>C |
NM_015071 | ARHGAP26 | chr5:g.143224468G>C |
NM_001135608 | ARHGAP26 | chr5:g.143224468G>C |