SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions |
||||||||
Home | Search | Help | Download |
Browse genes associated with cancer risk that contain miRNA related somatic mutations |
---|
Somatic mutations that alter miRNA target sites: CLASH [1 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001144918 | FGFR2 | chr10:g.121478893C>T |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [2 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001144918 | FGFR2 | chr10:g.121479183G>T |
hsa_circ_0020233 | FGFR2 | chr10:g.121498556G>T |
Somatic mutations that alter predicted mRNA-miRNA target sites [43 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_000141 | FGFR2 | chr10:g.121478674A>T |
NM_001144914 | FGFR2 | chr10:g.121478674A>T |
NM_001144915 | FGFR2 | chr10:g.121478674A>T |
NM_001144916 | FGFR2 | chr10:g.121478674A>T |
NM_001144917 | FGFR2 | chr10:g.121478674A>T |
NM_001144918 | FGFR2 | chr10:g.121478674A>T |
NM_022970 | FGFR2 | chr10:g.121478674A>T |
NM_000141 | FGFR2 | chr10:g.121479598C>T |
NM_001144914 | FGFR2 | chr10:g.121479598C>T |
NM_001144916 | FGFR2 | chr10:g.121479598C>T |
NM_001144917 | FGFR2 | chr10:g.121479598C>T |
NM_001144918 | FGFR2 | chr10:g.121479598C>T |
NM_022970 | FGFR2 | chr10:g.121479598C>T |
NM_001144913 | FGFR2 | chr10:g.121482015G>A |
NM_001144919 | FGFR2 | chr10:g.121482015G>A |
NM_001144916 | FGFR2 | chr10:g.121478481G>A |
NM_001144915 | FGFR2 | chr10:g.121478481G>A |
NM_001144914 | FGFR2 | chr10:g.121478481G>A |
NM_000141 | FGFR2 | chr10:g.121478481G>A |
NM_022970 | FGFR2 | chr10:g.121478481G>A |
NM_001144918 | FGFR2 | chr10:g.121478481G>A |
NM_001144917 | FGFR2 | chr10:g.121478481G>A |
NM_001144915 | FGFR2 | chr10:g.121479183G>T |
NM_001144914 | FGFR2 | chr10:g.121479183G>T |
NM_000141 | FGFR2 | chr10:g.121479183G>T |
NM_022970 | FGFR2 | chr10:g.121479183G>T |
NM_001144918 | FGFR2 | chr10:g.121479183G>T |
NM_001144917 | FGFR2 | chr10:g.121479183G>T |
NM_001144916 | FGFR2 | chr10:g.121479183G>T |
NM_001144916 | FGFR2 | chr10:g.121478893C>T |
NM_001144915 | FGFR2 | chr10:g.121478893C>T |
NM_001144914 | FGFR2 | chr10:g.121478893C>T |
NM_000141 | FGFR2 | chr10:g.121478893C>T |
NM_022970 | FGFR2 | chr10:g.121478893C>T |
NM_001144918 | FGFR2 | chr10:g.121478893C>T |
NM_001144917 | FGFR2 | chr10:g.121478893C>T |
NM_001144916 | FGFR2 | chr10:g.121479070G>T |
NM_001144915 | FGFR2 | chr10:g.121479070G>T |
NM_001144914 | FGFR2 | chr10:g.121479070G>T |
NM_000141 | FGFR2 | chr10:g.121479070G>T |
NM_022970 | FGFR2 | chr10:g.121479070G>T |
NM_001144918 | FGFR2 | chr10:g.121479070G>T |
NM_001144917 | FGFR2 | chr10:g.121479070G>T |