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: PAR-CLIP and HITS-CLIP [29 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_021005 | NR2F2 | chr15:g.96331849G>A |
NM_021005 | NR2F2 | chr15:g.96337821TAA>T |
NM_021005 | NR2F2 | chr15:g.96337987C>CT |
NM_021005 | NR2F2 | chr15:g.96338175A>G |
NM_021005 | NR2F2 | chr15:g.96338582G>T |
NM_021005 | NR2F2 | chr15:g.96332380G>A |
hsa_circ_0037018 | NR2F2 | chr15:g.96334148T>C |
hsa_circ_0037018 | NR2F2 | chr15:g.96334149C>G |
hsa_circ_0037018 | NR2F2 | chr15:g.96334150A>T |
hsa_circ_0037018 | NR2F2 | chr15:g.96334174T>C |
hsa_circ_0037018 | NR2F2 | chr15:g.96334177A>C |
hsa_circ_0037018 | NR2F2 | chr15:g.96334184T>C |
hsa_circ_0037018 | NR2F2 | chr15:g.96334192C>T |
hsa_circ_0037018 | NR2F2 | chr15:g.96334324C>T |
hsa_circ_0037018 | NR2F2 | chr15:g.96334332C>T |
hsa_circ_0037018 | NR2F2 | chr15:g.96334333C>T |
hsa_circ_0037018 | NR2F2 | chr15:g.96334334C>G |
hsa_circ_0037018 | NR2F2 | chr15:g.96334510C>T |
NM_021005 | NR2F2 | chr15:g.96337392GAA>G |
NM_021005 | NR2F2 | chr15:g.96337453G>C |
NM_021005 | NR2F2 | chr15:g.96337471T>C |
NM_021005 | NR2F2 | chr15:g.96337473C>T |
NM_021005 | NR2F2 | chr15:g.96337479C>A |
NM_021005 | NR2F2 | chr15:g.96337494G>A |
NM_021005 | NR2F2 | chr15:g.96337506G>T |
NM_021005 | NR2F2 | chr15:g.96337527G>T |
NM_021005 | NR2F2 | chr15:g.96337540G>A |
NM_021005 | NR2F2 | chr15:g.96337617C>T |
NM_021005 | NR2F2 | chr15:g.96337622A>C |
Somatic mutations that alter predicted mRNA-miRNA target sites [32 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001145155 | NR2F2 | chr15:g.96339808A>C |
NM_001145156 | NR2F2 | chr15:g.96339808A>C |
NM_001145157 | NR2F2 | chr15:g.96339808A>C |
NM_021005 | NR2F2 | chr15:g.96339808A>C |
NM_021005 | NR2F2 | chr15:g.96337988->T |
NM_001145157 | NR2F2 | chr15:g.96337988->T |
NM_001145156 | NR2F2 | chr15:g.96337988->T |
NM_001145155 | NR2F2 | chr15:g.96337988->T |
NM_021005 | NR2F2 | chr15:g.96337957G>A |
NM_001145157 | NR2F2 | chr15:g.96337957G>A |
NM_001145156 | NR2F2 | chr15:g.96337957G>A |
NM_001145155 | NR2F2 | chr15:g.96337957G>A |
NM_021005 | NR2F2 | chr15:g.96338898G>T |
NM_001145157 | NR2F2 | chr15:g.96338898G>T |
NM_001145156 | NR2F2 | chr15:g.96338898G>T |
NM_001145155 | NR2F2 | chr15:g.96338898G>T |
NM_021005 | NR2F2 | chr15:g.96338582G>T |
NM_001145157 | NR2F2 | chr15:g.96338582G>T |
NM_001145156 | NR2F2 | chr15:g.96338582G>T |
NM_001145155 | NR2F2 | chr15:g.96338582G>T |
NM_021005 | NR2F2 | chr15:g.96338175A>G |
NM_001145157 | NR2F2 | chr15:g.96338175A>G |
NM_001145156 | NR2F2 | chr15:g.96338175A>G |
NM_001145155 | NR2F2 | chr15:g.96338175A>G |
NM_021005 | NR2F2 | chr15:g.96339386A>T |
NM_001145157 | NR2F2 | chr15:g.96339386A>T |
NM_001145156 | NR2F2 | chr15:g.96339386A>T |
NM_001145155 | NR2F2 | chr15:g.96339386A>T |
NM_021005 | NR2F2 | chr15:g.96339930T>A |
NM_001145157 | NR2F2 | chr15:g.96339930T>A |
NM_001145156 | NR2F2 | chr15:g.96339930T>A |
NM_001145155 | NR2F2 | chr15:g.96339930T>A |