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


Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [74 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001042599 ERBB4 chr2:g.211375857C>T
NM_001042599 ERBB4 chr2:g.211376177C>T
NM_001042599 ERBB4 chr2:g.211376975T>G
NM_001042599 ERBB4 chr2:g.211377002A>C
NM_001042599 ERBB4 chr2:g.211377355A>G
NM_001042599 ERBB4 chr2:g.211382200A>T
NM_001042599 ERBB4 chr2:g.211383535T>G
NM_001042599 ERBB4 chr2:g.211776104T>A
NM_001042599 ERBB4 chr2:g.211807105C>A
NM_001042599 ERBB4 chr2:g.211900407A>C
NM_001042599 ERBB4 chr2:g.211939045G>A
NM_001042599 ERBB4 chr2:g.212055385T>A
NM_001042599 ERBB4 chr2:g.212213710C>A
NM_001042599 ERBB4 chr2:g.212277125T>C
NM_001042599 ERBB4 chr2:g.212283427A>G
NM_001042599 ERBB4 chr2:g.212283447A>G
NM_001042599 ERBB4 chr2:g.212290296C>T
NM_001042599 ERBB4 chr2:g.212295875T>C
NM_001042599 ERBB4 chr2:g.212307656T>C
NM_001042599 ERBB4 chr2:g.212307670T>C
NM_001042599 ERBB4 chr2:g.212319891G>A
NM_001042599 ERBB4 chr2:g.212363511G>T
NM_001042599 ERBB4 chr2:g.212435934A>G
NM_001042599 ERBB4 chr2:g.212437327G>C
NM_001042599 ERBB4 chr2:g.212437382A>T
NM_001042599 ERBB4 chr2:g.212460239T>C
NM_001042599 ERBB4 chr2:g.212486287C>T
NM_001042599 ERBB4 chr2:g.212494870A>G
NM_001042599 ERBB4 chr2:g.211383695G>C
NM_001042599 ERBB4 chr2:g.211383698C>G
NM_001042599 ERBB4 chr2:g.211383705A>T
NM_001042599 ERBB4 chr2:g.211383716C>G
NM_001042599 ERBB4 chr2:g.211383722A>T
NM_001042599 ERBB4 chr2:g.211383724G>A
NM_001042599 ERBB4 chr2:g.211383725C>T
NM_001042599 ERBB4 chr2:g.211383849G>C
NM_001042599 ERBB4 chr2:g.211383851G>A
NM_001042599 ERBB4 chr2:g.211383855G>A
NM_001042599 ERBB4 chr2:g.211384038G>T
NM_001042599 ERBB4 chr2:g.211384044G>A
NM_001042599 ERBB4 chr2:g.211384045T>A
NM_001042599 ERBB4 chr2:g.211384048C>T
NM_001042599 ERBB4 chr2:g.211384054T>C
NM_001042599 ERBB4 chr2:g.211424176G>A
NM_001042599 ERBB4 chr2:g.211424178A>T
NM_001042599 ERBB4 chr2:g.211424181T>C
NM_001042599 ERBB4 chr2:g.211424189C>A
NM_001042599 ERBB4 chr2:g.211424194C>T
NM_001042599 ERBB4 chr2:g.211424197C>T
NM_001042599 ERBB4 chr2:g.211424200C>T
hsa_circ_0058031 ERBB4 chr2:g.211630527G>T
NM_001042599 ERBB4 chr2:g.211665428G>T
NM_001042599 ERBB4 chr2:g.211665431A>G
NM_001042599 ERBB4 chr2:g.211665437G>A
NM_001042599 ERBB4 chr2:g.211665438G>A
NM_001042599 ERBB4 chr2:g.211702005G>A
NM_001042599 ERBB4 chr2:g.211702009C>G
NM_001042599 ERBB4 chr2:g.211702016A>T
NM_001042599 ERBB4 chr2:g.211702024T>G
NM_001042599 ERBB4 chr2:g.211702025C>G
NM_001042599 ERBB4 chr2:g.211702026T>C
NM_001042599 ERBB4 chr2:g.211702033A>C
NM_001042599 ERBB4 chr2:g.211702037C>G
NM_001042599 ERBB4 chr2:g.211704151C>T
NM_001042599 ERBB4 chr2:g.211704160G>A
NM_001042599 ERBB4 chr2:g.211704167C>T
NM_001042599 ERBB4 chr2:g.211713616C>A
NM_001042599 ERBB4 chr2:g.211713616C>T
NM_001042599 ERBB4 chr2:g.211713621G>T
NM_001042599 ERBB4 chr2:g.211713623T>C
NM_001042599 ERBB4 chr2:g.211713624C>A
NM_001042599 ERBB4 chr2:g.211713624C>T
NM_001042599 ERBB4 chr2:g.211713628A>G
NM_001042599 ERBB4 chr2:g.211713638G>A



Somatic mutations that alter predicted mRNA-miRNA target sites [66 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001042599 ERBB4 chr2:g.211377400G>A
NM_005235 ERBB4 chr2:g.211377400G>A
NM_001042599 ERBB4 chr2:g.211381682T>A
NM_005235 ERBB4 chr2:g.211381682T>A
NM_005235 ERBB4 chr2:g.211377355A>G
NM_001042599 ERBB4 chr2:g.211378500C>A
NM_005235 ERBB4 chr2:g.211378500C>A
NM_005235 ERBB4 chr2:g.211377395T>A
NM_005235 ERBB4 chr2:g.211382487G>A
NM_001042599 ERBB4 chr2:g.211378704G>A
NM_005235 ERBB4 chr2:g.211378704G>A
NM_001042599 ERBB4 chr2:g.211382487G>A
NM_001042599 ERBB4 chr2:g.211377395T>A
NM_001042599 ERBB4 chr2:g.211377355A>G
NM_001042599 ERBB4 chr2:g.211381441G>A
NM_005235 ERBB4 chr2:g.211381441G>A
NM_001042599 ERBB4 chr2:g.211381466T>C
NM_005235 ERBB4 chr2:g.211381466T>C
NM_001042599 ERBB4 chr2:g.211377676A>T
NM_005235 ERBB4 chr2:g.211377676A>T
NM_001042599 ERBB4 chr2:g.211379687A>G
NM_005235 ERBB4 chr2:g.211379687A>G
NM_001042599 ERBB4 chr2:g.211375857C>T
NM_005235 ERBB4 chr2:g.211375857C>T
NM_001042599 ERBB4 chr2:g.211376975T>G
NM_005235 ERBB4 chr2:g.211376975T>G
NM_001042599 ERBB4 chr2:g.211380881G>T
NM_005235 ERBB4 chr2:g.211380881G>T
NM_001042599 ERBB4 chr2:g.211375975G>A
NM_005235 ERBB4 chr2:g.211375975G>A
NM_001042599 ERBB4 chr2:g.211379919G>T
NM_005235 ERBB4 chr2:g.211379919G>T
NM_001042599 ERBB4 chr2:g.211381326T>A
NM_005235 ERBB4 chr2:g.211381326T>A
NM_001042599 ERBB4 chr2:g.211379172C>T
NM_005235 ERBB4 chr2:g.211379172C>T
NM_001042599 ERBB4 chr2:g.211377002A>C
NM_005235 ERBB4 chr2:g.211377002A>C
NM_001042599 ERBB4 chr2:g.211376177C>T
NM_005235 ERBB4 chr2:g.211376177C>T
NM_001042599 ERBB4 chr2:g.211382901T>C
NM_005235 ERBB4 chr2:g.211382901T>C
NM_001042599 ERBB4 chr2:g.211377052T>A
NM_005235 ERBB4 chr2:g.211377052T>A
NM_001042599 ERBB4 chr2:g.211377211T>C
NM_005235 ERBB4 chr2:g.211377211T>C
NM_001042599 ERBB4 chr2:g.211381448C>T
NM_005235 ERBB4 chr2:g.211381448C>T
NM_001042599 ERBB4 chr2:g.211376095A>T
NM_005235 ERBB4 chr2:g.211376095A>T
NM_001042599 ERBB4 chr2:g.211377232G>A
NM_005235 ERBB4 chr2:g.211377232G>A
NM_001042599 ERBB4 chr2:g.211378582A>T
NM_005235 ERBB4 chr2:g.211378582A>T
NM_001042599 ERBB4 chr2:g.211376051A>G
NM_005235 ERBB4 chr2:g.211376051A>G
NM_001042599 ERBB4 chr2:g.211376421T>A
NM_005235 ERBB4 chr2:g.211376421T>A
NM_001042599 ERBB4 chr2:g.211382200A>T
NM_005235 ERBB4 chr2:g.211382200A>T
NM_001042599 ERBB4 chr2:g.211380892T>C
NM_005235 ERBB4 chr2:g.211380892T>C
NM_001042599 ERBB4 chr2:g.211378932A>T
NM_005235 ERBB4 chr2:g.211378932A>T
NM_001042599 ERBB4 chr2:g.211379055A>G
NM_005235 ERBB4 chr2:g.211379055A>G