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 [40 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NR_033702 MYNN chr3:g.169774288A>G
NR_033702 MYNN chr3:g.169785773A>G
NR_033702 MYNN chr3:g.169774299C>T
NR_033702 MYNN chr3:g.169774306C>T
NR_033702 MYNN chr3:g.169774313C>T
NR_033702 MYNN chr3:g.169774322C>T
NR_033702 MYNN chr3:g.169774346G>A
NR_033702 MYNN chr3:g.169774364C>T
NR_033702 MYNN chr3:g.169774364C>G
NR_033702 MYNN chr3:g.169778781G>T
NR_033702 MYNN chr3:g.169778807C>G
NR_033702 MYNN chr3:g.169778833G>A
NR_033702 MYNN chr3:g.169778889T>C
NR_033702 MYNN chr3:g.169779064C>A
NR_033702 MYNN chr3:g.169779065C>T
NR_033702 MYNN chr3:g.169779067C>T
NR_033702 MYNN chr3:g.169779147A>G
NR_033702 MYNN chr3:g.169779261G>T
NR_033702 MYNN chr3:g.169779265C>T
NR_033702 MYNN chr3:g.169779269G>A
NR_033702 MYNN chr3:g.169779415A>G
NR_033702 MYNN chr3:g.169780627A>G
NR_033702 MYNN chr3:g.169780645G>A
NR_033702 MYNN chr3:g.169780651C>G
NR_033702 MYNN chr3:g.169780662G>A
NR_033702 MYNN chr3:g.169780704G>T
NR_033702 MYNN chr3:g.169782525C>A
NR_033702 MYNN chr3:g.169782595G>A
NR_033702 MYNN chr3:g.169782609T>C
NR_033702 MYNN chr3:g.169783508G>C
NR_033702 MYNN chr3:g.169783518A>T
NR_033702 MYNN chr3:g.169783522C>T
NR_033702 MYNN chr3:g.169783523C>A
NR_033702 MYNN chr3:g.169783530G>C
hsa_circ_0067879 MYNN chr3:g.169786513G>T
hsa_circ_0067879 MYNN chr3:g.169786526A>G
hsa_circ_0067879 MYNN chr3:g.169786557A>T
hsa_circ_0067879 MYNN chr3:g.169786563A>G
hsa_circ_0067879 MYNN chr3:g.169786655AT>A
hsa_circ_0067879 MYNN chr3:g.169786659T>A



Somatic mutations that alter predicted mRNA-miRNA target sites [12 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001185118 MYNN chr3:g.169789582A>G
NM_001185119 MYNN chr3:g.169789582A>G
NM_018657 MYNN chr3:g.169789582A>G
NM_001185118 MYNN chr3:g.169789622T>G
NM_001185119 MYNN chr3:g.169789622T>G
NM_018657 MYNN chr3:g.169789622T>G
NM_001185118 MYNN chr3:g.169787975T>C
NM_001185119 MYNN chr3:g.169787975T>C
NM_018657 MYNN chr3:g.169787975T>C
NM_001185118 MYNN chr3:g.169788899T>C
NM_001185119 MYNN chr3:g.169788899T>C
NM_018657 MYNN chr3:g.169788899T>C