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: CLASH [3 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001292035 TAB2 chr6:g.149378592C>A
NM_001292035 TAB2 chr6:g.149378817C>T
NM_001292035 TAB2 chr6:g.149378827A>G



Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [79 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001292035 TAB2 chr6:g.149335952A>G
hsa_circ_0078198 TAB2 chr6:g.149359597A>T
hsa_circ_0078198 TAB2 chr6:g.149366906T>A
hsa_circ_0078200 TAB2 chr6:g.149370047G>A
hsa_circ_0078200 TAB2 chr6:g.149370057C>T
hsa_circ_0078200 TAB2 chr6:g.149370058C>T
hsa_circ_0078200 TAB2 chr6:g.149370059C>G
hsa_circ_0078200 TAB2 chr6:g.149370064G>A
hsa_circ_0078200 TAB2 chr6:g.149370070G>A
hsa_circ_0078200 TAB2 chr6:g.149378084G>A
hsa_circ_0078200 TAB2 chr6:g.149378105G>C
hsa_circ_0078200 TAB2 chr6:g.149378114G>T
hsa_circ_0078200 TAB2 chr6:g.149378135C>T
hsa_circ_0078200 TAB2 chr6:g.149378222C>CN
hsa_circ_0078200 TAB2 chr6:g.149378269T>C
hsa_circ_0078200 TAB2 chr6:g.149378275A>G
hsa_circ_0078200 TAB2 chr6:g.149378430C>T
hsa_circ_0078200 TAB2 chr6:g.149378433G>C
hsa_circ_0078200 TAB2 chr6:g.149378473G>T
hsa_circ_0078200 TAB2 chr6:g.149378477G>T
hsa_circ_0078200 TAB2 chr6:g.149378480C>T
hsa_circ_0078200 TAB2 chr6:g.149378523C>T
hsa_circ_0078200 TAB2 chr6:g.149378526T>A
hsa_circ_0078200 TAB2 chr6:g.149378539A>T
hsa_circ_0078200 TAB2 chr6:g.149378542G>T
hsa_circ_0078200 TAB2 chr6:g.149378576A>C
hsa_circ_0078200 TAB2 chr6:g.149378592C>A
hsa_circ_0078200 TAB2 chr6:g.149378660C>T
hsa_circ_0078200 TAB2 chr6:g.149378661A>G
hsa_circ_0078200 TAB2 chr6:g.149378670A>T
hsa_circ_0078200 TAB2 chr6:g.149378694C>T
hsa_circ_0078200 TAB2 chr6:g.149378817C>T
hsa_circ_0078200 TAB2 chr6:g.149378827A>G
hsa_circ_0078200 TAB2 chr6:g.149378837G>T
hsa_circ_0078200 TAB2 chr6:g.149378840C>G
hsa_circ_0078200 TAB2 chr6:g.149378843A>G
hsa_circ_0078200 TAB2 chr6:g.149378850A>G
hsa_circ_0078200 TAB2 chr6:g.149378874G>T
hsa_circ_0078200 TAB2 chr6:g.149378904T>G
hsa_circ_0078200 TAB2 chr6:g.149378919G>C
hsa_circ_0078200 TAB2 chr6:g.149378928C>A
hsa_circ_0078200 TAB2 chr6:g.149378939C>T
hsa_circ_0078200 TAB2 chr6:g.149378982A>G
hsa_circ_0078200 TAB2 chr6:g.149379017T>C
hsa_circ_0078200 TAB2 chr6:g.149379042C>T
hsa_circ_0078200 TAB2 chr6:g.149379102G>C
hsa_circ_0078200 TAB2 chr6:g.149379120G>A
hsa_circ_0078200 TAB2 chr6:g.149379121G>C
hsa_circ_0078200 TAB2 chr6:g.149379131A>G
hsa_circ_0078200 TAB2 chr6:g.149379133A>G
hsa_circ_0078200 TAB2 chr6:g.149379156G>C
hsa_circ_0078200 TAB2 chr6:g.149379233A>G
hsa_circ_0078200 TAB2 chr6:g.149379240C>T
hsa_circ_0078200 TAB2 chr6:g.149379266C>T
hsa_circ_0078200 TAB2 chr6:g.149379267C>A
hsa_circ_0078200 TAB2 chr6:g.149379269C>T
hsa_circ_0078200 TAB2 chr6:g.149379295G>A
hsa_circ_0078200 TAB2 chr6:g.149379303C>T
hsa_circ_0078200 TAB2 chr6:g.149379319C>A
hsa_circ_0078200 TAB2 chr6:g.149379333C>T
hsa_circ_0078200 TAB2 chr6:g.149379346A>G
hsa_circ_0078200 TAB2 chr6:g.149379355G>A
hsa_circ_0078200 TAB2 chr6:g.149379367C>T
hsa_circ_0078200 TAB2 chr6:g.149379392C>T
hsa_circ_0078200 TAB2 chr6:g.149379435C>T
hsa_circ_0078200 TAB2 chr6:g.149379491G>T
hsa_circ_0078200 TAB2 chr6:g.149379493A>T
hsa_circ_0078200 TAB2 chr6:g.149379501A>T
hsa_circ_0078200 TAB2 chr6:g.149379511C>A
NM_001292035 TAB2 chr6:g.149397602A>G
NM_001292035 TAB2 chr6:g.149397606C>T
NM_001292035 TAB2 chr6:g.149397628G>C
NM_001292035 TAB2 chr6:g.149397739C>G
NM_001292035 TAB2 chr6:g.149399111T>C
NM_001292035 TAB2 chr6:g.149399160G>A
NM_001292035 TAB2 chr6:g.149399164C>T
NM_001292035 TAB2 chr6:g.149400394G>A
NM_001292035 TAB2 chr6:g.149410601A>T
NM_001292035 TAB2 chr6:g.149410610A>G



Somatic mutations that alter predicted mRNA-miRNA target sites [5 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_015093 TAB2 chr6:g.149410340C>G
NM_015093 TAB2 chr6:g.149410601A>T
NM_015093 TAB2 chr6:g.149410610A>G
NM_015093 TAB2 chr6:g.149410888T>-
NM_015093 TAB2 chr6:g.149410903G>A