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 [135 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001040092 ENPP2 chr8:g.119557528A>G
NM_001040092 ENPP2 chr8:g.119557530C>T
NM_001040092 ENPP2 chr8:g.119557545G>A
NM_001040092 ENPP2 chr8:g.119557569A>C
NM_001040092 ENPP2 chr8:g.119557574C>T
NM_001040092 ENPP2 chr8:g.119557590G>A
NM_001040092 ENPP2 chr8:g.119557590G>C
NM_001040092 ENPP2 chr8:g.119557594G>A
NM_001040092 ENPP2 chr8:g.119557635G>A
NM_001040092 ENPP2 chr8:g.119557637A>C
NM_001040092 ENPP2 chr8:g.119557653G>A
NM_001040092 ENPP2 chr8:g.119557654T>C
NM_001040092 ENPP2 chr8:g.119557664G>A
NM_001040092 ENPP2 chr8:g.119557680C>T
NM_001040092 ENPP2 chr8:g.119562871G>T
NM_001040092 ENPP2 chr8:g.119562872C>A
NM_001040092 ENPP2 chr8:g.119562872C>T
NM_001040092 ENPP2 chr8:g.119562874A>G
NM_001040092 ENPP2 chr8:g.119562896C>T
NM_001040092 ENPP2 chr8:g.119562909C>G
NM_001040092 ENPP2 chr8:g.119562911C>G
NM_001040092 ENPP2 chr8:g.119562914T>C
NM_001040092 ENPP2 chr8:g.119562916C>A
NM_001040092 ENPP2 chr8:g.119562918G>T
NM_001040092 ENPP2 chr8:g.119562919G>A
NM_001040092 ENPP2 chr8:g.119562924G>A
NM_001040092 ENPP2 chr8:g.119562931G>A
NM_001040092 ENPP2 chr8:g.119562969G>A
NM_001040092 ENPP2 chr8:g.119562981C>G
NM_001040092 ENPP2 chr8:g.119562990C>A
NM_001040092 ENPP2 chr8:g.119563003G>A
NM_001040092 ENPP2 chr8:g.119564839G>A
NM_001040092 ENPP2 chr8:g.119564861C>T
NM_001040092 ENPP2 chr8:g.119564870C>T
NM_001040092 ENPP2 chr8:g.119564891C>T
NM_001040092 ENPP2 chr8:g.119564895T>G
NM_001040092 ENPP2 chr8:g.119564918A>C
NM_001040092 ENPP2 chr8:g.119564921G>T
NM_001040092 ENPP2 chr8:g.119564932GGG>AAG
NM_001040092 ENPP2 chr8:g.119564943A>G
NM_001040092 ENPP2 chr8:g.119564949G>A
NM_001040092 ENPP2 chr8:g.119570805A>T
NM_001040092 ENPP2 chr8:g.119570814C>T
NM_001040092 ENPP2 chr8:g.119570821C>T
NM_001040092 ENPP2 chr8:g.119570823G>T
NM_001040092 ENPP2 chr8:g.119570828C>G
NM_001040092 ENPP2 chr8:g.119582446G>T
NM_001040092 ENPP2 chr8:g.119582448C>A
NM_001040092 ENPP2 chr8:g.119582471C>A
NM_001040092 ENPP2 chr8:g.119582517C>T
NM_001040092 ENPP2 chr8:g.119582540C>T
NM_001040092 ENPP2 chr8:g.119582548A>G
NM_001040092 ENPP2 chr8:g.119582553G>A
NM_001040092 ENPP2 chr8:g.119582559A>T
NM_001040092 ENPP2 chr8:g.119582562T>C
NM_001040092 ENPP2 chr8:g.119582565C>G
NM_001040092 ENPP2 chr8:g.119582574T>C
NM_001040092 ENPP2 chr8:g.119582579C>G
NM_001040092 ENPP2 chr8:g.119582585C>T
NM_001040092 ENPP2 chr8:g.119583739T>C
NM_001040092 ENPP2 chr8:g.119583774A>G
NM_001040092 ENPP2 chr8:g.119586192T>C
NM_001040092 ENPP2 chr8:g.119586205C>T
NM_001040092 ENPP2 chr8:g.119586221C>G
NM_001040092 ENPP2 chr8:g.119586229G>C
NM_001040092 ENPP2 chr8:g.119586246C>T
NM_001040092 ENPP2 chr8:g.119586251C>G
NM_001040092 ENPP2 chr8:g.119586253C>T
NM_001040092 ENPP2 chr8:g.119586259C>T
NM_001040092 ENPP2 chr8:g.119586263C>G
NM_001040092 ENPP2 chr8:g.119586292T>A
NM_001040092 ENPP2 chr8:g.119586304C>A
NM_001040092 ENPP2 chr8:g.119590528C>A
NM_001040092 ENPP2 chr8:g.119590528C>T
NM_001040092 ENPP2 chr8:g.119590532C>T
NM_001040092 ENPP2 chr8:g.119590537G>T
NM_001040092 ENPP2 chr8:g.119590544C>G
NM_001040092 ENPP2 chr8:g.119590562A>G
NM_001040092 ENPP2 chr8:g.119590568G>T
hsa_circ_0085387 ENPP2 chr8:g.119600680G>A
hsa_circ_0085387 ENPP2 chr8:g.119600682C>A
hsa_circ_0085387 ENPP2 chr8:g.119600687C>T
hsa_circ_0085387 ENPP2 chr8:g.119600692C>A
hsa_circ_0085387 ENPP2 chr8:g.119600711C>A
hsa_circ_0085387 ENPP2 chr8:g.119600742T>C
hsa_circ_0085387 ENPP2 chr8:g.119600745C>T
NM_001040092 ENPP2 chr8:g.119607960C>T
NM_001040092 ENPP2 chr8:g.119607975A>G
NM_001040092 ENPP2 chr8:g.119616265G>A
NM_001040092 ENPP2 chr8:g.119616265G>T
NM_001040092 ENPP2 chr8:g.119616266C>T
NM_001040092 ENPP2 chr8:g.119616268A>T
NM_001040092 ENPP2 chr8:g.119616276G>A
NM_001040092 ENPP2 chr8:g.119616298G>A
NM_001040092 ENPP2 chr8:g.119616309C>T
NM_001040092 ENPP2 chr8:g.119616311T>A
NM_001040092 ENPP2 chr8:g.119616314A>G
NM_001040092 ENPP2 chr8:g.119616319T>G
NM_001040092 ENPP2 chr8:g.119616353G>T
NM_001040092 ENPP2 chr8:g.119617481A>G
NM_001040092 ENPP2 chr8:g.119617502A>T
NM_001040092 ENPP2 chr8:g.119617506G>T
NM_001040092 ENPP2 chr8:g.119617519G>A
NM_001040092 ENPP2 chr8:g.119617536C>A
NM_001040092 ENPP2 chr8:g.119621421T>A
NM_001040092 ENPP2 chr8:g.119621435C>G
NM_001040092 ENPP2 chr8:g.119621459G>A
NM_001040092 ENPP2 chr8:g.119621463G>T
NM_001040092 ENPP2 chr8:g.119621466A>C
NM_001040092 ENPP2 chr8:g.119621469G>T
NM_001040092 ENPP2 chr8:g.119621484G>A
NM_001040092 ENPP2 chr8:g.119621484G>T
NM_001040092 ENPP2 chr8:g.119621509G>A
NM_001040092 ENPP2 chr8:g.119621510G>T
NM_001040092 ENPP2 chr8:g.119621518C>A
NM_001040092 ENPP2 chr8:g.119626572G>A
NM_001040092 ENPP2 chr8:g.119626574T>G
NM_001040092 ENPP2 chr8:g.119626580C>A
NM_001040092 ENPP2 chr8:g.119626615A>TA
NM_001040092 ENPP2 chr8:g.119626617T>G
NM_001040092 ENPP2 chr8:g.119626680C>A
NM_001040092 ENPP2 chr8:g.119626701G>T
NM_001040092 ENPP2 chr8:g.119626705C>T
NM_001040092 ENPP2 chr8:g.119638425G>A
NM_001040092 ENPP2 chr8:g.119638434C>T
NM_001040092 ENPP2 chr8:g.119638441G>A
NM_001040092 ENPP2 chr8:g.119638448G>A
NM_001040092 ENPP2 chr8:g.119638466G>A
NM_001040092 ENPP2 chr8:g.119638479T>A
NM_001040092 ENPP2 chr8:g.119638492T>C
NM_001040092 ENPP2 chr8:g.119638499G>A
NM_001040092 ENPP2 chr8:g.119638503G>A
NM_001040092 ENPP2 chr8:g.119638513C>A
NM_001040092 ENPP2 chr8:g.119638520C>T
NM_001040092 ENPP2 chr8:g.119638764C>T



Somatic mutations that alter predicted mRNA-miRNA target sites [1 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001130863 ENPP2 chr8:g.119557511C>A