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 [53 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_001024847 TGFBR2 chr3:g.30691800A>G
NM_001024847 TGFBR2 chr3:g.30692281A>T
NM_001024847 TGFBR2 chr3:g.30693226C>T
NM_001024847 TGFBR2 chr3:g.30693899C>T
hsa_circ_0064654 TGFBR2 chr3:g.30644819T>C
hsa_circ_0064655 TGFBR2 chr3:g.30650283G>A
hsa_circ_0064655 TGFBR2 chr3:g.30650289A>T
hsa_circ_0064655 TGFBR2 chr3:g.30650291A>G
hsa_circ_0064655 TGFBR2 chr3:g.30650296T>G
hsa_circ_0064655 TGFBR2 chr3:g.30650309C>T
hsa_circ_0064655 TGFBR2 chr3:g.30650313G>A
hsa_circ_0064655 TGFBR2 chr3:g.30650314A>G
hsa_circ_0064655 TGFBR2 chr3:g.30650320A>T
hsa_circ_0064655 TGFBR2 chr3:g.30650321G>A
hsa_circ_0064655 TGFBR2 chr3:g.30650406T>G
hsa_circ_0064655 TGFBR2 chr3:g.30671685A>G
hsa_circ_0064655 TGFBR2 chr3:g.30672098C>T
hsa_circ_0064655 TGFBR2 chr3:g.30672099C>T
hsa_circ_0064655 TGFBR2 chr3:g.30674168G>T
hsa_circ_0064655 TGFBR2 chr3:g.30674171T>C
hsa_circ_0064655 TGFBR2 chr3:g.30674172C>T
hsa_circ_0064655 TGFBR2 chr3:g.30674175T>C
hsa_circ_0064655 TGFBR2 chr3:g.30674186G>A
hsa_circ_0064655 TGFBR2 chr3:g.30674187A>T
hsa_circ_0064655 TGFBR2 chr3:g.30674193A>G
hsa_circ_0064655 TGFBR2 chr3:g.30674205T>C
hsa_circ_0064655 TGFBR2 chr3:g.30674206G>A
hsa_circ_0064655 TGFBR2 chr3:g.30674211T>C
hsa_circ_0064655 TGFBR2 chr3:g.30674214G>C
hsa_circ_0064655 TGFBR2 chr3:g.30674223C>A
hsa_circ_0064655 TGFBR2 chr3:g.30674229G>T
NM_001024847 TGFBR2 chr3:g.30688395T>G
NM_001024847 TGFBR2 chr3:g.30688421G>A
NM_001024847 TGFBR2 chr3:g.30688422C>T
NM_001024847 TGFBR2 chr3:g.30688423G>A
NM_001024847 TGFBR2 chr3:g.30688425G>T
NM_001024847 TGFBR2 chr3:g.30691435T>C
NM_001024847 TGFBR2 chr3:g.30691447A>T
NM_001024847 TGFBR2 chr3:g.30691449T>C
NM_001024847 TGFBR2 chr3:g.30691449T>A
NM_001024847 TGFBR2 chr3:g.30691450G>A
NM_001024847 TGFBR2 chr3:g.30691456T>C
NM_001024847 TGFBR2 chr3:g.30691457G>A
NM_001024847 TGFBR2 chr3:g.30691458G>A
NM_001024847 TGFBR2 chr3:g.30691458G>T
NM_001024847 TGFBR2 chr3:g.30691464C>T
NM_001024847 TGFBR2 chr3:g.30691465G>T
NM_001024847 TGFBR2 chr3:g.30691465G>A
NM_001024847 TGFBR2 chr3:g.30691466A>G
NM_001024847 TGFBR2 chr3:g.30691468C>T
NM_001024847 TGFBR2 chr3:g.30691469C>A
NM_001024847 TGFBR2 chr3:g.30691471G>A
NM_001024847 TGFBR2 chr3:g.30691580C>T



Somatic mutations that alter predicted mRNA-miRNA target sites [14 records found]

[download data table]
Transcript ID Gene Symbol Mutation ID
NM_003242 TGFBR2 chr3:g.30692281A>T
NM_001024847 TGFBR2 chr3:g.30692281A>T
NM_003242 TGFBR2 chr3:g.30691800A>G
NM_001024847 TGFBR2 chr3:g.30691800A>G
NM_003242 TGFBR2 chr3:g.30693899C>T
NM_001024847 TGFBR2 chr3:g.30693899C>T
NM_003242 TGFBR2 chr3:g.30693871G>T
NM_001024847 TGFBR2 chr3:g.30693871G>T
NM_003242 TGFBR2 chr3:g.30693399G>C
NM_001024847 TGFBR2 chr3:g.30693399G>C
NM_003242 TGFBR2 chr3:g.30693226C>T
NM_001024847 TGFBR2 chr3:g.30693226C>T
NM_003242 TGFBR2 chr3:g.30693615G>C
NM_001024847 TGFBR2 chr3:g.30693615G>C