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 |
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Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [1 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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hsa_circ_0083896 | NRG1 | chr8:g.32693080A>G |
Somatic mutations that alter predicted mRNA-miRNA target sites [66 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_013962 | NRG1 | chr8:g.32743123G>A |
NM_013959 | NRG1 | chr8:g.32743123G>A |
NM_013958 | NRG1 | chr8:g.32743123G>A |
NM_001160005 | NRG1 | chr8:g.32743123G>A |
NM_001159996 | NRG1 | chr8:g.32764103G>A |
NM_001160004 | NRG1 | chr8:g.32764103G>A |
NM_013960 | NRG1 | chr8:g.32764103G>A |
NM_001159996 | NRG1 | chr8:g.32763880G>A |
NM_001160004 | NRG1 | chr8:g.32763880G>A |
NM_013960 | NRG1 | chr8:g.32763880G>A |
NM_001159996 | NRG1 | chr8:g.32764099A>G |
NM_001160004 | NRG1 | chr8:g.32764099A>G |
NM_013960 | NRG1 | chr8:g.32764099A>G |
NM_001159996 | NRG1 | chr8:g.32763997G>A |
NM_001160004 | NRG1 | chr8:g.32763997G>A |
NM_013960 | NRG1 | chr8:g.32763997G>A |
NM_001159996 | NRG1 | chr8:g.32763938C>T |
NM_001160004 | NRG1 | chr8:g.32763938C>T |
NM_013960 | NRG1 | chr8:g.32763938C>T |
NM_001159996 | NRG1 | chr8:g.32763918T>G |
NM_001160004 | NRG1 | chr8:g.32763918T>G |
NM_013960 | NRG1 | chr8:g.32763918T>G |
NM_001160008 | NRG1 | chr8:g.32760871C>A |
NM_001160005 | NRG1 | chr8:g.32743224G>T |
NM_013958 | NRG1 | chr8:g.32743224G>T |
NM_013959 | NRG1 | chr8:g.32743224G>T |
NM_013962 | NRG1 | chr8:g.32743224G>T |
NM_001159996 | NRG1 | chr8:g.32764346G>A |
NM_001160004 | NRG1 | chr8:g.32764346G>A |
NM_013960 | NRG1 | chr8:g.32764346G>A |
NM_001159996 | NRG1 | chr8:g.32763920G>A |
NM_001160004 | NRG1 | chr8:g.32763920G>A |
NM_013960 | NRG1 | chr8:g.32763920G>A |
NM_001159996 | NRG1 | chr8:g.32764430G>A |
NM_001160004 | NRG1 | chr8:g.32764430G>A |
NM_013960 | NRG1 | chr8:g.32764430G>A |
NM_001159996 | NRG1 | chr8:g.32764064A>A |
NM_001160004 | NRG1 | chr8:g.32764064A>A |
NM_013960 | NRG1 | chr8:g.32764064A>A |
NM_001159996 | NRG1 | chr8:g.32763930C>A |
NM_001160004 | NRG1 | chr8:g.32763930C>A |
NM_013960 | NRG1 | chr8:g.32763930C>A |
NM_001159996 | NRG1 | chr8:g.32764125G>T |
NM_001160004 | NRG1 | chr8:g.32764125G>T |
NM_013960 | NRG1 | chr8:g.32764125G>T |
NM_001159995 | NRG1 | chr8:g.32764430G>A |
NM_001159999 | NRG1 | chr8:g.32764430G>A |
NM_001160001 | NRG1 | chr8:g.32764430G>A |
NM_013956 | NRG1 | chr8:g.32764430G>A |
NM_013957 | NRG1 | chr8:g.32764430G>A |
NM_013964 | NRG1 | chr8:g.32764430G>A |
NM_013962 | NRG1 | chr8:g.32742888A>C |
NM_013959 | NRG1 | chr8:g.32742888A>C |
NM_013958 | NRG1 | chr8:g.32742888A>C |
NM_001160005 | NRG1 | chr8:g.32742888A>C |
NM_004495 | NRG1 | chr8:g.32728546C>T |
NM_001160007 | NRG1 | chr8:g.32728546C>T |
NM_001160002 | NRG1 | chr8:g.32728546C>T |
NM_001159999 | NRG1 | chr8:g.32764962A>G |
NM_013964 | NRG1 | chr8:g.32764962A>G |
NM_001159995 | NRG1 | chr8:g.32764962A>G |
NM_001160001 | NRG1 | chr8:g.32764962A>G |
NM_013956 | NRG1 | chr8:g.32764962A>G |
NM_013957 | NRG1 | chr8:g.32764962A>G |
NM_001160008 | NRG1 | chr8:g.32760653G>A |
NM_001160008 | NRG1 | chr8:g.32760486G>A |