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 [9 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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NM_000318 | PEX2 | chr8:g.76980522T>C |
NM_000318 | PEX2 | chr8:g.76981498A>T |
NM_000318 | PEX2 | chr8:g.76983032A>G |
NM_000318 | PEX2 | chr8:g.76983544A>G |
NM_000318 | PEX2 | chr8:g.76983546C>T |
NM_000318 | PEX2 | chr8:g.76983558C>T |
NM_000318 | PEX2 | chr8:g.76983637A>G |
NM_000318 | PEX2 | chr8:g.76984111T>C |
NM_000318 | PEX2 | chr8:g.76984118G>A |
Somatic mutations that alter predicted mRNA-miRNA target sites [52 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_001079867 | PEX2 | chr8:g.76982407G>A |
NM_000318 | PEX2 | chr8:g.76981223T>G |
NM_001079867 | PEX2 | chr8:g.76981223T>G |
NM_001172086 | PEX2 | chr8:g.76981223T>G |
NM_001172087 | PEX2 | chr8:g.76981223T>G |
NM_000318 | PEX2 | chr8:g.76982744G>C |
NM_001079867 | PEX2 | chr8:g.76982744G>C |
NM_001172086 | PEX2 | chr8:g.76982744G>C |
NM_001172087 | PEX2 | chr8:g.76982744G>C |
NM_000318 | PEX2 | chr8:g.76982407G>A |
NM_001172086 | PEX2 | chr8:g.76982407G>A |
NM_001172087 | PEX2 | chr8:g.76982407G>A |
NM_001172087 | PEX2 | chr8:g.76980581A>C |
NM_001172086 | PEX2 | chr8:g.76980581A>C |
NM_001079867 | PEX2 | chr8:g.76980581A>C |
NM_000318 | PEX2 | chr8:g.76980581A>C |
NM_001172087 | PEX2 | chr8:g.76980522T>C |
NM_001172086 | PEX2 | chr8:g.76980522T>C |
NM_001079867 | PEX2 | chr8:g.76980522T>C |
NM_000318 | PEX2 | chr8:g.76980522T>C |
NM_001172087 | PEX2 | chr8:g.76983032A>G |
NM_001172086 | PEX2 | chr8:g.76983032A>G |
NM_001079867 | PEX2 | chr8:g.76983032A>G |
NM_000318 | PEX2 | chr8:g.76983032A>G |
NM_001172087 | PEX2 | chr8:g.76981498A>T |
NM_001172086 | PEX2 | chr8:g.76981498A>T |
NM_001079867 | PEX2 | chr8:g.76981498A>T |
NM_000318 | PEX2 | chr8:g.76981498A>T |
NM_001172087 | PEX2 | chr8:g.76982549G>A |
NM_001172086 | PEX2 | chr8:g.76982549G>A |
NM_001079867 | PEX2 | chr8:g.76982549G>A |
NM_000318 | PEX2 | chr8:g.76982549G>A |
NM_001172087 | PEX2 | chr8:g.76981659A>G |
NM_001172086 | PEX2 | chr8:g.76981659A>G |
NM_001079867 | PEX2 | chr8:g.76981659A>G |
NM_000318 | PEX2 | chr8:g.76981659A>G |
NM_001172087 | PEX2 | chr8:g.76980383A>T |
NM_001172086 | PEX2 | chr8:g.76980383A>T |
NM_001079867 | PEX2 | chr8:g.76980383A>T |
NM_000318 | PEX2 | chr8:g.76980383A>T |
NM_001172087 | PEX2 | chr8:g.76982447G>A |
NM_001172086 | PEX2 | chr8:g.76982447G>A |
NM_001079867 | PEX2 | chr8:g.76982447G>A |
NM_000318 | PEX2 | chr8:g.76982447G>A |
NM_001172087 | PEX2 | chr8:g.76982943G>C |
NM_001172086 | PEX2 | chr8:g.76982943G>C |
NM_001079867 | PEX2 | chr8:g.76982943G>C |
NM_000318 | PEX2 | chr8:g.76982943G>C |
NM_001172087 | PEX2 | chr8:g.76981874G>A |
NM_001172086 | PEX2 | chr8:g.76981874G>A |
NM_001079867 | PEX2 | chr8:g.76981874G>A |
NM_000318 | PEX2 | chr8:g.76981874G>A |