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: CLASH [1 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
NM_004800 | TM9SF2 | chr13:g.99529487G>T |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [65 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0030736 | TM9SF2 | chr13:g.99562834T>G |
NM_004800 | TM9SF2 | chr13:g.99501656T>C |
NM_004800 | TM9SF2 | chr13:g.99501695C>G |
NM_004800 | TM9SF2 | chr13:g.99501702G>A |
NM_004800 | TM9SF2 | chr13:g.99501735C>T |
NM_004800 | TM9SF2 | chr13:g.99501751G>A |
NM_004800 | TM9SF2 | chr13:g.99501754GA>G |
hsa_circ_0030729 | TM9SF2 | chr13:g.99517623G>T |
hsa_circ_0030729 | TM9SF2 | chr13:g.99517631T>C |
hsa_circ_0030729 | TM9SF2 | chr13:g.99517645A>C |
hsa_circ_0030729 | TM9SF2 | chr13:g.99517648C>T |
hsa_circ_0030733 | TM9SF2 | chr13:g.99520058G>A |
hsa_circ_0030733 | TM9SF2 | chr13:g.99520068G>A |
hsa_circ_0030733 | TM9SF2 | chr13:g.99520090G>T |
hsa_circ_0030733 | TM9SF2 | chr13:g.99520099C>T |
hsa_circ_0030733 | TM9SF2 | chr13:g.99520107G>T |
hsa_circ_0030733 | TM9SF2 | chr13:g.99529487G>T |
hsa_circ_0030733 | TM9SF2 | chr13:g.99529531C>G |
hsa_circ_0030733 | TM9SF2 | chr13:g.99529533G>A |
hsa_circ_0030733 | TM9SF2 | chr13:g.99529559GA>G |
hsa_circ_0030733 | TM9SF2 | chr13:g.99536642G>A |
hsa_circ_0030733 | TM9SF2 | chr13:g.99537757G>C |
hsa_circ_0030733 | TM9SF2 | chr13:g.99537769A>G |
hsa_circ_0030733 | TM9SF2 | chr13:g.99537854A>G |
hsa_circ_0030733 | TM9SF2 | chr13:g.99537858G>A |
hsa_circ_0030733 | TM9SF2 | chr13:g.99539469A>C |
hsa_circ_0030733 | TM9SF2 | chr13:g.99539488C>T |
hsa_circ_0030733 | TM9SF2 | chr13:g.99539554C>T |
hsa_circ_0030733 | TM9SF2 | chr13:g.99539554C>A |
hsa_circ_0030733 | TM9SF2 | chr13:g.99539557G>T |
hsa_circ_0030736 | TM9SF2 | chr13:g.99540793G>A |
hsa_circ_0030736 | TM9SF2 | chr13:g.99541599A>G |
hsa_circ_0030736 | TM9SF2 | chr13:g.99541612T>G |
hsa_circ_0030736 | TM9SF2 | chr13:g.99541620C>G |
hsa_circ_0030736 | TM9SF2 | chr13:g.99541628G>A |
hsa_circ_0030736 | TM9SF2 | chr13:g.99541635G>T |
hsa_circ_0030737 | TM9SF2 | chr13:g.99543900A>G |
hsa_circ_0030737 | TM9SF2 | chr13:g.99543946C>T |
hsa_circ_0030737 | TM9SF2 | chr13:g.99543959G>T |
hsa_circ_0030738 | TM9SF2 | chr13:g.99547061G>T |
hsa_circ_0030739 | TM9SF2 | chr13:g.99552216G>C |
hsa_circ_0030739 | TM9SF2 | chr13:g.99552225G>A |
hsa_circ_0030739 | TM9SF2 | chr13:g.99552261G>T |
hsa_circ_0030739 | TM9SF2 | chr13:g.99552274G>A |
hsa_circ_0030739 | TM9SF2 | chr13:g.99552278A>G |
hsa_circ_0030739 | TM9SF2 | chr13:g.99552280C>T |
hsa_circ_0030739 | TM9SF2 | chr13:g.99552288C>G |
hsa_circ_0030739 | TM9SF2 | chr13:g.99554372G>T |
hsa_circ_0030739 | TM9SF2 | chr13:g.99554380C>T |
hsa_circ_0030738 | TM9SF2 | chr13:g.99555573C>T |
hsa_circ_0030738 | TM9SF2 | chr13:g.99555593T>G |
hsa_circ_0030738 | TM9SF2 | chr13:g.99555603T>A |
hsa_circ_0030738 | TM9SF2 | chr13:g.99555609G>T |
hsa_circ_0030738 | TM9SF2 | chr13:g.99555610C>T |
hsa_circ_0030738 | TM9SF2 | chr13:g.99555610C>A |
hsa_circ_0030738 | TM9SF2 | chr13:g.99555611A>G |
hsa_circ_0030738 | TM9SF2 | chr13:g.99559395G>A |
hsa_circ_0030738 | TM9SF2 | chr13:g.99559409C>T |
hsa_circ_0030738 | TM9SF2 | chr13:g.99559425C>G |
hsa_circ_0030738 | TM9SF2 | chr13:g.99559463C>T |
hsa_circ_0030738 | TM9SF2 | chr13:g.99559484T>G |
hsa_circ_0030738 | TM9SF2 | chr13:g.99559508T>G |
hsa_circ_0030736 | TM9SF2 | chr13:g.99562748A>G |
hsa_circ_0030736 | TM9SF2 | chr13:g.99562751T>C |
hsa_circ_0030736 | TM9SF2 | chr13:g.99562753G>T |