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 [11 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
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NM_005066 | SFPQ | chr1:g.35187047G>A |
NM_005066 | SFPQ | chr1:g.35187048G>T |
NM_005066 | SFPQ | chr1:g.35187066G>C |
NM_005066 | SFPQ | chr1:g.35187079AGGT>T |
NM_005066 | SFPQ | chr1:g.35190751A>C |
NM_005066 | SFPQ | chr1:g.35190814C>T |
NM_005066 | SFPQ | chr1:g.35191471G>T |
NM_005066 | SFPQ | chr1:g.35191479C>AC |
NM_005066 | SFPQ | chr1:g.35191497G>T |
NM_005066 | SFPQ | chr1:g.35192683A>G |
NM_005066 | SFPQ | chr1:g.35192710G>A |
Somatic mutations that alter miRNA target sites: PAR-CLIP and HITS-CLIP [59 records found] |
[download data table] |
Transcript ID | Gene Symbol | Mutation ID |
---|---|---|
hsa_circ_0011531 | SFPQ | chr1:g.35184516A>G |
hsa_circ_0011531 | SFPQ | chr1:g.35184552T>G |
hsa_circ_0011531 | SFPQ | chr1:g.35184564G>T |
hsa_circ_0011531 | SFPQ | chr1:g.35184565C>T |
hsa_circ_0011531 | SFPQ | chr1:g.35187031C>T |
hsa_circ_0011531 | SFPQ | chr1:g.35187047G>A |
hsa_circ_0011531 | SFPQ | chr1:g.35187048G>T |
hsa_circ_0011531 | SFPQ | chr1:g.35187066G>C |
hsa_circ_0011531 | SFPQ | chr1:g.35187079AGGT>T |
hsa_circ_0011531 | SFPQ | chr1:g.35187089C>A |
hsa_circ_0011531 | SFPQ | chr1:g.35187206G>T |
hsa_circ_0011531 | SFPQ | chr1:g.35187224G>A |
hsa_circ_0011531 | SFPQ | chr1:g.35187225C>T |
hsa_circ_0011531 | SFPQ | chr1:g.35187235G>A |
hsa_circ_0011531 | SFPQ | chr1:g.35187236C>T |
hsa_circ_0011531 | SFPQ | chr1:g.35187992G>A |
hsa_circ_0011531 | SFPQ | chr1:g.35188008G>C |
hsa_circ_0011531 | SFPQ | chr1:g.35188016G>A |
hsa_circ_0011531 | SFPQ | chr1:g.35188047C>T |
hsa_circ_0011531 | SFPQ | chr1:g.35188067AAG>G |
hsa_circ_0011531 | SFPQ | chr1:g.35188077C>T |
hsa_circ_0011531 | SFPQ | chr1:g.35189046C>A |
hsa_circ_0011531 | SFPQ | chr1:g.35189236G>A |
hsa_circ_0011531 | SFPQ | chr1:g.35189247C>T |
hsa_circ_0011531 | SFPQ | chr1:g.35189258G>A |
hsa_circ_0011531 | SFPQ | chr1:g.35189270A>C |
hsa_circ_0011531 | SFPQ | chr1:g.35189320G>A |
hsa_circ_0011533 | SFPQ | chr1:g.35190502C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35190522C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35190523G>A |
hsa_circ_0011533 | SFPQ | chr1:g.35190751A>C |
hsa_circ_0011533 | SFPQ | chr1:g.35190814C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35190860G>T |
hsa_circ_0011533 | SFPQ | chr1:g.35190862A>G |
hsa_circ_0011533 | SFPQ | chr1:g.35190862A>C |
hsa_circ_0011533 | SFPQ | chr1:g.35190920C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35190933A>T |
hsa_circ_0011533 | SFPQ | chr1:g.35190952A>G |
hsa_circ_0011533 | SFPQ | chr1:g.35191351T>G |
hsa_circ_0011533 | SFPQ | chr1:g.35191360G>A |
hsa_circ_0011533 | SFPQ | chr1:g.35191394G>T |
hsa_circ_0011533 | SFPQ | chr1:g.35191415A>G |
hsa_circ_0011533 | SFPQ | chr1:g.35191434C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35191471G>T |
hsa_circ_0011533 | SFPQ | chr1:g.35191479C>AC |
hsa_circ_0011533 | SFPQ | chr1:g.35191497G>T |
hsa_circ_0011533 | SFPQ | chr1:g.35191510C>G |
hsa_circ_0011533 | SFPQ | chr1:g.35191515T>A |
hsa_circ_0011533 | SFPQ | chr1:g.35192302C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35192683A>G |
hsa_circ_0011533 | SFPQ | chr1:g.35192710G>A |
hsa_circ_0011533 | SFPQ | chr1:g.35192753G>A |
hsa_circ_0011533 | SFPQ | chr1:g.35192840A>G |
hsa_circ_0011533 | SFPQ | chr1:g.35192843G>T |
hsa_circ_0011533 | SFPQ | chr1:g.35192863C>A |
hsa_circ_0011533 | SFPQ | chr1:g.35192939C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35192950C>T |
hsa_circ_0011533 | SFPQ | chr1:g.35192966C>A |
hsa_circ_0011533 | SFPQ | chr1:g.35193012G>A |