SomamiR DB 2.0
Somatic mutations altering microRNA-ceRNA interactions
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PolymiRTS Database
Prediction criteria: TargetScan sites only     All 6mer or longer seed matches
Transcript ID: NM_001017392
Gene Symbol: SUGP2

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr19:g.18995218G>A COSM3989820 TCGA-P4-A5E7-01 [kidney][NS][carcinoma][papillary_renal_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4310 tccagATGCTGCaga GCAGCAUU m7a Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-17-3p tccagatACTGCAGa ACUGCAGU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-7156-3p tccagatGCTGCAGa CUGCAGCC m7a Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4310 tccagATGCTGCaga GCAGCAUU m7a Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-7156-3p tccagatGCTGCAGa CUGCAGCC m7a Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-103a-3p tccagATGCTGCaga AGCAGCAU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-107 tccagATGCTGCaga AGCAGCAU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-1184 tccagatGCTGCAGa CCUGCAGC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-103a-3p tccagATGCTGCaga AGCAGCAU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-107 tccagATGCTGCaga AGCAGCAU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-1184 tccagatGCTGCAGa CCUGCAGC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-17-3p tccagatACTGCAGa ACUGCAGU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4310 tccagATGCTGCaga GCAGCAUU m7a Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-7156-3p tccagatGCTGCAGa CUGCAGCC m7a Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-103a-3p tccagATGCTGCaga AGCAGCAU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-107 tccagATGCTGCaga AGCAGCAU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-1184 tccagatGCTGCAGa CCUGCAGC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-17-3p tccagatACTGCAGa ACUGCAGU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849

Mutation Mutation ID Sample Name Cancer Type
chr19:g.18995193G>A COSM4541833 CSCC-7-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-328-3p gaaggAGGGCCAtgg CUGGCCCU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4290 gaaGGAGGGCcatgg UGCCCUCC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4667-3p gaAGGAGGGccatgg UCCCUCCU m7b (m7b->m6b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6775-3p gaaggAGGGCCatgg AGGCCCUG m6b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6822-3p gaaggAGAGCCatgg AGGCUCUA m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6845-3p gaAGGAGAGccatgg CCUCUCCU m7b (m6b->m7b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-760 gaaggAGAGCCatgg CGGCUCUG m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-8057 gaaggAGAGCCAtgg GUGGCUCU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-328-3p gaaggAGGGCCAtgg CUGGCCCU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4290 gaaGGAGGGCcatgg UGCCCUCC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4667-3p gaAGGAGGGccatgg UCCCUCCU m7b (m7b->m6b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6775-3p gaaggAGGGCCatgg AGGCCCUG m6b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6822-3p gaaggAGAGCCatgg AGGCUCUA m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6845-3p gaAGGAGAGccatgg CCUCUCCU m7b (m6b->m7b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-760 gaaggAGAGCCatgg CGGCUCUG m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-8057 gaaggAGAGCCAtgg GUGGCUCU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-328-3p gaaggAGGGCCAtgg CUGGCCCU m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4290 gaaGGAGGGCcatgg UGCCCUCC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4667-3p gaAGGAGGGccatgg UCCCUCCU m7b (m7b->m6b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6775-3p gaaggAGGGCCatgg AGGCCCUG m6b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6822-3p gaaggAGAGCCatgg AGGCUCUA m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6845-3p gaAGGAGAGccatgg CCUCUCCU m7b (m6b->m7b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-760 gaaggAGAGCCatgg CGGCUCUG m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-8057 gaaggAGAGCCAtgg GUGGCUCU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849

Mutation Mutation ID Sample Name Cancer Type
chr19:g.18995190C>T COSM342888 LUAD-S00484 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-103b ggagGGCTATGgcct UCAUAGCC m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-129-1-3p ggAGGGCTatggcct AAGCCCUU m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-129-2-3p ggAGGGCTatggcct AAGCCCUU m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-328-3p ggAGGGCCAtggcct CUGGCCCU m7b (m7b->m6b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-3651 ggaGGGCTATGgcct CAUAGCCC m8a Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4687-5p gGAGGGCTatggcct CAGCCCUC m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6775-3p ggAGGGCCatggcct AGGCCCUG m6b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849

Mutation Mutation ID Sample Name Cancer Type
chr19:g.18995176C>T COSM3891985 TCGA-FW-A3R5-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4419a tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6827-5p tgGGCTCCCtcggaa UGGGAGCC m7b (m7b->m6b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4419a tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6827-5p tgGGCTCCCtcggaa UGGGAGCC m7b (m7b->m6b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4419a tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 tgggCTCCCTCggaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6827-5p tgGGCTCCCtcggaa UGGGAGCC m7b (m7b->m6b) HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849

Mutation Mutation ID Sample Name Cancer Type
chr19:g.18995175CCC>TTC COSM4566111 CSCC-31-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4419a ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6827-5p ctgGGCTCCCtcggaaa UGGGAGCC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4419a ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6827-5p ctgGGCTCCCtcggaaa UGGGAGCC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4419a ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 ctgggCTCCCTCggaaa UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6827-5p ctgGGCTCCCtcggaaa UGGGAGCC m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849

Mutation Mutation ID Sample Name Cancer Type
chr19:g.18995173C>A COSM4947940 TCGA-CA-6717-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3124-3p gctccctAGGAAAGg ACUUUCCU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-384 gctccCTAGGAAagg AUUCCUAG m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4419a gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-5571-3p gctcCCTAGGAaagg GUCCUAGG m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-7975 gctccCTAGGAaagg AUCCUAGU m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-3124-3p gctccctAGGAAAGg ACUUUCCU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-384 gctccCTAGGAAagg AUUCCUAG m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4419a gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-5571-3p gctcCCTAGGAaagg GUCCUAGG m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-7975 gctccCTAGGAaagg AUCCUAGU m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-3124-3p gctccctAGGAAAGg ACUUUCCU m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-384 gctccCTAGGAAagg AUUCCUAG m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4419a gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-4510 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-5571-3p gctcCCTAGGAaagg GUCCUAGG m7b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6127 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6129 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6130 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-6133 gCTCCCTCggaaagg UGAGGGAG m7b Disrupted HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849
hsa-miR-7975 gctccCTAGGAaagg AUCCUAGU m6b Created HHHNA_12156_SUGP2|NM_001017392|exon_CDS|-6.91145778915597|-1.03316177032849

*By default, only target sites identified by TargetScan are displayed. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.

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