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_001017528
Gene Symbol: PRR5

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732355GC>G COSM4718117 T3503 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4688 cccgtgTGCCCCTgc UAGGGGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6743-5p cccgtgTGCCCCTgc AAGGGGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6805-5p cccgtgtGCCCCCTgc UAGGGGGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4688 cccgtgTGCCCCTgc UAGGGGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6743-5p cccgtgTGCCCCTgc AAGGGGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6805-5p cccgtgtGCCCCCTgc UAGGGGGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4688 cccgtgTGCCCCTgc UAGGGGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6743-5p cccgtgTGCCCCTgc AAGGGGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6805-5p cccgtgtGCCCCCTgc UAGGGGGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732352T>C COSM4156377 PTC-10C [thyroid][NS][other][neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3186-3p atgcCCGCGTGcccc UCACGCGG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 atgCCCGTGTgcccc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3186-3p atgcCCGCGTGcccc UCACGCGG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 atgCCCGTGTgcccc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3186-3p atgcCCGCGTGcccc UCACGCGG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 atgCCCGTGTgcccc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732350C>T COSM1416744 HCC27T [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-602 ccatgCCCGTGTgcc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6768-5p ccatgCCTGTGTGcc CACACAGG m8a Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p cCATGCCCGtgtgcc CGGGCAUG m8a (m8a->m7a) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3622b-5p CCATGCCTgtgtgcc AGGCAUGG m8a Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 cCATGCCCgtgtgcc AGGGCAUG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 ccatgCCCGTGTgcc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6768-5p ccatgCCTGTGTGcc CACACAGG m8a Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p cCATGCCCGtgtgcc CGGGCAUG m8a (m8a->m7a) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3622b-5p CCATGCCTgtgtgcc AGGCAUGG m8a Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 cCATGCCCgtgtgcc AGGGCAUG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 ccatgCCCGTGTgcc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6768-5p ccatgCCTGTGTGcc CACACAGG m8a Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p cCATGCCCGtgtgcc CGGGCAUG m8a (m8a->m7a) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3622b-5p CCATGCCTgtgtgcc AGGCAUGG m8a Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 cCATGCCCgtgtgcc AGGGCAUG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732349C>T COSM1722554 2_PRE-TREATMENT [NS][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4253 ccCATGCCCgtgtgc AGGGCAUG m7b (m7b->m6b) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 cccatgCCCGTGTgc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p ccCATGCCCGtgtgc CGGGCAUG m8a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 ccCATGCCCgtgtgc AGGGCAUG m7b (m7b->m6b) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 cccatgCCCGTGTgc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p ccCATGCCCGtgtgc CGGGCAUG m8a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 ccCATGCCCgtgtgc AGGGCAUG m7b (m7b->m6b) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 cccatgCCCGTGTgc GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p ccCATGCCCGtgtgc CGGGCAUG m8a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732348C>T COSM1714466 YUKLAB [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3622b-5p gcCCATGCCcgtgtg AGGCAUGG m7b (m7b->m6b) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 gccCATGCCCgtgtg AGGGCAUG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 gcccatgCCCGTGTg GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p gccCATGCCCGtgtg CGGGCAUG m8a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3622b-5p gcCCATGCCcgtgtg AGGCAUGG m7b (m7b->m6b) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 gccCATGCCCgtgtg AGGGCAUG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 gcccatgCCCGTGTg GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p gccCATGCCCGtgtg CGGGCAUG m8a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3622b-5p gcCCATGCCcgtgtg AGGCAUGG m7b (m7b->m6b) HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4253 gccCATGCCCgtgtg AGGGCAUG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-602 gcccatgCCCGTGTg GACACGGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6862-5p gccCATGCCCGtgtg CGGGCAUG m8a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732340G>C COSM4718113 T3301 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1538 tggcCCGGGCCcatg CGGCCCGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-2277-5p tggCCCGCGCccatg AGCGCGGG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-296-5p tggcccGGGCCCatg AGGGCCCC m6b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3178 tggccCGCGCCCatg GGGGCGCG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4745-3p tggcCCGGGCCcatg UGGCCCGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6724-5p tggcccGGGCCCAtg CUGGGCCC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6773-5p tggcccGGGCCCAtg UUGGGCCC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-1538 tggcCCGGGCCcatg CGGCCCGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-2277-5p tggCCCGCGCccatg AGCGCGGG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-296-5p tggcccGGGCCCatg AGGGCCCC m6b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3178 tggccCGCGCCCatg GGGGCGCG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4745-3p tggcCCGGGCCcatg UGGCCCGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6724-5p tggcccGGGCCCAtg CUGGGCCC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6773-5p tggcccGGGCCCAtg UUGGGCCC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-1538 tggcCCGGGCCcatg CGGCCCGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-2277-5p tggCCCGCGCccatg AGCGCGGG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-296-5p tggcccGGGCCCatg AGGGCCCC m6b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3178 tggccCGCGCCCatg GGGGCGCG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4745-3p tggcCCGGGCCcatg UGGCCCGG m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6724-5p tggcccGGGCCCAtg CUGGGCCC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-6773-5p tggcccGGGCCCAtg UUGGGCCC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732331G>A COSM1034967 TCGA-D1-A16J-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-148a-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-148b-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-152-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-1825 aggatGCACTGGccc UCCAGUGC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4738-5p aggatGCGCTGGccc ACCAGCGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-148a-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-148b-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-152-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-1825 aggatGCACTGGccc UCCAGUGC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4738-5p aggatGCGCTGGccc ACCAGCGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-148a-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-148b-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-152-3p aggaTGCACTGgccc UCAGUGCA m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-1825 aggatGCACTGGccc UCCAGUGC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4738-5p aggatGCGCTGGccc ACCAGCGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732323G>C COSM4835822 TCGA-Q1-A73O-01 [cervix][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1251-5p gaaGCTAGAGgatgc ACUCUAGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3137 gaaGCTACAGgatgc UCUGUAGC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4793-5p gaagctaCAGGATGc ACAUCCUG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-517-5p gaagCTAGAGGatgc CCUCUAGA m7a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-5196-3p gaagctaGAGGATGc UCAUCCUC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-1251-5p gaaGCTAGAGgatgc ACUCUAGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3137 gaaGCTACAGgatgc UCUGUAGC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4793-5p gaagctaCAGGATGc ACAUCCUG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-517-5p gaagCTAGAGGatgc CCUCUAGA m7a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-5196-3p gaagctaGAGGATGc UCAUCCUC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-1251-5p gaaGCTAGAGgatgc ACUCUAGC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3137 gaaGCTACAGgatgc UCUGUAGC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4793-5p gaagctaCAGGATGc ACAUCCUG m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-517-5p gaagCTAGAGGatgc CCUCUAGA m7a Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-5196-3p gaagctaGAGGATGc UCAUCCUC m7b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

Mutation Mutation ID Sample Name Cancer Type
chr22:g.44732316G>C COSM1130410 TCGA-EJ-5517-01 [prostate][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-216b-3p tcAGTGTGaagctag ACACACUU m6b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3117-5p tcAGTGTCaagctag AGACACUA m6b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-377-3p tcaGTGTGAagctag AUCACACA m6b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4453 tcagtgtCAAGCTag GAGCUUGG m6b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4538 tcagtgtCAAGCTag GAGCUUGG m6b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-514a-3p tcaGTGTCAAgctag AUUGACAC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-514b-3p tcaGTGTCAAgctag AUUGACAC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-216b-3p tcAGTGTGaagctag ACACACUU m6b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-3117-5p tcAGTGTCaagctag AGACACUA m6b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-377-3p tcaGTGTGAagctag AUCACACA m6b Disrupted HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4453 tcagtgtCAAGCTag GAGCUUGG m6b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-4538 tcagtgtCAAGCTag GAGCUUGG m6b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-514a-3p tcaGTGTCAAgctag AUUGACAC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358
hsa-miR-514b-3p tcaGTGTCAAgctag AUUGACAC m7b Created HHHNA_15863_PRR5|NM_001017529|exon_CDS|-1.43434418508885|-2.13373563273358

*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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