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: hsa_circ_0088202
Gene Symbol: TNC
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Browse Pathways

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063116G>A COSM3903439 TCGA-HF-7132-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3126-3p ggaccacGCCAGATg CAUCUGGC m7b Disrupted HHHNA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-3650 ggacCACACCagatg AGGUGUGU m6b Created HHHNA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-4299 ggaccaCACCAGatg GCUGGUGA m6b Created HHHNA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-4456 ggaccaCACCAGatg CCUGGUGG m6b Created HHHNA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-548q ggaccaCACCAGatg GCUGGUGC m6b Created HHHNA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-7978 ggaccACACCAGAtg UCUGGUGU m8a Created HHHNA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-3126-3p ggaccacGCCAGATg CAUCUGGC m7b Disrupted HHHNE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-3650 ggacCACACCagatg AGGUGUGU m6b Created HHHNE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-4299 ggaccaCACCAGatg GCUGGUGA m6b Created HHHNE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-4456 ggaccaCACCAGatg CCUGGUGG m6b Created HHHNE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-548q ggaccaCACCAGatg GCUGGUGC m6b Created HHHNE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-7978 ggaccACACCAGAtg UCUGGUGU m8a Created HHHNE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-3126-3p ggaccacGCCAGATg CAUCUGGC m7b Disrupted HHHSA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-3650 ggacCACACCagatg AGGUGUGU m6b Created HHHSA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-4299 ggaccaCACCAGatg GCUGGUGA m6b Created HHHSA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-4456 ggaccaCACCAGatg CCUGGUGG m6b Created HHHSA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-548q ggaccaCACCAGatg GCUGGUGC m6b Created HHHSA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-7978 ggaccACACCAGAtg UCUGGUGU m8a Created HHHSA_22257_TNC|NM_002160|exon_CDS|-8.08481065689355|-1.31780496602962
hsa-miR-3126-3p ggaccacGCCAGATg CAUCUGGC m7b Disrupted HHHSE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-3650 ggacCACACCagatg AGGUGUGU m6b Created HHHSE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-4299 ggaccaCACCAGatg GCUGGUGA m6b Created HHHSE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-4456 ggaccaCACCAGatg CCUGGUGG m6b Created HHHSE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-548q ggaccaCACCAGatg GCUGGUGC m6b Created HHHSE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
hsa-miR-7978 ggaccACACCAGAtg UCUGGUGU m8a Created HHHSE_19262_TNC|NM_002160|exon_CDS|-7.63333113978549|0.29969777754092
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063042C>T COSM4168925 App2312 [peritoneum][appendix][other][pseudomyxoma_peritonei]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063032C>T COSM455231 TCGA-B6-A0IJ-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1911-3p ttCCTGGTagcctgc CACCAGGC m6b Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-5006-5p ttCCTGGCAgcctgc UUGCCAGG m7b (m7b->m6b) HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-665 tTCCTGGTagcctgc ACCAGGAG m7a Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6753-5p ttCCTGGTagcctgc CACCAGGG m6b Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-1911-3p ttCCTGGTagcctgc CACCAGGC m6b Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-5006-5p ttCCTGGCAgcctgc UUGCCAGG m7b (m7b->m6b) HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-665 tTCCTGGTagcctgc ACCAGGAG m7a Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6753-5p ttCCTGGTagcctgc CACCAGGG m6b Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063030G>C COSM1104449 TCGA-AP-A059-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063025C>T COSM486971 TCGA-BP-4973-01 [kidney][NS][carcinoma][clear_cell_renal_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4438 cAGCCTGTGttccat CACAGGCU m8a (m7a->m8a) HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6768-5p cagCCTGTGTtccat CACACAGG m7b Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-4438 cAGCCTGTGttccat CACAGGCU m8a (m7a->m8a) HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6768-5p cagCCTGTGTtccat CACACAGG m7b Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063021C>T COSM4427516 388 [upper_aerodigestive_tract][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-490-5p ctgcgtTCCATGGaa CCAUGGAU m7a Disrupted HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-8060 ctgcgtTTCATGGaa CCAUGAAG m7a Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-490-5p ctgcgtTCCATGGaa CCAUGGAU m7a Disrupted HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-8060 ctgcgtTTCATGGaa CCAUGAAG m7a Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063017G>A COSM228512 ME043T [skin][extremity][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-490-5p gtTCCATGGaaatcc CCAUGGAU m7a (m7a->m6a) HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-5581-3p gttcCATGGAAatcc UUCCAUGC m7a Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-7159-3p gttcCATAGAAAtcc UUUCUAUG m8a Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-490-5p gtTCCATGGaaatcc CCAUGGAU m7a (m7a->m6a) HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-5581-3p gttcCATGGAAatcc UUCCAUGC m7a Disrupted HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-7159-3p gttcCATAGAAAtcc UUUCUAUG m8a Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-490-5p gtTCCATGGaaatcc CCAUGGAU m7a (m7a->m6a) HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-5581-3p gttcCATGGAAatcc UUCCAUGC m7a Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-7159-3p gttcCATAGAAAtcc UUUCUAUG m8a Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-490-5p gtTCCATGGaaatcc CCAUGGAU m7a (m7a->m6a) HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-5581-3p gttcCATGGAAatcc UUCCAUGC m7a Disrupted HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-7159-3p gttcCATAGAAAtcc UUUCUAUG m8a Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115063012T>C COSM1229856 587284 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-193b-5p atggAAACCCCaggc CGGGGUUU m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3167 atgGAAATCCcaggc AGGAUUUC m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3170 atggaAACCCCAGgc CUGGGGUU m8a Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-5089-5p atggaAATCCCAggc GUGGGAUU m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-619-5p atggaaATCCCAGgc GCUGGGAU m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6506-5p atggaaATCCCAGgc ACUGGGAU m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6852-5p atggaaaCCCCAGGc CCCUGGGG m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6855-5p atggaAACCCCAggc UUGGGGUU m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-7155-5p atggaaACCCCAGgc UCUGGGGU m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-876-5p atgGAAATCCcaggc UGGAUUUC m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-193b-5p atggAAACCCCaggc CGGGGUUU m7b Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-3167 atgGAAATCCcaggc AGGAUUUC m7b Disrupted HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-3170 atggaAACCCCAGgc CUGGGGUU m8a Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-5089-5p atggaAATCCCAggc GUGGGAUU m7b Disrupted HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-619-5p atggaaATCCCAGgc GCUGGGAU m7b Disrupted HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6506-5p atggaaATCCCAGgc ACUGGGAU m7b Disrupted HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6852-5p atggaaaCCCCAGGc CCCUGGGG m7b Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6855-5p atggaAACCCCAggc UUGGGGUU m7b Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-7155-5p atggaaACCCCAGgc UCUGGGGU m7b Created HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-876-5p atgGAAATCCcaggc UGGAUUUC m7b Disrupted HHHNE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-193b-5p atggAAACCCCaggc CGGGGUUU m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3167 atgGAAATCCcaggc AGGAUUUC m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3170 atggaAACCCCAGgc CUGGGGUU m8a Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-5089-5p atggaAATCCCAggc GUGGGAUU m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-619-5p atggaaATCCCAGgc GCUGGGAU m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6506-5p atggaaATCCCAGgc ACUGGGAU m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6852-5p atggaaaCCCCAGGc CCCUGGGG m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6855-5p atggaAACCCCAggc UUGGGGUU m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-7155-5p atggaaACCCCAGgc UCUGGGGU m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-876-5p atgGAAATCCcaggc UGGAUUUC m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-193b-5p atggAAACCCCaggc CGGGGUUU m7b Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-3167 atgGAAATCCcaggc AGGAUUUC m7b Disrupted HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-3170 atggaAACCCCAGgc CUGGGGUU m8a Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-5089-5p atggaAATCCCAggc GUGGGAUU m7b Disrupted HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-619-5p atggaaATCCCAGgc GCUGGGAU m7b Disrupted HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6506-5p atggaaATCCCAGgc ACUGGGAU m7b Disrupted HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6852-5p atggaaaCCCCAGGc CCCUGGGG m7b Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-6855-5p atggaAACCCCAggc UUGGGGUU m7b Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-7155-5p atggaaACCCCAGgc UCUGGGGU m7b Created HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284
hsa-miR-876-5p atgGAAATCCcaggc UGGAUUUC m7b Disrupted HHHSE_19261_TNC|NM_002160|exon_CDS|-8.17452440667316|-0.770467325656284

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115062992A>C COSM1459566 TCGA-AZ-5407-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1202 gGCTGGCACtcctta GUGCCAGC m8a (m8a->m7a) HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-1909-5p ggctGGCACTCctta UGAGUGCC m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3173-3p ggctggcCCTCCTTa AAAGGAGG m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3194-5p GGCTGGCCctcctta GGCCAGCC m8a Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3972 gGCTGGCActcctta CUGCCAGC m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4433b-3p ggctggCACTCCTta CAGGAGUG m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4640-5p ggCTGGCCCtcctta UGGGCCAG m7b (m6b->m7b) HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4726-5p ggCTGGCCCTcctta AGGGCCAG m8a Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4779 ggctggCCCTCCTta UAGGAGGG m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-504-3p ggctgGCACTCCtta GGGAGUGC m7b Disrupted HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6891-5p ggctggcCCTCCTTa UAAGGAGG m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6895-5p ggcTGGCCCTcctta CAGGGCCA m7b Created HHHNA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-1202 gGCTGGCACtcctta GUGCCAGC m8a (m8a->m7a) HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-1909-5p ggctGGCACTCctta UGAGUGCC m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3173-3p ggctggcCCTCCTTa AAAGGAGG m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3194-5p GGCTGGCCctcctta GGCCAGCC m8a Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-3972 gGCTGGCActcctta CUGCCAGC m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4433b-3p ggctggCACTCCTta CAGGAGUG m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4640-5p ggCTGGCCCtcctta UGGGCCAG m7b (m6b->m7b) HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4726-5p ggCTGGCCCTcctta AGGGCCAG m8a Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-4779 ggctggCCCTCCTta UAGGAGGG m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-504-3p ggctgGCACTCCtta GGGAGUGC m7b Disrupted HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6891-5p ggctggcCCTCCTTa UAAGGAGG m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757
hsa-miR-6895-5p ggcTGGCCCTcctta CAGGGCCA m7b Created HHHSA_22256_TNC|NM_002160|exon_CDS|-8.43175148088449|-1.91089143445757

*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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