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_0044416
Gene Symbol: ZNF652
Browse Associations

Somatic mutations that impact miRNA target sites



Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317746A>G COSN9670055 C0021T [kidney][NS][other][neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-374a-3p actgttTGATAAatt CUUAUCAG m6b Created HPKTA_27763_G29822.1_47395075
hsa-miR-4477a actgtTTAATAaatt CUAUUAAG m6b Disrupted HPKTA_27763_G29822.1_47395075
hsa-miR-374a-3p actgttTGATAAatt CUUAUCAG m6b Created HPRT3_11558_G15291.1_47395110
hsa-miR-4477a actgtTTAATAaatt CUAUUAAG m6b Disrupted HPRT3_11558_G15291.1_47395110

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317715C>T COSM4382773 721LT [large_intestine][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-147a agCCACACAgccagt GUGUGUGG m7b (m7b->m6b) HPKTA_27763_G29822.1_47395075
hsa-miR-3064-5p agccacaCAGCCAGt UCUGGCUG m7b Disrupted HPKTA_27763_G29822.1_47395075
hsa-miR-4491 agCCACATagccagt AAUGUGGA m6b Created HPKTA_27763_G29822.1_47395075
hsa-miR-4657 agCCACATagccagt AAUGUGGA m6b Created HPKTA_27763_G29822.1_47395075
hsa-miR-4794 agccacaTAGCCAGt UCUGGCUA m7b Created HPKTA_27763_G29822.1_47395075
hsa-miR-644a aGCCACACagccagt AGUGUGGC m7b Disrupted HPKTA_27763_G29822.1_47395075
hsa-miR-6504-5p agccacaCAGCCAGt UCUGGCUG m7b Disrupted HPKTA_27763_G29822.1_47395075
hsa-miR-664a-5p agccacaTAGCCAGt ACUGGCUA m7b Created HPKTA_27763_G29822.1_47395075
hsa-miR-7108-5p aGCCACACagccagt GUGUGGCC m7a Disrupted HPKTA_27763_G29822.1_47395075
hsa-miR-7974 agccaCACAGCCagt AGGCUGUG m7b Disrupted HPKTA_27763_G29822.1_47395075

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317675G>A COSM1302979 TCGA-DK-A3IV-01 [urinary_tract][bladder][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-let-7a-2-3p gtgCTGTACAtgtag CUGUACAG m7b Created HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-let-7g-3p gtgCTGTACAtgtag CUGUACAG m7b Created HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-4666a-5p gtgctgtACATGTAg AUACAUGU m7b Created HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-let-7a-2-3p gtgCTGTACAtgtag CUGUACAG m7b Created HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-let-7g-3p gtgCTGTACAtgtag CUGUACAG m7b Created HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-4666a-5p gtgctgtACATGTAg AUACAUGU m7b Created HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317670T>C COSM189099 TCGA-AA-3984-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-187-5p gtgcaTGTAGCagga GGCUACAA m6b Disrupted HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-221-3p gtgcATGTAGCagga AGCUACAU m7b Disrupted HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-222-3p gtgcATGTAGCagga AGCUACAU m7b Disrupted HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-3692-5p gtgcatgCAGCAGGa CCUGCUGG m7a Created HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-370-3p gtgcatgCAGCAGGa GCCUGCUG m7b Created HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-548v gtgcaTGTAGCagga AGCUACAG m6b Disrupted HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-6893-3p gtgcatgCAGCAGGa CCCUGCUG m7b Created HHHNA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-187-5p gtgcaTGTAGCagga GGCUACAA m6b Disrupted HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-221-3p gtgcATGTAGCagga AGCUACAU m7b Disrupted HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-222-3p gtgcATGTAGCagga AGCUACAU m7b Disrupted HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-3692-5p gtgcatgCAGCAGGa CCUGCUGG m7a Created HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-370-3p gtgcatgCAGCAGGa GCCUGCUG m7b Created HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-548v gtgcaTGTAGCagga AGCUACAG m6b Disrupted HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
hsa-miR-6893-3p gtgcatgCAGCAGGa CCCUGCUG m7b Created HHHSA_10018_ZNF652|NM_001145365|exon_CDS|-6.34606562178752|3.03416202734739
Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317621C>T COSM4457793 CSCC-27-T [skin][head_neck][carcinoma][squamous_cell_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
chr17:g.49317517C>T COSM4746395 HSJD_DIPG008 [central_nervous_system][brainstem][glioma][astrocytoma_Grade_II]
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
chr17:g.49317506G>A COSM3819896 TCGA-AC-A23H-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6514-5p tCTCCATAaaacaga UAUGGAGU m7a Created HHKTA_16164_NM_001145365|649|688|4.41332998727923|0.205036145219504

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317463C>T COSM1679901 MDA-N [NS][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1324 gcagTGTCTGacgtg CCAGACAG m6b Disrupted HHFKP_60325_cluster-10430_35_162
hsa-miR-141-3p gCAGTGTTtgacgtg UAACACUG m7b Created HHFKP_60325_cluster-10430_35_162
hsa-miR-200a-3p gCAGTGTTtgacgtg UAACACUG m7b Created HHFKP_60325_cluster-10430_35_162

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317458G>A COSM1384070 TCGA-CM-6162-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4666b gtctgACATGCAtgc UUGCAUGU m7b Created HHFKP_60325_cluster-10430_35_162

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317440G>C COSM4982718 3N48-VS-3T48 [oesophagus][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4783-3p taaggaaCACCGGGa CCCCGGUG m7b Created HHHNE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-4783-3p taaggaaCACCGGGa CCCCGGUG m7b Created HHHSE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317432G>T COSM980779 TCGA-B5-A0JY-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-5571-5p accggGAGAATTctg CAAUUCUC m7b Disrupted HHHNE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-629-3p accGGGAGAAttctg GUUCUCCC m7b Disrupted HHHNE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-6867-3p accGGGAGAattctg CUCUCCCU m6b Disrupted HHHNE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-5571-5p accggGAGAATTctg CAAUUCUC m7b Disrupted HHHSE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-629-3p accGGGAGAAttctg GUUCUCCC m7b Disrupted HHHSE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-6867-3p accGGGAGAattctg CUCUCCCU m6b Disrupted HHHSE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317430A>G COSM126471 HN_62415 [upper_aerodigestive_tract][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4680-5p cgggAGAGTTCTgat AGAACUCU m8a Created HHHNE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-5571-5p cggGAGAATTctgat CAAUUCUC m7b Disrupted HHHNE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-629-3p cGGGAGAAttctgat GUUCUCCC m7b Disrupted HHHNE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-4680-5p cgggAGAGTTCTgat AGAACUCU m8a Created HHHSE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-5571-5p cggGAGAATTctgat CAAUUCUC m7b Disrupted HHHSE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329
hsa-miR-629-3p cGGGAGAAttctgat GUUCUCCC m7b Disrupted HHHSE_22294_ZNF652|NM_001145365|exon_CDS|-7.60897057046409|1.2373260250329

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317273T>C COSM3388001 8016470 [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1304-3p caagCAGTGAGgagg UCUCACUG m7b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-639 caaGCAGCGAggagg AUCGCUGC m7b Created HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6890-3p caaGCAGTGaggagg CCACUGCC m6b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-1304-3p caagCAGTGAGgagg UCUCACUG m7b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-639 caaGCAGCGAggagg AUCGCUGC m7b Created HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6890-3p caaGCAGTGaggagg CCACUGCC m6b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317266G>A COSM1384069 TCGA-AA-3968-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1236-3p tgaggaGGAAGAGGa CCUCUUCC m8a Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-1238-3p tgagGAGGAAGagga CUUCCUCG m7a Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-130b-5p tgaggaGAAAGAGga ACUCUUUC m7b Created HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-4279 tGAGGAGAaagagga CUCUCCUC m7b Created HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-4691-5p tgaGGAGGAagagga GUCCUCCA m6b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-5193 tGAGGAGGAagagga UCCUCCUC m8a (m8a->m7a) HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-629-3p tgaGGAGAAagagga GUUCUCCC m6b Created HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-660-3p tgAGGAGGaagagga ACCUCCUG m6b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6749-3p tgaGGAGGAagagga CUCCUCCC m6b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6792-3p tgaGGAGGAagagga CUCCUCCA m6b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-877-3p tgaggagGAAGAGGa UCCUCUUC m7b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-1236-3p tgaggaGGAAGAGGa CCUCUUCC m8a Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-1238-3p tgagGAGGAAGagga CUUCCUCG m7a Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-130b-5p tgaggaGAAAGAGga ACUCUUUC m7b Created HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-4279 tGAGGAGAaagagga CUCUCCUC m7b Created HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-4691-5p tgaGGAGGAagagga GUCCUCCA m6b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-5193 tGAGGAGGAagagga UCCUCCUC m8a (m8a->m7a) HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-629-3p tgaGGAGAAagagga GUUCUCCC m6b Created HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-660-3p tgAGGAGGaagagga ACCUCCUG m6b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6749-3p tgaGGAGGAagagga CUCCUCCC m6b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6792-3p tgaGGAGGAagagga CUCCUCCA m6b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-877-3p tgaggagGAAGAGGa UCCUCUUC m7b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49317242G>A COSM4067473 TCGA-CG-5723-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2682-3p ggAAGAGGCcacaga CGCCUCUU m7b (m7b->m6b) HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-4757-5p ggaAGAGGCCacaga AGGCCUCU m7b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-663b ggaagaGGCCACaga GGUGGCCC m6b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6744-3p ggaAGAGGCCacaga GGGCCUCU m7b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6781-3p ggAAGAGGCcacaga UGCCUCUU m7b (m7b->m6b) HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6843-3p ggaaGAGACCAcaga AUGGUCUC m7b Created HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6848-3p ggaaGAGACCACaga GUGGUCUC m8a Created HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6878-3p ggaaGAGGCCAcaga CUGGCCUC m7b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-7108-5p ggaagaGGCCACAga GUGUGGCC m7b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-877-3p gGAAGAGGccacaga UCCUCUUC m7b Disrupted HHHNE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-1236-3p GGAAGAGGccacaga CCUCUUCC m8a Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-2682-3p ggAAGAGGCcacaga CGCCUCUU m7b (m7b->m6b) HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-4757-5p ggaAGAGGCCacaga AGGCCUCU m7b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-663b ggaagaGGCCACaga GGUGGCCC m6b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6744-3p ggaAGAGGCCacaga GGGCCUCU m7b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6781-3p ggAAGAGGCcacaga UGCCUCUU m7b (m7b->m6b) HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6843-3p ggaaGAGACCAcaga AUGGUCUC m7b Created HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6848-3p ggaaGAGACCACaga GUGGUCUC m8a Created HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-6878-3p ggaaGAGGCCAcaga CUGGCCUC m7b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-7108-5p ggaagaGGCCACAga GUGUGGCC m7b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481
hsa-miR-877-3p gGAAGAGGccacaga UCCUCUUC m7b Disrupted HHHSE_22293_ZNF652|NM_001145365|exon_CDS|-7.56888550131005|-1.25084847632481

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49316879C>T COSM3518917 TCGA-D3-A51G-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3180-5p gtttgtcCTGGAAag CUUCCAGA m6b Disrupted HHHNE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-4436a gttTGTCCTGgaaag GCAGGACA m7b Disrupted HHHNE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-5000-3p gttTGTCCTGgaaag UCAGGACA m7b Disrupted HHHNE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-665 gtttgTCCTGGaaag ACCAGGAG m6b Disrupted HHHNE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-3180-5p gtttgtcCTGGAAag CUUCCAGA m6b Disrupted HHHNE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-4436a gttTGTCCTGgaaag GCAGGACA m7b Disrupted HHHNE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-5000-3p gttTGTCCTGgaaag UCAGGACA m7b Disrupted HHHNE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-665 gtttgTCCTGGaaag ACCAGGAG m6b Disrupted HHHNE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-3180-5p gtttgtcCTGGAAag CUUCCAGA m6b Disrupted HHHSE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-4436a gttTGTCCTGgaaag GCAGGACA m7b Disrupted HHHSE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-5000-3p gttTGTCCTGgaaag UCAGGACA m7b Disrupted HHHSE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-665 gtttgTCCTGGaaag ACCAGGAG m6b Disrupted HHHSE_22291_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-3180-5p gtttgtcCTGGAAag CUUCCAGA m6b Disrupted HHHSE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-4436a gttTGTCCTGgaaag GCAGGACA m7b Disrupted HHHSE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-5000-3p gttTGTCCTGgaaag UCAGGACA m7b Disrupted HHHSE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171
hsa-miR-665 gtttgTCCTGGaaag ACCAGGAG m6b Disrupted HHHSE_22292_ZNF652|NM_001145365|exon_CDS|-7.03307228611689|-1.39771916034171

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49312826C>T COSM3518915 TCGA-GN-A263-01 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-887-3p aacaaatCGTTCAag GUGAACGG m6b Disrupted HHFKP_60323_cluster-10430_33_18

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49312740A>T COSM1737032 P142 [large_intestine][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4659a-3p ttgtgAGAAGAAAtt UUUCUUCU m8a Disrupted HHFCT_63641_cluster-10430_36_2433
hsa-miR-4659b-3p ttgtgAGAAGAAAtt UUUCUUCU m8a Disrupted HHFCT_63641_cluster-10430_36_2433
hsa-miR-4798-3p ttGTGAGTagaaatt AACUCACG m6b Created HHFCT_63641_cluster-10430_36_2433
hsa-miR-6875-3p ttgtgaGAAGAAatt AUUCUUCC m6b Disrupted HHFCT_63641_cluster-10430_36_2433
hsa-miR-942-5p ttgtGAGAAGAaatt UCUUCUCU m7a Disrupted HHFCT_63641_cluster-10430_36_2433

Mutation Mutation ID Sample Name Cancer Type
chr17:g.49312727C>T COSM3889851 TCGA-FW-A3R5-06 [skin][NS][malignant_melanoma][NS]
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.

*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.

Genome Browser