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_0018999
Gene Symbol: GRID1
Browse Associations
Browse Pathways

Somatic mutations that impact miRNA target sites



Mutation Mutation ID Sample Name Cancer Type
chr10:g.86264753T>A COSN7073506 8033414 [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA3_3065_G4656.1_88024515
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPTA3_3065_G4656.1_88024515
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPTA4_525_G2484.1_88024504
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPTA4_525_G2484.1_88024504
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA4_525_G2484.1_88024504
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA4_525_G2484.1_88024504
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA4_525_G2484.1_88024504
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA4_525_G2484.1_88024504
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA4_525_G2484.1_88024504
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA4_525_G2484.1_88024504
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPTA4_525_G2484.1_88024504
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPTK1_5115_G6012.1_88024515
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPTK1_5115_G6012.1_88024515
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTK1_5115_G6012.1_88024515
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTK1_5115_G6012.1_88024515
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTK1_5115_G6012.1_88024515
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTK1_5115_G6012.1_88024515
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTK1_5115_G6012.1_88024515
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTK1_5115_G6012.1_88024515
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPTK1_5115_G6012.1_88024515
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPKMA_2314_G2681.1_88024510
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPKMA_2314_G2681.1_88024510
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPKMA_2314_G2681.1_88024510
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPKMA_2314_G2681.1_88024510
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPKMA_2314_G2681.1_88024510
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPKMA_2314_G2681.1_88024510
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPKMA_2314_G2681.1_88024510
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPKMA_2314_G2681.1_88024510
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPKMA_2314_G2681.1_88024510
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPKMB_1224_G1364.1_88024515
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPKMB_1224_G1364.1_88024515
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPKMB_1224_G1364.1_88024515
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPKMB_1224_G1364.1_88024515
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPKMB_1224_G1364.1_88024515
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPKMB_1224_G1364.1_88024515
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPKMB_1224_G1364.1_88024515
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPKMB_1224_G1364.1_88024515
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPKMB_1224_G1364.1_88024515
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPKTA_9751_G10405.1_88024515
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPKTA_9751_G10405.1_88024515
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPKTA_9751_G10405.1_88024515
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPKTA_9751_G10405.1_88024515
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPKTA_9751_G10405.1_88024515
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPKTA_9751_G10405.1_88024515
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPKTA_9751_G10405.1_88024515
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPKTA_9751_G10405.1_88024515
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPKTA_9751_G10405.1_88024515
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPRO6_12824_G14882.1_88024515
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPRO6_12824_G14882.1_88024515
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPRO6_12824_G14882.1_88024515
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPRO6_12824_G14882.1_88024515
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPRO6_12824_G14882.1_88024515
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPRO6_12824_G14882.1_88024515
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPRO6_12824_G14882.1_88024515
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPRO6_12824_G14882.1_88024515
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPRO6_12824_G14882.1_88024515
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPRO8_2465_G3181.1_88024514
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPRO8_2465_G3181.1_88024514
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPRO8_2465_G3181.1_88024514
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPRO8_2465_G3181.1_88024514
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPRO8_2465_G3181.1_88024514
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPRO8_2465_G3181.1_88024514
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPRO8_2465_G3181.1_88024514
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPRO8_2465_G3181.1_88024514
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPRO8_2465_G3181.1_88024514
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPTA1_1904_G2630.1_88024505
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPTA1_1904_G2630.1_88024505
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA1_1904_G2630.1_88024505
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA1_1904_G2630.1_88024505
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA1_1904_G2630.1_88024505
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA1_1904_G2630.1_88024505
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA1_1904_G2630.1_88024505
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA1_1904_G2630.1_88024505
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPTA1_1904_G2630.1_88024505
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPTA2_253_G781.1_88024504
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPTA2_253_G781.1_88024504
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA2_253_G781.1_88024504
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA2_253_G781.1_88024504
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA2_253_G781.1_88024504
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA2_253_G781.1_88024504
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA2_253_G781.1_88024504
hsa-miR-6893-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA2_253_G781.1_88024504
hsa-miR-940 gcatgCCTGCCTctc AAGGCAGG m7b Disrupted HPTA2_253_G781.1_88024504
hsa-miR-1827 gcatgcCTGCCTCtc UGAGGCAG m7b Disrupted HPTA3_3065_G4656.1_88024515
hsa-miR-4720-5p gcATGCCAGcctctc CCUGGCAU m7b (m6b->m7b) HPTA3_3065_G4656.1_88024515
hsa-miR-4799-3p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA3_3065_G4656.1_88024515
hsa-miR-485-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA3_3065_G4656.1_88024515
hsa-miR-5588-5p gcATGCCAGcctctc ACUGGCAU m7b (m6b->m7b) HPTA3_3065_G4656.1_88024515
hsa-miR-6808-5p gcatgCCTGCCTctc CAGGCAGG m7b Disrupted HPTA3_3065_G4656.1_88024515
hsa-miR-6884-5p gcatgcCAGCCTCTc AGAGGCUG m8a Created HPTA3_3065_G4656.1_88024515

Mutation Mutation ID Sample Name Cancer Type
chr10:g.86264711G>A COSN2492223
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2682-5p gcctgcaACTGCCTg CAGGCAGU m7b Created HPRO6_12823_G14881.1_88024487
hsa-miR-34b-5p gcctgcaACTGCCTg UAGGCAGU m7b Created HPRO6_12823_G14881.1_88024487
hsa-miR-449c-5p gcctgcaACTGCCTg UAGGCAGU m7b Created HPRO6_12823_G14881.1_88024487
hsa-miR-548au-3p gcctgcAACTGCCtg UGGCAGUU m7b Created HPRO6_12823_G14881.1_88024487
hsa-miR-6511b-5p GCCTGCAGctgcctg CUGCAGGC m8a Disrupted HPRO6_12823_G14881.1_88024487
Mutation Mutation ID Sample Name Cancer Type
chr10:g.86030332A>G COSN7073412 8066452 [pancreas][NS][carcinoma][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.


Mutation Mutation ID Sample Name Cancer Type
chr10:g.85869131G>A COSM3441159 TCGA-EE-A2MS-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3124-3p cttGGAAAGatgacc ACUUUCCU m6b Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3667-3p cttGGAAGGatgacc ACCUUCCU m6b Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4793-5p cttggaAGGATGacc ACAUCCUG m6b Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-6734-3p cttGGAAGGatgacc CCCUUCCC m6b Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3124-3p cttGGAAAGatgacc ACUUUCCU m6b Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3667-3p cttGGAAGGatgacc ACCUUCCU m6b Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4793-5p cttggaAGGATGacc ACAUCCUG m6b Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-6734-3p cttGGAAGGatgacc CCCUUCCC m6b Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099

Mutation Mutation ID Sample Name Cancer Type
chr10:g.85869130G>A COSM4560141 CSCC-27-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3667-3p ttGGAAGGatgaccg ACCUUCCU m6b Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4793-5p ttggaAGGATGaccg ACAUCCUG m6b Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-6734-3p ttGGAAGGatgaccg CCCUUCCC m6b Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-6875-3p ttGGAAGAATgaccg AUUCUUCC m8a Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3667-3p ttGGAAGGatgaccg ACCUUCCU m6b Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4793-5p ttggaAGGATGaccg ACAUCCUG m6b Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-6734-3p ttGGAAGGatgaccg CCCUUCCC m6b Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-6875-3p ttGGAAGAATgaccg AUUCUUCC m8a Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099

Mutation Mutation ID Sample Name Cancer Type
chr10:g.85869117C>T COSM685153 TCGA-60-2707-01 [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1202 cgtggtCTGGCAaat GUGCCAGC m6b Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3972 cgtggtCTGGCAaat CUGCCAGC m6b Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4442 cgtgGTCCGGCaaat GCCGGACA m7a Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4776-3p cgtggtcTGGCAAat CUUGCCAU m6b Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-5006-5p cgtggtCTGGCAAat UUGCCAGG m7a Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-1202 cgtggtCTGGCAaat GUGCCAGC m6b Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3972 cgtggtCTGGCAaat CUGCCAGC m6b Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4442 cgtgGTCCGGCaaat GCCGGACA m7a Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4776-3p cgtggtcTGGCAAat CUUGCCAU m6b Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-5006-5p cgtggtCTGGCAAat UUGCCAGG m7a Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099

Mutation Mutation ID Sample Name Cancer Type
chr10:g.85869116G>A COSM271284 TCGA-AA-3833-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1287-5p gtggTCCAGCAaatc UGCUGGAU m7a Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3135b gtggTCCAGCaaatc GGCUGGAG m6b Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4442 gtgGTCCGGCaaatc GCCGGACA m7a Disrupted HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4776-5p gTGGTCCAgcaaatc GUGGACCA m7b Created HHHNE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-1287-5p gtggTCCAGCAaatc UGCUGGAU m7a Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-3135b gtggTCCAGCaaatc GGCUGGAG m6b Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4442 gtgGTCCGGCaaatc GCCGGACA m7a Disrupted HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099
hsa-miR-4776-5p gTGGTCCAgcaaatc GUGGACCA m7b Created HHHSE_7416_GRID1|NM_017551|exon_CDS|-4.15827289293481|-0.970433997803099

*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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