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_001178117
Gene Symbol: MINPP1
Browse Pathways

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr10:g.87508397G>A COSM2154887 TCGA-14-0865 [central_nervous_system][brain][glioma][astrocytoma_Grade_IV]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1229-3p actGTGAGAagtttt CUCUCACC m6b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-27a-3p ACTGTGAAaagtttt UUCACAGU m8a Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-27b-3p ACTGTGAAaagtttt UUCACAGU m8a Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-342-3p acTGTGAGAagtttt UCUCACAC m7a (m7a->m6a) HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-5003-3p actgtGAAAAGTttt UACUUUUC m7b Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-5096 actGTGAAAagtttt GUUUCACC m6b Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-513a-5p aCTGTGAAaagtttt UUCACAGG m7a Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329

Mutation Mutation ID Sample Name Cancer Type
chr10:g.87508396A>C COSM2154886 TCGA-14-0865 [central_nervous_system][brain][glioma][astrocytoma_Grade_IV]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1229-3p cactGTGAGAagttt CUCUCACC m6b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-128-3p CACTGTGAgaagttt UCACAGUG m8a Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-216a-3p CACTGTGAgaagttt UCACAGUG m8a Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-27a-3p cACTGTGAgaagttt UUCACAGU m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-27b-3p cACTGTGAgaagttt UUCACAGU m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-342-3p cacTGTGAGAagttt UCUCACAC m7a Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329

Mutation Mutation ID Sample Name Cancer Type
chr10:g.87508395G>C COSM415424 TCGA-C4-A0F1-01 [urinary_tract][bladder][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1229-3p tcactGTGAGAagtt CUCUCACC m6b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-128-3p tCACTGTGAgaagtt UCACAGUG m8a (m8a->m7a) HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-216a-3p tCACTGTGAgaagtt UCACAGUG m8a (m8a->m7a) HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-27a-3p tcACTGTGAgaagtt UUCACAGU m7b (m7b->m6b) HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-27b-3p tcACTGTGAgaagtt UUCACAGU m7b (m7b->m6b) HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-342-3p tcacTGTGAGAagtt UCUCACAC m7a Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-3660 tcaCTGTCAGaagtt ACUGACAG m7b Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-3681-3p tCACTGTGagaagtt ACACAGUG m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-4256 tcactGTCAGAagtt AUCUGACC m6b Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-4526 tcaCTGTCAGaagtt GCUGACAG m7b Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-6719-3p tcacTGTCAGAagtt UCUGACAU m7a Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-6730-3p tcacTGTCAGaagtt CCUGACAC m6b Created HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329

Mutation Mutation ID Sample Name Cancer Type
chr10:g.87508389C>T COSM4505391 CSCC-27-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1245a ttttGATCACTgtga AAGUGAUC m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-128-3p ttttgatCACTGTGa UCACAGUG m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-216a-3p ttttgatCACTGTGa UCACAGUG m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-3681-3p ttttgatCACTGTGa ACACAGUG m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-8079 ttttGATCACTGtga CAGUGAUC m8a Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-1245a ttttGATCACTgtga AAGUGAUC m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-128-3p ttttgatCACTGTGa UCACAGUG m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-216a-3p ttttgatCACTGTGa UCACAGUG m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-3681-3p ttttgatCACTGTGa ACACAGUG m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-8079 ttttGATCACTGtga CAGUGAUC m8a Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329

Mutation Mutation ID Sample Name Cancer Type
chr10:g.87508386G>T COSM1349443 TCGA-CM-6163-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1245a attttttGATCACTg AAGUGAUC m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-3613-3p aTTTTTTGatcactg ACAAAAAA m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329
hsa-miR-8079 attttttGATCACTg CAGUGAUC m7b Disrupted HHHSH_2298_MINPP1|NM_001178117|exon_CDS|-5.67609343833957|1.27363369285329

*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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