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_0077510
Gene Symbol: HACE1
Browse Associations

Somatic mutations that impact miRNA target sites



Mutation Mutation ID Sample Name Cancer Type
chr6:g.104785186C>T COSM3619132 TCGA-FS-A1ZS-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-103a-3p gATGCTGCTtccatt AGCAGCAU m8a (m8a->m7a) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-107 gATGCTGCTtccatt AGCAGCAU m8a (m8a->m7a) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-15a-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-15b-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-16-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-195-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-3688-3p gatgctgTTTCCATt UAUGGAAA m7b Created HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-424-5p gaTGCTGCTtccatt CAGCAGCA m7b (m7b->m6b) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-4261 gatgcTGTTTCCatt AGGAAACA m7b Created HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-497-5p gaTGCTGCTtccatt CAGCAGCA m7b (m7b->m6b) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6079 gatgctGCTTCCAtt UUGGAAGC m7b Disrupted HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-671-5p gatgctGCTTCCatt AGGAAGCC m6b Disrupted HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6828-5p gatgcTGCTTCCatt AGGAAGCA m7b Disrupted HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6838-5p gaTGCTGCTTccatt AAGCAGCA m8a Disrupted HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-103a-3p gATGCTGCTtccatt AGCAGCAU m8a (m8a->m7a) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-107 gATGCTGCTtccatt AGCAGCAU m8a (m8a->m7a) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-15a-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-15b-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-16-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-195-5p gaTGCTGCTtccatt UAGCAGCA m7b (m7b->m6b) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-3688-3p gatgctgTTTCCATt UAUGGAAA m7b Created HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-424-5p gaTGCTGCTtccatt CAGCAGCA m7b (m7b->m6b) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-4261 gatgcTGTTTCCatt AGGAAACA m7b Created HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-497-5p gaTGCTGCTtccatt CAGCAGCA m7b (m7b->m6b) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6079 gatgctGCTTCCAtt UUGGAAGC m7b Disrupted HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-671-5p gatgctGCTTCCatt AGGAAGCC m6b Disrupted HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6828-5p gatgcTGCTTCCatt AGGAAGCA m7b Disrupted HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6838-5p gaTGCTGCTTccatt AAGCAGCA m8a Disrupted HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909

Mutation Mutation ID Sample Name Cancer Type
chr6:g.104785182C>T COSM4689442 T3080 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6079 ctGCTTCCAttcctc UUGGAAGC m7b (m7b->m6b) HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-671-5p ctGCTTCCattcctc AGGAAGCC m6b Disrupted HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6828-5p cTGCTTCCattcctc AGGAAGCA m7b Disrupted HHHNE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6079 ctGCTTCCAttcctc UUGGAAGC m7b (m7b->m6b) HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-671-5p ctGCTTCCattcctc AGGAAGCC m6b Disrupted HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909
hsa-miR-6828-5p cTGCTTCCattcctc AGGAAGCA m7b Disrupted HHHSE_7550_HACE1|NM_020771|exon_CDS|-6.8138744615332|1.36893630214909

*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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