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_0068869
Gene Symbol: FGFR3
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Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr4:g.1799433C>T COSM4485134 CSCC-29-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-21-3p gcaGGTGTTGaatgc CAACACCA m7a Created HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-3065-3p gcaGGTGCTGAatgc UCAGCACC m8a Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-383-3p gcagGTGCTGaatgc ACAGCACU m6b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-421 gcaggTGTTGAatgc AUCAACAG m6b Created HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4272 gcaggtGTTGAATGc CAUUCAAC m8a Created HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6804-3p gCAGGTGCtgaatgc CGCACCUG m7b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6871-3p gcaGGTGCTGaatgc CAGCACCC m7a Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-21-3p gcaGGTGTTGaatgc CAACACCA m7a Created HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-3065-3p gcaGGTGCTGAatgc UCAGCACC m8a Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-383-3p gcagGTGCTGaatgc ACAGCACU m6b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-421 gcaggTGTTGAatgc AUCAACAG m6b Created HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4272 gcaggtGTTGAATGc CAUUCAAC m8a Created HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6804-3p gCAGGTGCtgaatgc CGCACCUG m7b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6871-3p gcaGGTGCTGaatgc CAGCACCC m7a Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-21-3p gcaGGTGTTGaatgc CAACACCA m7a Created HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-3065-3p gcaGGTGCTGAatgc UCAGCACC m8a Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-383-3p gcagGTGCTGaatgc ACAGCACU m6b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-421 gcaggTGTTGAatgc AUCAACAG m6b Created HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4272 gcaggtGTTGAATGc CAUUCAAC m8a Created HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6804-3p gCAGGTGCtgaatgc CGCACCUG m7b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6871-3p gcaGGTGCTGaatgc CAGCACCC m7a Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-21-3p gcaGGTGTTGaatgc CAACACCA m7a Created HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-3065-3p gcaGGTGCTGAatgc UCAGCACC m8a Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-383-3p gcagGTGCTGaatgc ACAGCACU m6b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-421 gcaggTGTTGAatgc AUCAACAG m6b Created HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4272 gcaggtGTTGAATGc CAUUCAAC m8a Created HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6804-3p gCAGGTGCtgaatgc CGCACCUG m7b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-6871-3p gcaGGTGCTGaatgc CAGCACCC m7a Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036

Mutation Mutation ID Sample Name Cancer Type
chr4:g.1799410TG>T COSM4616015 SW48 [large_intestine][NS][other][neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4733-3p gtCCTGGTGGggcccc CCACCAGG m8a Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4758-3p gtcctgGTGGGGCccc UGCCCCAC m7b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-874-5p gtcctggTGGGGCCcc CGGCCCCA m7b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4733-3p gtCCTGGTGGggcccc CCACCAGG m8a Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4758-3p gtcctgGTGGGGCccc UGCCCCAC m7b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-874-5p gtcctggTGGGGCCcc CGGCCCCA m7b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4733-3p gtCCTGGTGGggcccc CCACCAGG m8a Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4758-3p gtcctgGTGGGGCccc UGCCCCAC m7b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-874-5p gtcctggTGGGGCCcc CGGCCCCA m7b Disrupted HHHNA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4733-3p gtCCTGGTGGggcccc CCACCAGG m8a Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-4758-3p gtcctgGTGGGGCccc UGCCCCAC m7b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036
hsa-miR-874-5p gtcctggTGGGGCCcc CGGCCCCA m7b Disrupted HHHSA_17186_FGFR3|NM_000142|exon_CDS|-3.99324273961745|1.31411654694036

*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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