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_0004922
Gene Symbol: NAPG
Browse Associations

Somatic mutations that impact miRNA target sites



Mutation Mutation ID Sample Name Cancer Type
chr18:g.10548367G>A COSM1387767 TCGA-CA-6718-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3615 gtgtCCGAGAGAgct UCUCUCGG m8a Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-3687 gTGTCCGGGagagct CCCGGACA m8a (m8a->m7a) HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-3917 gtGTCCGAGagagct GCUCGGAC m7b (m6b->m7b) HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-4442 gTGTCCGGgagagct GCCGGACA m7b Disrupted HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-7110-3p gtgtccGAGAGAGct UCUCUCUC m7b Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-3615 gtgtCCGAGAGAgct UCUCUCGG m8a Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-3687 gTGTCCGGGagagct CCCGGACA m8a (m8a->m7a) HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-3917 gtGTCCGAGagagct GCUCGGAC m7b (m6b->m7b) HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-4442 gTGTCCGGgagagct GCCGGACA m7b Disrupted HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-7110-3p gtgtccGAGAGAGct UCUCUCUC m7b Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924

Mutation Mutation ID Sample Name Cancer Type
chr18:g.10548345T>C COSM4071256 TCGA-HU-8602-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-153-3p gaCTATGCAgctgca UUGCAUAG m7b (m6b->m7b) HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-221-3p gactATGTAGCTgca AGCUACAU m8a Disrupted HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-222-3p gactATGTAGCTgca AGCUACAU m8a Disrupted HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-376c-3p gaCTATGTagctgca AACAUAGA m6b Disrupted HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-5690 gactatGTAGCTGca UCAGCUAC m7b Disrupted HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-153-3p gaCTATGCAgctgca UUGCAUAG m7b (m6b->m7b) HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-221-3p gactATGTAGCTgca AGCUACAU m8a Disrupted HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-222-3p gactATGTAGCTgca AGCUACAU m8a Disrupted HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-376c-3p gaCTATGTagctgca AACAUAGA m6b Disrupted HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-5690 gactatGTAGCTGca UCAGCUAC m7b Disrupted HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924

Mutation Mutation ID Sample Name Cancer Type
chr18:g.10548333G>C COSM4580313 06-P2007 [bone][NS][Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-147a ctaCACACAaatgac GUGUGUGG m6b Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-4652-3p ctacACAGAAatgac GUUCUGUU m6b Disrupted HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-5010-3p ctacACACAAAtgac UUUUGUGU m7b Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-579-3p ctacacaCAAATGAc UUCAUUUG m7b Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-599 ctacACACAAatgac GUUGUGUC m6b Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-664b-3p ctacacaCAAATGAc UUCAUUUG m7b Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-6818-5p ctaCACACAAatgac UUGUGUGA m7a Created HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-6867-5p ctACACACAaatgac UGUGUGUG m7a (m6a->m7a) HHHNA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-147a ctaCACACAaatgac GUGUGUGG m6b Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-4652-3p ctacACAGAAatgac GUUCUGUU m6b Disrupted HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-5010-3p ctacACACAAAtgac UUUUGUGU m7b Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-579-3p ctacacaCAAATGAc UUCAUUUG m7b Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-599 ctacACACAAatgac GUUGUGUC m6b Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-664b-3p ctacacaCAAATGAc UUCAUUUG m7b Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-6818-5p ctaCACACAAatgac UUGUGUGA m7a Created HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924
hsa-miR-6867-5p ctACACACAaatgac UGUGUGUG m7a (m6a->m7a) HHHSA_11023_NAPG|NM_003826|exon_CDS|-4.79699651795927|0.357355460818924

*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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