SomamiR DB 2.0 Somatic mutations altering microRNA-ceRNA interactions |
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Transcript ID: | NM_001079880 |
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Gene Symbol: | PRKD2 |
Browse Associations |
Mutation | Mutation ID | Sample Name | Cancer Type | ||
---|---|---|---|---|---|
chr19:g.46716320G>T | COSM712226 | TCGA-22-5477-01 | [lung][NS][carcinoma][squamous_cell_carcinoma] | ||
miRNA Targets Table | |||||
miR ID | miRSite | miRSeed | SeedClass | FuncClass | Cluster ID |
hsa-miR-1538 | CCGGGCCGgggtctc | CGGCCCGG | m8a | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4707-5p | ccggGCCGGGGtctc | GCCCCGGC | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4747-3p | cCGGGCCTgggtctc | AAGGCCCG | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-1538 | CCGGGCCGgggtctc | CGGCCCGG | m8a | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4707-5p | ccggGCCGGGGtctc | GCCCCGGC | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4747-3p | cCGGGCCTgggtctc | AAGGCCCG | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
Mutation | Mutation ID | Sample Name | Cancer Type | ||
---|---|---|---|---|---|
chr19:g.46716313C>T | COSM3105652 | KM12 | [large_intestine][NS][carcinoma][adenocarcinoma] | ||
miRNA Targets Table | |||||
miR ID | miRSite | miRSeed | SeedClass | FuncClass | Cluster ID |
hsa-miR-1253 | ggggTCTTCTCcgcc | AGAGAAGA | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-3150b-3p | ggggTCTCCTCcgcc | UGAGGAGA | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-3667-5p | gGGGTCTTctccgcc | AAAGACCC | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4434 | ggggtCTTCTCCgcc | AGGAGAAG | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4516 | ggggtCTTCTCCgcc | GGGAGAAG | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4784 | ggggTCTCCTCcgcc | UGAGGAGA | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-5703 | ggggtCTTCTCCgcc | AGGAGAAG | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-658 | ggggtctCCTCCGCc | GGCGGAGG | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-765 | ggggtCTCCTCCgcc | UGGAGGAG | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-1253 | ggggTCTTCTCcgcc | AGAGAAGA | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-3150b-3p | ggggTCTCCTCcgcc | UGAGGAGA | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-3667-5p | gGGGTCTTctccgcc | AAAGACCC | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4434 | ggggtCTTCTCCgcc | AGGAGAAG | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4516 | ggggtCTTCTCCgcc | GGGAGAAG | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4784 | ggggTCTCCTCcgcc | UGAGGAGA | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-5703 | ggggtCTTCTCCgcc | AGGAGAAG | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-658 | ggggtctCCTCCGCc | GGCGGAGG | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-765 | ggggtCTCCTCCgcc | UGGAGGAG | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
Mutation | Mutation ID | Sample Name | Cancer Type | ||
---|---|---|---|---|---|
chr19:g.46716312C>T | COSM3536196 | TCGA-EE-A2MT-06 | [skin][NS][malignant_melanoma][NS] | ||
miRNA Targets Table | |||||
miR ID | miRSite | miRSeed | SeedClass | FuncClass | Cluster ID |
hsa-miR-25-5p | gggtctcCTCCGCCc | AGGCGGAG | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-3150b-3p | gggTCTCCTCcgccc | UGAGGAGA | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4784 | gggTCTCCTCcgccc | UGAGGAGA | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-6077 | gggtCTCTTCCgccc | GGGAAGAG | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-658 | gggtctCCTCCGCCc | GGCGGAGG | m8a | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-765 | gggtCTCCTCCgccc | UGGAGGAG | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-25-5p | gggtctcCTCCGCCc | AGGCGGAG | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-3150b-3p | gggTCTCCTCcgccc | UGAGGAGA | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4784 | gggTCTCCTCcgccc | UGAGGAGA | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-6077 | gggtCTCTTCCgccc | GGGAAGAG | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-658 | gggtctCCTCCGCCc | GGCGGAGG | m8a | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-765 | gggtCTCCTCCgccc | UGGAGGAG | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
Mutation | Mutation ID | Sample Name | Cancer Type | ||
---|---|---|---|---|---|
chr19:g.46716301G>CG | COSM297453 | TCGA-AA-3975-01 | [large_intestine][colon][carcinoma][adenocarcinoma] | ||
miRNA Targets Table | |||||
miR ID | miRSite | miRSeed | SeedClass | FuncClass | Cluster ID |
hsa-miR-328-5p | GCCCCCCCggcggcct | GGGGGGGC | m8a | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-328-5p | GCCCCCCCggcggcct | GGGGGGGC | m8a | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
Mutation | Mutation ID | Sample Name | Cancer Type | ||
---|---|---|---|---|---|
chr19:g.46716289C>T | COSM4793510 | CHC313T | [liver][NS][carcinoma][hepatocellular_carcinoma] | ||
miRNA Targets Table | |||||
miR ID | miRSite | miRSeed | SeedClass | FuncClass | Cluster ID |
hsa-miR-1184 | cctagaGCTGCAGtc | CCUGCAGC | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-1301-3p | cctagAGCTGCAgtc | UUGCAGCU | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4418 | cctagagCTGCAGTc | CACUGCAG | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4660 | cctaGAGCTGCAgtc | UGCAGCUC | m8a | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4772-3p | cctagaGTTGCAGtc | CCUGCAAC | m7b | Created | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-5047 | cctagAGCTGCAgtc | UUGCAGCU | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-509-3-5p | cctagagCTGCAGTc | UACUGCAG | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-509-5p | cctagagCTGCAGTc | UACUGCAG | m7b | Disrupted | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-5684 | cCTAGAGTTgcagtc | AACUCUAG | m8a | (m7a->m8a) | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-618 | ccTAGAGTTgcagtc | AAACUCUA | m7b | (m6b->m7b) | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-6502-5p | cCTAGAGCTgcagtc | AGCUCUAG | m8a | (m8a->m7a) | HHHNA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-1184 | cctagaGCTGCAGtc | CCUGCAGC | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-1301-3p | cctagAGCTGCAgtc | UUGCAGCU | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4418 | cctagagCTGCAGTc | CACUGCAG | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4660 | cctaGAGCTGCAgtc | UGCAGCUC | m8a | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-4772-3p | cctagaGTTGCAGtc | CCUGCAAC | m7b | Created | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-5047 | cctagAGCTGCAgtc | UUGCAGCU | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-509-3-5p | cctagagCTGCAGTc | UACUGCAG | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-509-5p | cctagagCTGCAGTc | UACUGCAG | m7b | Disrupted | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-5684 | cCTAGAGTTgcagtc | AACUCUAG | m8a | (m7a->m8a) | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-618 | ccTAGAGTTgcagtc | AAACUCUA | m7b | (m6b->m7b) | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |
hsa-miR-6502-5p | cCTAGAGCTgcagtc | AGCUCUAG | m8a | (m8a->m7a) | HHHSA_12677_PRKD2|NM_001079880|exon_utr5|-3.91015746034921|1.63667562424729 |