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_0058422
Gene Symbol: EPHA4
Browse Associations
Browse Pathways

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr2:g.221443553C>T COSM3695298 TCGA-AZ-4615-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-106b-3p agCAGTGCGagagtt CCGCACUG m7b (m7b->m6b) HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-216b-3p agcAGTGTGagagtt ACACACUU m6b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-342-3p agcaGTGTGAGAgtt UCUCACAC m8a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6814-3p agcagTGCGAGagtt ACUCGCAU m6b Disrupted HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-106b-3p agCAGTGCGagagtt CCGCACUG m7b (m7b->m6b) HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-216b-3p agcAGTGTGagagtt ACACACUU m6b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-342-3p agcaGTGTGAGAgtt UCUCACAC m8a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6814-3p agcagTGCGAGagtt ACUCGCAU m6b Disrupted HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-106b-3p agCAGTGCGagagtt CCGCACUG m7b (m7b->m6b) HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-216b-3p agcAGTGTGagagtt ACACACUU m6b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-342-3p agcaGTGTGAGAgtt UCUCACAC m8a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6814-3p agcagTGCGAGagtt ACUCGCAU m6b Disrupted HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-106b-3p agCAGTGCGagagtt CCGCACUG m7b (m7b->m6b) HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-216b-3p agcAGTGTGagagtt ACACACUU m6b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-342-3p agcaGTGTGAGAgtt UCUCACAC m8a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6814-3p agcagTGCGAGagtt ACUCGCAU m6b Disrupted HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
Mutation Mutation ID Sample Name Cancer Type
chr2:g.221443530C>G COSM3909679 TCGA-ER-A2NE-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr2:g.221443529G>A COSM4091838 TCGA-CG-4306-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1265 aattgacACATCCTg CAGGAUGU m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4764-5p aattgaCACATCCtg UGGAUGUG m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-592 aatTGACACAtcctg UUGUGUCA m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-1265 aattgacACATCCTg CAGGAUGU m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4764-5p aattgaCACATCCtg UGGAUGUG m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-592 aatTGACACAtcctg UUGUGUCA m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-1265 aattgacACATCCTg CAGGAUGU m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4764-5p aattgaCACATCCtg UGGAUGUG m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-592 aatTGACACAtcctg UUGUGUCA m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-1265 aattgacACATCCTg CAGGAUGU m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4764-5p aattgaCACATCCtg UGGAUGUG m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-592 aatTGACACAtcctg UUGUGUCA m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221443519T>G COSM4957066 CHC2362T [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-5700 tccTGCATTAagatt UAAUGCAU m7a Disrupted HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6807-3p tccTGCAGTaagatt CACUGCAU m6b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-17-3p tcCTGCAGTaagatt ACUGCAGU m7a (m6a->m7a) HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200a-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200b-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-217 tccTGCAGTAagatt UACUGCAU m7a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4418 tcCTGCAGTaagatt CACUGCAG m7b (m6b->m7b) HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-3-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-5700 tccTGCATTAagatt UAAUGCAU m7a Disrupted HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6807-3p tccTGCAGTaagatt CACUGCAU m6b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-17-3p tcCTGCAGTaagatt ACUGCAGU m7a (m6a->m7a) HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200a-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200b-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-217 tccTGCAGTAagatt UACUGCAU m7a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4418 tcCTGCAGTaagatt CACUGCAG m7b (m6b->m7b) HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-3-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-5700 tccTGCATTAagatt UAAUGCAU m7a Disrupted HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6807-3p tccTGCAGTaagatt CACUGCAU m6b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-17-3p tcCTGCAGTaagatt ACUGCAGU m7a (m6a->m7a) HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200a-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200b-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-217 tccTGCAGTAagatt UACUGCAU m7a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4418 tcCTGCAGTaagatt CACUGCAG m7b (m6b->m7b) HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-3-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-5700 tccTGCATTAagatt UAAUGCAU m7a Disrupted HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-6807-3p tccTGCAGTaagatt CACUGCAU m6b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-17-3p tcCTGCAGTaagatt ACUGCAGU m7a (m6a->m7a) HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200a-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-200b-5p tcctgcaGTAAGATt CAUCUUAC m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-217 tccTGCAGTAagatt UACUGCAU m7a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-4418 tcCTGCAGTaagatt CACUGCAG m7b (m6b->m7b) HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-3-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-509-5p tcCTGCAGTAagatt UACUGCAG m8a Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
Mutation Mutation ID Sample Name Cancer Type
chr2:g.221443506A>G COSM4418893 SNUH_G76_S1 [haematopoietic_and_lymphoid_tissue][NS][haematopoietic_neoplasm][acute_myeloid_leukaemia]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr2:g.221443503T>C COSM3838704 TCGA-A8-A09Z-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-202-5p aaaaagtCATAGGAg UUCCUAUG m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-337-3p aaaaagtTATAGGAg CUCCUAUA m7b Disrupted HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-202-5p aaaaagtCATAGGAg UUCCUAUG m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-337-3p aaaaagtTATAGGAg CUCCUAUA m7b Disrupted HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-202-5p aaaaagtCATAGGAg UUCCUAUG m7b Created HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-337-3p aaaaagtTATAGGAg CUCCUAUA m7b Disrupted HHHNE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-202-5p aaaaagtCATAGGAg UUCCUAUG m7b Created HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872
hsa-miR-337-3p aaaaagtTATAGGAg CUCCUAUA m7b Disrupted HHHSE_5773_EPHA4|NM_004438|exon_CDS|-5.48462456603386|-1.37711163508872

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221442911G>T COSM573754 TCGA-50-5068-01 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3664-5p aACAGAGTagagact AACUCUGU m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4684-5p aacagaGTAGAGAct CUCUCUAC m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4714-5p aaCAGAGTagagact AACUCUGA m6b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3664-5p aACAGAGTagagact AACUCUGU m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4684-5p aacagaGTAGAGAct CUCUCUAC m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4714-5p aaCAGAGTagagact AACUCUGA m6b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3664-5p aACAGAGTagagact AACUCUGU m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4684-5p aacagaGTAGAGAct CUCUCUAC m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4714-5p aaCAGAGTagagact AACUCUGA m6b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3664-5p aACAGAGTagagact AACUCUGU m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4684-5p aacagaGTAGAGAct CUCUCUAC m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4714-5p aaCAGAGTagagact AACUCUGA m6b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221442911G>A COSM4904712 TCGA-BF-A3DL-01 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1236-3p aacagaGAAGAGact CCUCUUCC m6b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6809-3p aacAGAGAAGagact CUUCUCUU m7a Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-942-5p aacAGAGAAGAgact UCUUCUCU m8a Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-1236-3p aacagaGAAGAGact CCUCUUCC m6b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6809-3p aacAGAGAAGagact CUUCUCUU m7a Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-942-5p aacAGAGAAGAgact UCUUCUCU m8a Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-1236-3p aacagaGAAGAGact CCUCUUCC m6b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6809-3p aacAGAGAAGagact CUUCUCUU m7a Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-942-5p aacAGAGAAGAgact UCUUCUCU m8a Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-1236-3p aacagaGAAGAGact CCUCUUCC m6b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4279 aacaGAGGAGAGact CUCUCCUC m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6780a-3p aaCAGAGGAGagact CUCCUCUG m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6809-3p aacAGAGAAGagact CUUCUCUU m7a Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6845-3p aacagAGGAGAGact CCUCUCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6895-3p aacagagGAGAGACt UGUCUCUC m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-942-5p aacAGAGAAGAgact UCUUCUCU m8a Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221442902C>T COSM3578162 TCGA-EE-A3AE-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3184-3p GAGACTTTctgagtg AAAGUCUC m8a Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3664-3p gagactTCCTGAGtg UCUCAGGA m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4476 gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-510-5p gagacttCCTGAGTg UACUCAGG m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6876-5p gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-873-5p gagacTTCCTGagtg GCAGGAAC m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3184-3p GAGACTTTctgagtg AAAGUCUC m8a Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3664-3p gagactTCCTGAGtg UCUCAGGA m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4476 gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-510-5p gagacttCCTGAGTg UACUCAGG m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6876-5p gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-873-5p gagacTTCCTGagtg GCAGGAAC m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3184-3p GAGACTTTctgagtg AAAGUCUC m8a Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3664-3p gagactTCCTGAGtg UCUCAGGA m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4476 gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-510-5p gagacttCCTGAGTg UACUCAGG m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6876-5p gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-873-5p gagacTTCCTGagtg GCAGGAAC m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3184-3p GAGACTTTctgagtg AAAGUCUC m8a Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3664-3p gagactTCCTGAGtg UCUCAGGA m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4476 gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-510-5p gagacttCCTGAGTg UACUCAGG m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6876-5p gagaCTTCCTGagtg CAGGAAGG m7a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-873-5p gagacTTCCTGagtg GCAGGAAC m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221442894A>G COSM1405748 TCGA-AA-3713-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4286 ctgAGTGGGGccagc ACCCCACU m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4757-5p ctgagtGAGGCCagc AGGCCUCU m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4758-3p ctgaGTGGGGCcagc UGCCCCAC m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6744-3p ctgagtGAGGCCagc GGGCCUCU m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6878-3p ctgagtGAGGCCAGc CUGGCCUC m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-874-5p ctgagTGGGGCCagc CGGCCCCA m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3176 ctgagtgAGGCCAGc ACUGGCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3922-3p ctgagtgAGGCCAGc UCUGGCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4286 ctgAGTGGGGccagc ACCCCACU m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4757-5p ctgagtGAGGCCagc AGGCCUCU m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4758-3p ctgaGTGGGGCcagc UGCCCCAC m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6744-3p ctgagtGAGGCCagc GGGCCUCU m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6878-3p ctgagtGAGGCCAGc CUGGCCUC m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-874-5p ctgagTGGGGCCagc CGGCCCCA m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3176 ctgagtgAGGCCAGc ACUGGCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3922-3p ctgagtgAGGCCAGc UCUGGCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4286 ctgAGTGGGGccagc ACCCCACU m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4757-5p ctgagtGAGGCCagc AGGCCUCU m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4758-3p ctgaGTGGGGCcagc UGCCCCAC m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6744-3p ctgagtGAGGCCagc GGGCCUCU m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6878-3p ctgagtGAGGCCAGc CUGGCCUC m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-874-5p ctgagTGGGGCCagc CGGCCCCA m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3176 ctgagtgAGGCCAGc ACUGGCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3922-3p ctgagtgAGGCCAGc UCUGGCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4286 ctgAGTGGGGccagc ACCCCACU m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4757-5p ctgagtGAGGCCagc AGGCCUCU m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4758-3p ctgaGTGGGGCcagc UGCCCCAC m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6744-3p ctgagtGAGGCCagc GGGCCUCU m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6878-3p ctgagtGAGGCCAGc CUGGCCUC m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-874-5p ctgagTGGGGCCagc CGGCCCCA m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3176 ctgagtgAGGCCAGc ACUGGCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3922-3p ctgagtgAGGCCAGc UCUGGCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221442893G>T COSM48332 16921 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3176 tgagtgAGGCCAGca ACUGGCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3922-3p tgagtgAGGCCAGca UCUGGCCU m7b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4642 tgagtGATGCCAgca AUGGCAUC m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4720-5p tgagtgATGCCAGca CCUGGCAU m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4757-5p tgagtGAGGCCagca AGGCCUCU m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4799-3p tgagtgATGCCAGca ACUGGCAU m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-5588-5p tgagtgATGCCAGca ACUGGCAU m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6744-3p tgagtGAGGCCagca GGGCCUCU m6b Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6878-3p tgagtGAGGCCAGca CUGGCCUC m8a Disrupted HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-7112-3p tgaGTGATGCcagca UGCAUCAC m7b Created HHHNE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3176 tgagtgAGGCCAGca ACUGGCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-3922-3p tgagtgAGGCCAGca UCUGGCCU m7b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4642 tgagtGATGCCAgca AUGGCAUC m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4720-5p tgagtgATGCCAGca CCUGGCAU m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4757-5p tgagtGAGGCCagca AGGCCUCU m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-4799-3p tgagtgATGCCAGca ACUGGCAU m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-5588-5p tgagtgATGCCAGca ACUGGCAU m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6744-3p tgagtGAGGCCagca GGGCCUCU m6b Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-6878-3p tgagtGAGGCCAGca CUGGCCUC m8a Disrupted HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589
hsa-miR-7112-3p tgaGTGATGCcagca UGCAUCAC m7b Created HHHSE_5772_EPHA4|NM_004438|exon_CDS|-6.05475618844164|1.22724209317589

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221434182C>T COSM1016966 TCGA-AX-A05Z-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3529-3p gtgaTGTTGTacggg AACAACAA m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3678-5p gtgatgtTGTACGGg UCCGUACA m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3913-3p gTGATGTCgtacggg AGACAUCA m7b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3529-3p gtgaTGTTGTacggg AACAACAA m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3678-5p gtgatgtTGTACGGg UCCGUACA m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3913-3p gTGATGTCgtacggg AGACAUCA m7b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3529-3p gtgaTGTTGTacggg AACAACAA m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3678-5p gtgatgtTGTACGGg UCCGUACA m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3913-3p gTGATGTCgtacggg AGACAUCA m7b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3529-3p gtgaTGTTGTacggg AACAACAA m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3678-5p gtgatgtTGTACGGg UCCGUACA m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3913-3p gTGATGTCgtacggg AGACAUCA m7b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221434177G>T COSM573761 TCGA-50-6592-01 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2116-3p gtcgtacTGGGAGag CCUCCCAU m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4712-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4713-5p gtcgtacTGGGAGAg UUCUCCCA m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-532-3p gtcgtacTGGGAGag CCUCCCAC m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-770-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-2116-3p gtcgtacTGGGAGag CCUCCCAU m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4712-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4713-5p gtcgtacTGGGAGAg UUCUCCCA m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-532-3p gtcgtacTGGGAGag CCUCCCAC m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-770-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-2116-3p gtcgtacTGGGAGag CCUCCCAU m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4712-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4713-5p gtcgtacTGGGAGAg UUCUCCCA m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-532-3p gtcgtacTGGGAGag CCUCCCAC m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-770-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-2116-3p gtcgtacTGGGAGag CCUCCCAU m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4712-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4713-5p gtcgtacTGGGAGAg UUCUCCCA m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-532-3p gtcgtacTGGGAGag CCUCCCAC m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-770-5p gtcGTACTGGgagag UCCAGUAC m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221434177G>A COSM1405744 TCGA-D5-6537-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4469 gtcgtacAGGGAGag GCUCCCUC m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-486-5p gtcGTACAGGgagag UCCUGUAC m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6867-3p gtcgtacAGGGAGAg CUCUCCCU m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-7113-3p gtcgtaCAGGGAGag CCUCCCUG m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4469 gtcgtacAGGGAGag GCUCCCUC m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-486-5p gtcGTACAGGgagag UCCUGUAC m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6867-3p gtcgtacAGGGAGAg CUCUCCCU m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-7113-3p gtcgtaCAGGGAGag CCUCCCUG m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4469 gtcgtacAGGGAGag GCUCCCUC m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-486-5p gtcGTACAGGgagag UCCUGUAC m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6867-3p gtcgtacAGGGAGAg CUCUCCCU m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-7113-3p gtcgtaCAGGGAGag CCUCCCUG m7b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4469 gtcgtacAGGGAGag GCUCCCUC m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-486-5p gtcGTACAGGgagag UCCUGUAC m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6763-3p gtcgtaCGGGGAGag CUCCCCGG m7a Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6867-3p gtcgtacAGGGAGAg CUCUCCCU m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-7113-3p gtcgtaCAGGGAGag CCUCCCUG m7b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221434166C>T COSM95850 86788 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1296-5p agaGGCCCTAttggg UUAGGGCC m7b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3142 agAGGCCTTattggg AAGGCCUU m7a (m6a->m7a) HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4512 agAGGCCCTattggg CAGGGCCU m7b (m7b->m6b) HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4753-5p agaGGCCTTattggg CAAGGCCA m6b Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4757-5p AGAGGCCTtattggg AGGCCUCU m8a Created HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6826-5p agaggcCCTATTGgg UCAAUAGG m7b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6895-5p agaGGCCCTattggg CAGGGCCA m6b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-7160-3p agaGGCCCTattggg CAGGGCCC m6b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-1296-5p agaGGCCCTAttggg UUAGGGCC m7b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-3142 agAGGCCTTattggg AAGGCCUU m7a (m6a->m7a) HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4512 agAGGCCCTattggg CAGGGCCU m7b (m7b->m6b) HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4753-5p agaGGCCTTattggg CAAGGCCA m6b Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4757-5p AGAGGCCTtattggg AGGCCUCU m8a Created HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6826-5p agaggcCCTATTGgg UCAAUAGG m7b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-6895-5p agaGGCCCTattggg CAGGGCCA m6b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-7160-3p agaGGCCCTattggg CAGGGCCC m6b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839

Mutation Mutation ID Sample Name Cancer Type
chr2:g.221434159G>A COSM3578152 TCGA-FS-A1ZA-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-323b-3p cTATTGGGatatgtc CCCAAUAC m7a Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4733-5p ctaTTGGGATatgtc AAUCCCAA m7b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-323b-3p cTATTGGGatatgtc CCCAAUAC m7a Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4733-5p ctaTTGGGATatgtc AAUCCCAA m7b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-323b-3p cTATTGGGatatgtc CCCAAUAC m7a Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4733-5p ctaTTGGGATatgtc AAUCCCAA m7b Disrupted HHHNE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-323b-3p cTATTGGGatatgtc CCCAAUAC m7a Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839
hsa-miR-4733-5p ctaTTGGGATatgtc AAUCCCAA m7b Disrupted HHHSE_5771_EPHA4|NM_004438|exon_CDS|-5.48546986194733|2.00885742039839

*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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