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.