Mutation
|
Mutation ID
|
Sample Name
|
Cancer Type
|
chr6:g.31636602C>T
|
COSM3624635
|
TCGA-D9-A149-06
|
[skin][NS][malignant_melanoma][NS]
|
miRNA Targets Table
|
miR ID |
miRSite |
miRSeed |
SeedClass |
FuncClass |
Cluster ID |
hsa-miR-1285-3p |
ctccTGCCCAGcagg |
UCUGGGCA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-3187-5p |
ctccTGCCCAGcagg |
CCUGGGCA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-3692-5p |
ctcctgcCCAGCAGg |
CCUGCUGG |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-4468 |
ctcCTGCTCagcagg |
AGAGCAGA |
m6b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-4486 |
ctcctGCCCAGCagg |
GCUGGGCG |
m7a |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-4663 |
ctcctGCTCAGCagg |
AGCUGAGC |
m7b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-4690-5p |
ctCCTGCTCagcagg |
GAGCAGGC |
m7a |
(m6a->m7a) |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-4722-5p |
CTCCTGCCcagcagg |
GGCAGGAG |
m8a |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-5189-5p |
ctccTGCCCAGcagg |
UCUGGGCA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-5589-5p |
ctcctgCCCAGCagg |
GGCUGGGU |
m6b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-612 |
ctccTGCCCAGCagg |
GCUGGGCA |
m8a |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-6165 |
cTCCTGCTcagcagg |
CAGCAGGA |
m7b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-6721-5p |
ctCCTGCCCAgcagg |
UGGGCAGG |
m8a |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-6860 |
ctccTGCCCAGcagg |
ACUGGGCA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-8077 |
ctcctgCTCAGCagg |
GGCUGAGU |
m6b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-93-3p |
ctcctgcTCAGCAGg |
ACUGCUGA |
m7b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
Mutation
|
Mutation ID
|
Sample Name
|
Cancer Type
|
chr6:g.31636555C>T
|
COSM4160841
|
PTC-7C
|
[thyroid][NS][other][neoplasm]
|
miRNA Targets Table
|
miR ID |
miRSite |
miRSeed |
SeedClass |
FuncClass |
Cluster ID |
hsa-miR-2467-3p |
tactCCTCTGCagcc |
AGCAGAGG |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-3158-5p |
tactccTCTGCAGcc |
CCUGCAGA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-3678-3p |
tactcCTCTGCAGcc |
CUGCAGAG |
m8a |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-518a-5p |
tactcCTTTGCAGcc |
CUGCAAAG |
m8a |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-527 |
tactcCTTTGCAGcc |
CUGCAAAG |
m8a |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-6847-5p |
tacTCCTCTGcagcc |
ACAGAGGA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
Mutation
|
Mutation ID
|
Sample Name
|
Cancer Type
|
chr6:g.31636554T>A
|
COSM4160840
|
PTC-7C
|
[thyroid][NS][other][neoplasm]
|
miRNA Targets Table
|
miR ID |
miRSite |
miRSeed |
SeedClass |
FuncClass |
Cluster ID |
hsa-miR-17-3p |
ctactccACTGCAGc |
ACUGCAGU |
m7b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-2467-3p |
ctactCCTCTGCagc |
AGCAGAGG |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-3158-5p |
ctactccTCTGCAGc |
CCUGCAGA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-3678-3p |
ctactcCTCTGCAGc |
CUGCAGAG |
m8a |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-5693 |
ctactCCACTGCagc |
GCAGUGGC |
m7a |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-6499-3p |
ctactcCACTGCagc |
AGCAGUGU |
m6b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-6847-5p |
ctacTCCTCTGcagc |
ACAGAGGA |
m7b |
Disrupted |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
Mutation
|
Mutation ID
|
Sample Name
|
Cancer Type
|
chr6:g.31636550C>T
|
COSM4160839
|
PTC-7C
|
[thyroid][NS][other][neoplasm]
|
miRNA Targets Table
|
miR ID |
miRSite |
miRSeed |
SeedClass |
FuncClass |
Cluster ID |
hsa-miR-3125 |
tattctaTTCCTCTg |
UAGAGGAA |
m7b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-3916 |
tattctaTTCCTCTg |
AAGAGGAA |
m7b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
hsa-miR-6859-5p |
tattctaTTCCTCTg |
GAGAGGAA |
m7b |
Created |
HHHNH_2914_PRRC2A|NM_004638-1|exon_CDS|-7.0295875659816|-0.0222128781435683 |
*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.