INTS15 integrator complex subunit 15
Information
- Symbol
- INTS15
- Type
- protein-coding
- Description
- integrator complex subunit 15
- Entrez Gene ID
- 79034
- Genome
- hg19
- Position
- chr7:6,629,652-6,648,357
- Genome
- hg38
- Position
- chr7:6,590,021-6,608,726
- HGNC
- HGNC:21702 HGNC
- Ensembl
- ENSG00000146576 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
18 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C7orf26 |
| HGNC | HGNC:21702 HGNC |
| Ensembl | ENSG00000146576 Ensembl |
| AllianceGenome | HGNC:21702 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000359073.9 | hg38 | chr7 | 6,590,144 | 6,608,724 | 18,581 |
| ENST00000344417.10 | hg38 | chr7 | 6,590,021 | 6,608,726 | 18,706 |
| ENST00000344417.10 | hg19 | chr7 | 6,629,652 | 6,648,357 | 18,706 |
| ENST00000359073.9 | hg19 | chr7 | 6,629,775 | 6,648,355 | 18,581 |
Genome browser