TRG-AS1 T cell receptor gamma locus antisense RNA 1
Information
- Symbol
- TRG-AS1
- Type
- ncRNA
- Description
- T cell receptor gamma locus antisense RNA 1
- Entrez Gene ID
- 100506776
- Genome
- hg19
- Position
- chr7:38,389,620-38,418,228
- Genome
- hg38
- Position
- chr7:38,350,019-38,378,627
- HGNC
- HGNC:48974 HGNC
- Ensembl
- ENSG00000281103 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000689202.1 | hg38 | chr7 | 38,331,119 | 38,350,558 | 19,440 |
| ENST00000702793.1 | hg38 | chr7 | 38,341,701 | 38,373,585 | 31,885 |
| ENST00000669822.2 | hg38 | chr7 | 38,341,615 | 38,373,589 | 31,975 |
| ENST00000668633.1 | hg38 | chr7 | 38,345,632 | 38,352,968 | 7,337 |
| ENST00000661780.1 | hg38 | chr7 | 38,350,019 | 38,378,627 | 28,609 |
| ENST00000689202.1 | hg19 | chr7 | 38,370,720 | 38,390,159 | 19,440 |
| ENST00000669822.2 | hg19 | chr7 | 38,381,216 | 38,413,190 | 31,975 |
| ENST00000661780.1 | hg19 | chr7 | 38,389,620 | 38,418,228 | 28,609 |
| ENST00000668633.1 | hg19 | chr7 | 38,385,233 | 38,392,569 | 7,337 |
| ENST00000702793.1 | hg19 | chr7 | 38,381,302 | 38,413,186 | 31,885 |
Genome browser