TRGV8 T cell receptor gamma variable 8
Information
- Symbol
- TRGV8
- Type
- other
- Description
- T cell receptor gamma variable 8
- Entrez Gene ID
- 6982
- Genome
- hg19
- Position
- chr7:38,369,944-38,370,536
- Genome
- hg38
- Position
- chr7:38,330,343-38,330,935
- HGNC
- HGNC:12294 HGNC
- Ensembl
- ENSG00000211696 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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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
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MGeND data only
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
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MGeND data only
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| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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 | TCRGV8 |
| SYNONYM | V1S8 |
| HGNC | HGNC:12294 HGNC |
| Ensembl | ENSG00000211696 Ensembl |
| IMGT/GENE-DB | TRGV8 |
| AllianceGenome | HGNC:12294 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000390343.2 | hg38 | chr7 | 38,330,343 | 38,330,935 | 593 |
| ENST00000390343.2 | hg19 | chr7 | 38,369,944 | 38,370,536 | 593 |
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