chr6:31236526:> Detail (hg19) (HLA-C)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr6:31,236,526-31,239,869 |
| hg38 | chr6:31,268,749-31,272,092 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
| Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
|---|---|---|---|---|---|---|---|---|---|
| colorectal cancer | Therapeutic Tumor Infiltrating Lymphocytes | C |
Predictive
|
Supports
|
Resistance | Somatic | 3 | 27959684 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| A patient with metastatic colorectal cancer was enrolled in a phase 2 clinical trial (NCT01174121). ... | CIViC Evidence | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg19
- Position
- chr6:31,236,526-31,239,869
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- COPY-NEUTRAL LOSS OF HETEROZYGOSITY
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/821
Genome browser