chr8:68939529:> Detail (hg19) (PREX2)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr8:68,939,529-68,939,531 |
| hg38 | chr8:68,027,294-68,027,296 |
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
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| In a retrospective study of 44 relapsed melanoma patients harboring BRAF V600E/K (known BRAF inhibit... | 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
- chr8:68,939,529-68,939,531
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- R172I
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/2364
Genome browser