chr4:152324294:> Detail (hg38) (FBXW7)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr4:153,245,446-153,332,714 |
| hg38 | chr4:152,324,294-152,411,562 |
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 |
|---|---|---|
| 418 patients with advanced cancer were screened for FBXW7 mutations using a multiplex gene panel. 17... | CIViC Evidence | Detail |
| 65 patients were retrospectively analyzed for mutational profiles predictive of response to EGFR-inh... | 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
- hg38
- Position
- chr4:152,324,294-152,411,562
- Variant Type
- snv
- Transcript 1 (CIViC Variant)
- ENST00000281708.4
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/281
- Variant (CIViC) (CIViC Variant)
- MUTATION
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