chr1:97543299:> Detail (hg19) (DPYD)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr1:97,543,299-98,386,605 |
hg38 | chr1:97,077,743-97,921,049 |
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 |
---|---|---|
The Clinical Pharmacogenomics Implementation Consortium Guidelines for DPYD genotype and 5-FU dosing... | 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
- chr1:97,543,299-98,386,605
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- RS67376798 HOMOZYGOSITY
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/740
Genome browser