PDGFRA AMPLIFICATION Detail (hg38) (PDGFRA)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr4:55,095,264-55,164,414 View the variant detail on this assembly version. |
hg38 | chr4:54,229,097-54,298,247 |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
---|---|---|---|---|---|---|---|---|---|
lung non-small cell carcinoma | Sunitinib | D |
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Sensitivity/Response | Somatic | 3 | 19366796 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
In the sunitinib-sensitive adenosquamous NSCLC cell line, PDGFRA expression was associated with foca... | 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
- PDGFRA
- Genome
- hg38
- Position
- chr4:54,229,097-54,298,247
- Variant Type
- cnv
- Variant (CIViC) (CIViC Variant)
- AMPLIFICATION
- Transcript 1 (CIViC Variant)
- ENST00000257290.5
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/716
Genome browser