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
Links
Type Database ID Link
Gene MIM 173490 OMIM
HGNC 8803 HGNC
Ensembl ENSG00000134853 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
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 Predictive Supports Sensitivity/Response Somatic 3 19366796 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
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
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