PTGS2 OVEREXPRESSION Detail (hg38) (PTGS2)

Information

Genome

Assembly Position
hg19 chr1:186,640,923-186,649,559 View the variant detail on this assembly version.
hg38 chr1:186,671,791-186,680,427
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 600262 OMIM
HGNC 9605 HGNC
Ensembl ENSG00000073756 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
colorectal cancer Aspirin B Predictive Supports Sensitivity/Response Somatic 3 17522398 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Mail-in surveys conducted every two years since 1980 evaluated 82,911 woman and 47,363 men for regul... 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
PTGS2
Genome
hg38
Position
chr1:186,671,791-186,680,427
Variant Type
cnv
Variant (CIViC) (CIViC Variant)
OVEREXPRESSION
Transcript 1 (CIViC Variant)
ENST00000367468.5
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/619
Genome browser