DPYD EXON 11-19 DELETION Detail (hg38) (DPYD)

Information

Genome

Assembly Position
hg19 chr1:97,700,408-98,039,526 View the variant detail on this assembly version.
hg38 chr1:97,234,852-97,573,970
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 612779 OMIM
HGNC 3012 HGNC
Ensembl ENSG00000188641 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
head and neck squamous cell carcinoma Leucovorin,Fluorouracil C Predictive Supports Sensitivity/Response Somatic 4 31871216 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
A 69 year old patient diagnosed with HNSCC presented with an unresectable neck mass three months aft... 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
DPYD
Genome
hg38
Position
chr1:97,234,852-97,573,970
Variant Type
cnv
Variant (CIViC) (CIViC Variant)
EXON 11-19 DELETION
Transcript 1 (CIViC Variant)
ENST00000370192.3
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/2893
Genome browser