Variant #0000037549 (NC_000001.10:g.97564154C>T, NM_000110.3:c.2657G>A (DPYD))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.97564154C>T
DNA change (hg38) g.97098598C>T
Published as -
ISCN -
DB-ID DPYD_000000 See all 16 reported entries
Variant remarks expression cloning no detecable DPD activity
Reference PubMed: Vreken 1997
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-06-19 22:38:21 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
DPYD NM_000110.3 +/. 21 c.2657G>A r.(?) p.Arg886His -


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