Variant #0000470933 (NC_000001.10:g.97915614C>T, NC_000001.10(NM_000110.3):c.1905+1G>A (DPYD))

Chromosome 1
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign (!)
DNA change (genomic) (Relative to hg19 / GRCh37) g.97915614C>T
DNA change (hg38) g.97450058C>T
Published as -
ISCN -
DB-ID DPYD_000006 See all 24 reported entries
Variant remarks DPD enzyme activity 0.55; for carriers suggested initial fluoropyrimidine drug dose reduction by 0.50
Reference PubMed: Henricks 2018
ClinVar ID -
dbSNP ID rs3918290
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00574 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 2019-03-23 15:45:38 +01:00 (CET)
Date last edited 2020-06-11 12:18:45 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
DPYD NM_000110.3 +/. 14i c.1905+1G>A r.spl p.? DPYD*2A


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.