Variant #0000470932 (NC_000001.10:g.97981343A>C, NM_000110.3:c.1679T>G (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.97981343A>C
DNA change (hg38) g.97515787A>C
Published as -
ISCN -
DB-ID DPYD_000016 See all 8 reported entries
Variant remarks DPD enzyme activity 0.40; for carriers suggested initial fluoropyrimidine drug dose reduction by 0.50
Reference PubMed: Henricks 2018
ClinVar ID -
dbSNP ID rs55886062
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00031 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 15:41:27 +01:00 (CET)
Date last edited 2020-06-11 12:18:45 +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 +/. 13 c.1679T>G r.(?) p.(Ile560Ser) -


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