Variant #0000470931 (NC_000001.10:g.98039419C>T, NM_000110.3:c.1236G>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.98039419C>T |
DNA change (hg38) |
g.97573863C>T |
Published as |
E412E |
ISCN |
- |
DB-ID |
DPYD_000019 See all 12 reported entries |
Variant remarks |
DPD enzyme activity 0.80 (large variation); for carriers suggested initial fluoropyrimidine drug dose reduction by 0.5050%, followed by close monitoring and individual dose titration |
Reference |
PubMed: Henricks 2018 |
ClinVar ID |
- |
dbSNP ID |
rs56038477 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.01424 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2019-03-23 15:35:49 +01:00 (CET) |
Date last edited |
2020-06-11 12:18:45 +02:00 (CEST) |

Variant on transcripts
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