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 25 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 International |
| 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) |

Variant on transcripts
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