List of variants reported as drug response for fluorouracil response - Other

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000110.4(DPYD):c.2194G>A (p.Val732Ile)	rs1801160	0.03794
NM_000110.4(DPYD):c.1129-5923C>G	rs75017182	0.01296
NM_000110.4(DPYD):c.557A>G (p.Tyr186Cys)	rs115232898	0.00622
NM_000110.4(DPYD):c.1905+1G>A	rs3918290	0.00474
NM_000110.4(DPYD):c.2846A>T (p.Asp949Val)	rs67376798	0.00334
NM_000110.4(DPYD):c.1679T>G (p.Ile560Ser)	rs55886062	0.00040
NM_000110.4(DPYD):c.2303C>A (p.Thr768Lys)	rs56005131	0.00011
NM_000110.4(DPYD):c.1774C>T (p.Arg592Trp)	rs59086055	0.00006
NM_000110.4(DPYD):c.1543G>A (p.Val515Ile)	rs148994843	0.00005
NM_000110.4(DPYD):c.703C>T (p.Arg235Trp)	rs1801266	0.00004
NM_000110.4(DPYD):c.1156G>T (p.Glu386Ter)	rs78060119	0.00001
NM_000110.4(DPYD):c.1003G>T (p.Val335Leu)	rs72549306
NM_000110.4(DPYD):c.1898del (p.Pro633fs)	rs72549303
NM_000110.4(DPYD):c.2983G>T (p.Val995Phe)	rs1801268

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.