ClinVar Miner

List of variants in gene DPYS reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
NM_001385.2(DPYS):c.-154C>G rs78426610
NM_001385.3(DPYS):c.-104T>C rs541934140
NM_001385.3(DPYS):c.-1T>C rs2959023
NM_001385.3(DPYS):c.1002G>A (p.Gln334=) rs148318692
NM_001385.3(DPYS):c.1029C>G (p.Thr343=) rs117104587
NM_001385.3(DPYS):c.1062T>C (p.Asp354=) rs35013010
NM_001385.3(DPYS):c.1092+38C>T rs371343634
NM_001385.3(DPYS):c.1092+9C>T rs138453168
NM_001385.3(DPYS):c.1093-47C>A rs192507470
NM_001385.3(DPYS):c.1307T>C (p.Val436Ala) rs672601292
NM_001385.3(DPYS):c.1412A>G (p.Tyr471Cys) rs373070454
NM_001385.3(DPYS):c.1506del (p.Arg503fs) rs79080341
NM_001385.3(DPYS):c.15G>A (p.Ser5=) rs182332679
NM_001385.3(DPYS):c.19C>G (p.Leu7Val) rs57732538
NM_001385.3(DPYS):c.216C>T (p.Phe72=) rs2298840
NM_001385.3(DPYS):c.264+30G>A rs552354398
NM_001385.3(DPYS):c.264+34C>G rs189294405
NM_001385.3(DPYS):c.264+5C>T rs672601293
NM_001385.3(DPYS):c.265-58T>C rs2669429
NM_001385.3(DPYS):c.424-62G>T rs7821992
NM_001385.3(DPYS):c.541C>T (p.Arg181Trp) rs36027551
NM_001385.3(DPYS):c.765T>C (p.Ala255=) rs35371065

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.