ClinVar Miner

List of variants in gene DPYD reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_000110.4(DPYD):c.681-237G>A rs2786511 0.99703
NM_000110.4(DPYD):c.2908-69A>G rs290855 0.79607
NM_000110.4(DPYD):c.2622+230G>A rs4950023 0.63891
NM_000110.4(DPYD):c.1740+40A>G rs2811178 0.61570
NM_000110.4(DPYD):c.1525-209G>A rs1337752 0.61464
NM_000110.4(DPYD):c.1975-213G>C rs6699630 0.49922
NM_000110.4(DPYD):c.2058+101T>C rs1890138 0.25652
NM_000110.4(DPYD):c.2059-94G>T rs7556439 0.23481
NM_000110.4(DPYD):c.2058+230A>G rs11582179 0.19615
NM_000110.4(DPYD):c.1906-123C>A rs56279424 0.18551
NM_000110.4(DPYD):c.1974+75A>G rs72728438 0.18528
NM_000110.4(DPYD):c.1740+39C>T rs2786783 0.17597
NM_000110.4(DPYD):c.958+134T>G rs2811202 0.15180
NM_000110.4(DPYD):c.2767-333G>A rs2171826 0.14547
NM_000110.4(DPYD):c.*274T>C rs56160474 0.14536
NM_000110.4(DPYD):c.2908-58G>C rs17116357 0.14517
NM_000110.4(DPYD):c.680+139G>A rs6668296 0.13627
NM_000110.4(DPYD):c.483+837A>G rs55684412 0.12682
NM_000110.4(DPYD):c.2058+263G>A rs55652347 0.09879
NM_000110.4(DPYD):c.763-118A>G rs3790387 0.09806
NM_000110.4(DPYD):c.2300-39G>A rs12137711 0.09021
NM_000110.4(DPYD):c.1340-106T>A rs61789183 0.08725
NM_000110.4(DPYD):c.2442+163A>G rs17432999 0.03917
NM_000110.4(DPYD):c.2194G>A (p.Val732Ile) rs1801160 0.03794
NM_000110.4(DPYD):c.1524+176G>T rs2786525 0.02721
NM_000110.4(DPYD):c.1340-181C>A rs2811162 0.02720
NM_000110.4(DPYD):c.1525-90G>A rs6657204 0.02563
NM_000110.4(DPYD):c.1218G>A (p.Met406Ile) rs61622928 0.02183
NM_000110.4(DPYD):c.1906-24A>C rs12078940 0.01855
NM_000110.4(DPYD):c.2058+264C>T rs74105115 0.01840
NM_000110.4(DPYD):c.851-31C>T rs2786491 0.01754
NM_000110.4(DPYD):c.850+41T>C rs112550271 0.01564
NM_000110.4(DPYD):c.1601G>A (p.Ser534Asn) rs1801158 0.01380
NM_000110.4(DPYD):c.483+279C>A rs79063448 0.01213
NM_000110.4(DPYD):c.2058+157G>A rs115139529 0.00747
NM_000110.4(DPYD):c.775A>G (p.Lys259Glu) rs45589337 0.00513
NM_000110.4(DPYD):c.484-145T>A rs78682297 0.00477
NM_000110.4(DPYD):c.1905+1G>A rs3918290 0.00474
NM_000110.4(DPYD):c.2908-208A>G rs76665493 0.00437
NM_000110.4(DPYD):c.1128+161G>A rs74105265 0.00414
NM_000110.4(DPYD):c.2846A>T (p.Asp949Val) rs67376798 0.00334
NM_000110.4(DPYD):c.868A>G (p.Lys290Glu) rs146356975 0.00078
NM_000110.4(DPYD):c.1679T>G (p.Ile560Ser) rs55886062 0.00040
NM_000110.4(DPYD):c.1358C>G (p.Pro453Arg) rs144395748 0.00031
NM_000110.4(DPYD):c.1229G>A (p.Arg410Gln) rs199646142 0.00012
NM_000110.4(DPYD):c.2303C>A (p.Thr768Lys) rs56005131 0.00011
NM_000110.4(DPYD):c.345G>C (p.Met115Ile) rs377169736 0.00010
NM_000110.4(DPYD):c.220C>T (p.Arg74Ter) rs189768576 0.00006
NM_000110.4(DPYD):c.2579del (p.Gln860fs) rs746991079 0.00006
NM_000110.4(DPYD):c.86G>A (p.Cys29Tyr) rs528768620 0.00006
NM_000110.4(DPYD):c.1651G>A (p.Ala551Thr) rs777425216 0.00004
NM_000110.4(DPYD):c.1681C>T (p.Arg561Ter) rs1057516968 0.00004
NM_000110.4(DPYD):c.2275C>T (p.Arg759Ter) rs759372918 0.00004
NM_000110.4(DPYD):c.257C>T (p.Pro86Leu) rs568132506 0.00004
NM_000110.4(DPYD):c.1139C>G (p.Ala380Gly) rs1354585423 0.00001
NM_000110.4(DPYD):c.1863G>A (p.Trp621Ter) rs1057516388 0.00001
NM_000110.4(DPYD):c.1974+1G>A rs772254904 0.00001
NM_000110.4(DPYD):c.2179+4A>G rs746718279 0.00001
NM_000110.4(DPYD):c.2528T>C (p.Ile843Thr) rs571114616 0.00001
NM_000110.4(DPYD):c.2767-1G>A rs377221676 0.00001
NM_000110.4(DPYD):c.61C>T (p.Arg21Ter) rs72549310 0.00001
NC_000001.11:g.97921399A>C rs61787828
NM_000110.4(DPYD):c.1243G>T (p.Glu415Ter) rs755031341
NM_000110.4(DPYD):c.1525-132dup rs141050810
NM_000110.4(DPYD):c.1740+140_1740+141insA rs56080540
NM_000110.4(DPYD):c.1740+75dup rs145228578
NM_000110.4(DPYD):c.1905+1G>C rs3918290
NM_000110.4(DPYD):c.2043_2058del (p.Leu682fs) rs773499329
NM_000110.4(DPYD):c.2058+145T>C rs1879374
NM_000110.4(DPYD):c.2075G>A (p.Arg692Gln)
NM_000110.4(DPYD):c.2135del (p.Pro712fs) rs1064796552
NM_000110.4(DPYD):c.2442+283G>A rs11808108
NM_000110.4(DPYD):c.2442+69dup rs544905665
NM_000110.4(DPYD):c.2907+55C>T rs290854
NM_000110.4(DPYD):c.2975G>A (p.Cys992Tyr) rs2101548857
NM_000110.4(DPYD):c.299_302del (p.Phe100fs) rs72549309
NM_000110.4(DPYD):c.851-255A>G rs3790386
NM_000110.4(DPYD):c.958+135dup rs1397160848
NM_000110.4(DPYD):c.976T>C (p.Ser326Pro)

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