ClinVar Miner

List of variants in gene DPYD reported as benign for not provided

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Gene type:
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Total variants: 62
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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.85= (p.Cys29=) rs1801265 0.72034
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.85T>C (p.Cys29Arg) rs1801265 0.27966
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.1627A>G (p.Ile543Val) rs1801159 0.18679
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.496A>G (p.Met166Val) rs2297595 0.08071
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.681-8C>T rs74774246 0.01331
NM_000110.4(DPYD):c.1236G>A (p.Glu412=) rs56038477 0.01297
NM_000110.4(DPYD):c.1129-5923C>G rs75017182 0.01296
NM_000110.4(DPYD):c.1371C>T (p.Asn457=) rs57918000 0.00785
NM_000110.4(DPYD):c.483+601C>G rs72977734 0.00584
NM_000110.4(DPYD):c.1494A>G (p.Gln498=) rs116364703 0.00519
NM_000110.4(DPYD):c.775A>G (p.Lys259Glu) rs45589337 0.00513
NM_000110.4(DPYD):c.2846A>T (p.Asp949Val) rs67376798 0.00334
NM_000110.4(DPYD):c.451A>G (p.Asn151Asp) rs200562975 0.00049
NM_000110.4(DPYD):c.1905C>T (p.Asn635=) rs3918289 0.00021
GRCh37/hg19 1p21.3(chr1:97457893-97721488)x3
GRCh37/hg19 1p21.3(chr1:97686885-98489080)x3
GRCh37/hg19 1p21.3(chr1:98059803-98079674)x3
GRCh37/hg19 1p21.3(chr1:98155074-98170206)x1
GRCh37/hg19 1p21.3(chr1:98191375-98327831)x1
GRCh37/hg19 1p21.3(chr1:98251973-98316285)x1
NC_000001.11:g.97921399A>C rs61787828
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.2058+145T>C rs1879374
NM_000110.4(DPYD):c.2442+283G>A rs11808108
NM_000110.4(DPYD):c.2907+55C>T rs290854
NM_000110.4(DPYD):c.3067C>A (p.Pro1023Thr) rs114096998
NM_000110.4(DPYD):c.851-255A>G rs3790386

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