ClinVar Miner

List of variants in gene DPYD studied for not specified

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_000110.4(DPYD):c.85T>C (p.Cys29Arg) rs1801265 0.27966
NM_000110.4(DPYD):c.1627A>G (p.Ile543Val) rs1801159 0.18679
NM_000110.4(DPYD):c.1129-15T>C rs56293913 0.09765
NM_000110.4(DPYD):c.496A>G (p.Met166Val) rs2297595 0.08071
NM_000110.4(DPYD):c.1896T>C (p.Phe632=) rs17376848 0.04278
NM_000110.4(DPYD):c.2194G>A (p.Val732Ile) rs1801160 0.03794
NM_000110.4(DPYD):c.1218G>A (p.Met406Ile) rs61622928 0.02183
NM_000110.4(DPYD):c.1601G>A (p.Ser534Asn) rs1801158 0.01380
NM_000110.4(DPYD):c.483+18G>A rs56276561 0.01302
NM_000110.4(DPYD):c.1236G>A (p.Glu412=) rs56038477 0.01297
NM_000110.4(DPYD):c.557A>G (p.Tyr186Cys) rs115232898 0.00622
NM_000110.4(DPYD):c.775A>G (p.Lys259Glu) rs45589337 0.00513
NM_000110.4(DPYD):c.2180-3T>C rs74104343 0.00158
NM_000110.4(DPYD):c.2485G>A (p.Asp829Asn) rs199777072 0.00130
NM_000110.4(DPYD):c.868A>G (p.Lys290Glu) rs146356975 0.00078
NM_000110.4(DPYD):c.451A>G (p.Asn151Asp) rs200562975 0.00049
NM_000110.4(DPYD):c.1524+16C>A rs199469537 0.00048
NM_000110.4(DPYD):c.1615G>A (p.Gly539Arg) rs142619737 0.00032
NM_000110.4(DPYD):c.2180-11G>A rs377136032 0.00032
NM_000110.4(DPYD):c.1358C>G (p.Pro453Arg) rs144395748 0.00031
NM_000110.4(DPYD):c.1774C>T (p.Arg592Trp) rs59086055 0.00006
NM_000110.4(DPYD):c.1280T>C (p.Val427Ala) rs200693895 0.00005
NM_000110.4(DPYD):c.321+15A>C rs370363977 0.00004
NM_000110.4(DPYD):c.1796T>C (p.Met599Thr) rs147601618 0.00003
NM_000110.4(DPYD):c.2378C>T (p.Thr793Ile) rs547099198 0.00003
NM_000110.4(DPYD):c.2657G>A (p.Arg886His) rs1801267 0.00003
NM_000110.4(DPYD):c.1108A>G (p.Ile370Val) rs72549305 0.00002
NM_000110.4(DPYD):c.545T>A (p.Met182Lys) rs779728902 0.00002
NM_000110.4(DPYD):c.3034G>T (p.Glu1012Ter) rs761584058 0.00001
NM_000110.4(DPYD):c.632A>G (p.Tyr211Cys) rs72549307 0.00001
GRCh37/hg19 1p21.3(chr1:97545589-97594994)
GRCh37/hg19 1p21.3(chr1:97697334-98471128)
NC_000001.10:g.(97548027_97564044)_(97564189_97658624)del
NC_000001.10:g.(97848018_97915614)_(97981498_98015115)dup
NM_000110.4(DPYD):c.1537G>C (p.Ala513Pro)
NM_000110.4(DPYD):c.2907+9C>G
NM_000110.4(DPYD):c.2976T>C (p.Cys992=)
NM_000110.4(DPYD):c.3040_3041del (p.Lys1014fs)
NM_000110.4(DPYD):c.3067C>A (p.Pro1023Thr) rs114096998
NM_000110.4(DPYD):c.3067C>T (p.Pro1023Ser) rs114096998
NM_000110.4(DPYD):c.623G>A (p.Arg208Gln)
NM_000110.4(DPYD):c.710C>T (p.Pro237Leu)
NM_000110.4(DPYD):c.731A>C (p.Glu244Ala)
NM_000110.4(DPYD):c.967G>A (p.Ala323Thr)

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