ClinVar Miner

List of variants in gene DPYD reported as uncertain significance for not specified

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_000110.4(DPYD):c.868A>G (p.Lys290Glu) rs146356975 0.00078
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.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.3040_3041del (p.Lys1014fs)
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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