ClinVar Miner

List of variants in gene DPYD reported as uncertain significance by Counsyl

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000110.4(DPYD):c.2872A>G (p.Lys958Glu) rs141044036 0.00006
NM_000110.4(DPYD):c.1475C>T (p.Ser492Leu) rs72549304 0.00004
NM_000110.4(DPYD):c.1651G>A (p.Ala551Thr) rs777425216 0.00004
NM_000110.4(DPYD):c.187A>G (p.Lys63Glu) rs367619008 0.00004
NM_000110.4(DPYD):c.1555C>T (p.Pro519Ser) rs672601282 0.00003
NM_000110.4(DPYD):c.1775G>A (p.Arg592Gln) rs138616379 0.00003
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.1024G>A (p.Asp342Asn) rs183385770 0.00001
NM_000110.4(DPYD):c.1538C>T (p.Ala513Val) rs760663364 0.00001
NM_000110.4(DPYD):c.2276G>A (p.Arg759Gln) rs267598786 0.00001
NM_000110.4(DPYD):c.632A>G (p.Tyr211Cys) rs72549307 0.00001
NM_000110.4(DPYD):c.704G>A (p.Arg235Gln) rs755416212 0.00001
NM_000110.4(DPYD):c.1070G>A (p.Arg357His) rs377143350
NM_000110.4(DPYD):c.2168C>G (p.Ala723Gly) rs1553251908
NM_000110.4(DPYD):c.2822T>C (p.Val941Ala) rs748639205
NM_000110.4(DPYD):c.2908-1G>A rs1553209268
NM_000110.4(DPYD):c.3031dup (p.Tyr1011fs) rs1459699844

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