ClinVar Miner

List of variants in gene DPYD reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP gnomAD frequency
NM_000110.4(DPYD):c.1371C>T (p.Asn457=) rs57918000 0.00785
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.1701A>T (p.Gly567=) rs148372305 0.00058
NM_000110.4(DPYD):c.1905C>T (p.Asn635=) rs3918289 0.00021
NM_000110.4(DPYD):c.2049C>G (p.Ala683=) rs183475941 0.00019
NM_000110.4(DPYD):c.1129A>G (p.Met377Val) rs144935781 0.00014
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.1990G>T (p.Ala664Ser) rs138545885 0.00006
NM_000110.4(DPYD):c.2071G>T (p.Val691Leu) rs202212118 0.00006
NM_000110.4(DPYD):c.1543G>A (p.Val515Ile) rs148994843 0.00005
NM_000110.4(DPYD):c.187A>G (p.Lys63Glu) rs367619008 0.00004
NM_000110.4(DPYD):c.474T>C (p.Phe158=) rs190771411 0.00004
NM_000110.4(DPYD):c.1048T>C (p.Ser350Pro) rs771885007 0.00001
NM_000110.4(DPYD):c.1337A>C (p.Lys446Thr) rs200709381 0.00001
NM_000110.4(DPYD):c.1415G>A (p.Ser472Asn) rs776082092 0.00001
NM_000110.4(DPYD):c.1538C>T (p.Ala513Val) rs760663364 0.00001
NM_000110.4(DPYD):c.632A>G (p.Tyr211Cys) rs72549307 0.00001
NM_000110.4(DPYD):c.1140T>C (p.Ala380=)
NM_000110.4(DPYD):c.1167A>G (p.Pro389=)
NM_000110.4(DPYD):c.1273C>G (p.Gln425Glu)
NM_000110.4(DPYD):c.1278G>T (p.Met426Ile)
NM_000110.4(DPYD):c.1293C>T (p.Ala431=)
NM_000110.4(DPYD):c.1311C>T (p.Ala437=)
NM_000110.4(DPYD):c.137A>C (p.Asp46Ala)
NM_000110.4(DPYD):c.1383C>T (p.Leu461=)
NM_000110.4(DPYD):c.1390G>A (p.Val464Ile)
NM_000110.4(DPYD):c.1444G>A (p.Val482Ile)
NM_000110.4(DPYD):c.1519G>A (p.Val507Ile)
NM_000110.4(DPYD):c.1524G>A (p.Gln508=)
NM_000110.4(DPYD):c.1554G>A (p.Lys518=)
NM_000110.4(DPYD):c.1602T>C (p.Ser534=)
NM_000110.4(DPYD):c.1650C>T (p.Ser550=)
NM_000110.4(DPYD):c.1670C>T (p.Thr557Ile)
NM_000110.4(DPYD):c.1671A>G (p.Thr557=)
NM_000110.4(DPYD):c.1683A>C (p.Arg561=)
NM_000110.4(DPYD):c.1728C>G (p.Phe576Leu)
NM_000110.4(DPYD):c.1729T>G (p.Ser577Ala)
NM_000110.4(DPYD):c.1744A>G (p.Ile582Val)
NM_000110.4(DPYD):c.1820T>C (p.Phe607Ser)
NM_000110.4(DPYD):c.185T>A (p.Ile62Asn)
NM_000110.4(DPYD):c.188A>C (p.Lys63Thr)
NM_000110.4(DPYD):c.189G>C (p.Lys63Asn)
NM_000110.4(DPYD):c.1906A>C (p.Ile636Leu)
NM_000110.4(DPYD):c.1907T>C (p.Ile636Thr)
NM_000110.4(DPYD):c.1937A>G (p.Asn646Ser)
NM_000110.4(DPYD):c.194C>T (p.Thr65Met)
NM_000110.4(DPYD):c.1984G>A (p.Ala662Thr)
NM_000110.4(DPYD):c.2047G>A (p.Ala683Thr)
NM_000110.4(DPYD):c.2075G>A (p.Arg692Gln)
NM_000110.4(DPYD):c.2075G>T (p.Arg692Leu)
NM_000110.4(DPYD):c.209G>A (p.Arg70Gln)
NM_000110.4(DPYD):c.2115T>A (p.Pro705=)
NM_000110.4(DPYD):c.2148T>A (p.Asp716Glu)
NM_000110.4(DPYD):c.218T>G (p.Leu73Arg)
NM_000110.4(DPYD):c.2269G>C (p.Ala757Pro)
NM_000110.4(DPYD):c.2283A>C (p.Thr761=)
NM_000110.4(DPYD):c.2320G>A (p.Ala774Thr)
NM_000110.4(DPYD):c.2335A>G (p.Thr779Ala)
NM_000110.4(DPYD):c.2567C>T (p.Thr856Ile)
NM_000110.4(DPYD):c.2593G>T (p.Val865Phe)
NM_000110.4(DPYD):c.261T>C (p.Cys87=)
NM_000110.4(DPYD):c.2654A>G (p.Gln885Arg)
NM_000110.4(DPYD):c.2705T>C (p.Val902Ala)
NM_000110.4(DPYD):c.2840T>C (p.Met947Thr)
NM_000110.4(DPYD):c.2848G>A (p.Glu950Lys)
NM_000110.4(DPYD):c.2864A>G (p.Asn955Ser)
NM_000110.4(DPYD):c.2948C>T (p.Thr983Ile)
NM_000110.4(DPYD):c.2950G>A (p.Asp984Asn)
NM_000110.4(DPYD):c.2992A>G (p.Ile998Val)
NM_000110.4(DPYD):c.3049G>A (p.Val1017Ile)
NM_000110.4(DPYD):c.3052C>G (p.Pro1018Ala)
NM_000110.4(DPYD):c.3067C>T (p.Pro1023Ser) rs114096998
NM_000110.4(DPYD):c.336T>G (p.Ala112=)
NM_000110.4(DPYD):c.340A>G (p.Lys114Glu)
NM_000110.4(DPYD):c.342G>A (p.Lys114=)
NM_000110.4(DPYD):c.367G>A (p.Gly123Ser)
NM_000110.4(DPYD):c.483+609T>C
NM_000110.4(DPYD):c.484-4G>A
NM_000110.4(DPYD):c.497T>C (p.Met166Thr)
NM_000110.4(DPYD):c.570T>C (p.Ile190=)
NM_000110.4(DPYD):c.591T>A (p.Pro197=)
NM_000110.4(DPYD):c.591T>C (p.Pro197=)
NM_000110.4(DPYD):c.623G>T (p.Arg208Leu) rs376073289
NM_000110.4(DPYD):c.73C>T (p.His25Tyr)
NM_000110.4(DPYD):c.768T>G (p.Ile256Met)
NM_000110.4(DPYD):c.770G>A (p.Cys257Tyr)
NM_000110.4(DPYD):c.841A>G (p.Ile281Val)
NM_000110.4(DPYD):c.877A>G (p.Ile293Val)
NM_000110.4(DPYD):c.879C>T (p.Ile293=)

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