ClinVar Miner

List of variants in gene DPYD reported as likely benign

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Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_000110.4(DPYD):c.1627A>G (p.Ile543Val) rs1801159 0.18679
NM_000110.4(DPYD):c.496A>G (p.Met166Val) rs2297595 0.08071
NM_000110.4(DPYD):c.2194G>A (p.Val732Ile) rs1801160 0.03794
NM_000110.4(DPYD):c.*900T>C rs17470762 0.02724
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.483+279C>A rs79063448 0.01213
NM_000110.4(DPYD):c.1371C>T (p.Asn457=) rs57918000 0.00785
NM_000110.4(DPYD):c.2058+157G>A rs115139529 0.00747
NM_000110.4(DPYD):c.151-69G>A rs115632870 0.00703
NM_000110.4(DPYD):c.557A>G (p.Tyr186Cys) rs115232898 0.00622
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.484-145T>A rs78682297 0.00477
NM_000110.4(DPYD):c.2908-208A>G rs76665493 0.00437
NM_000110.4(DPYD):c.1128+161G>A rs74105265 0.00414
NM_000110.4(DPYD):c.2846A>T (p.Asp949Val) rs67376798 0.00334
NM_000110.4(DPYD):c.1525-11G>A rs55699321 0.00166
NM_000110.4(DPYD):c.2180-3T>C rs74104343 0.00158
NM_000110.4(DPYD):c.1701A>T (p.Gly567=) rs148372305 0.00058
NM_000110.4(DPYD):c.2766+19A>G rs375268978 0.00056
NM_000110.4(DPYD):c.2915A>G (p.Gln972Arg) rs145529148 0.00054
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.1905C>T (p.Asn635=) rs3918289 0.00021
NM_000110.4(DPYD):c.525G>A (p.Ser175=) rs6670886 0.00019
NM_000110.4(DPYD):c.2303C>A (p.Thr768Lys) rs56005131 0.00011
NM_000110.4(DPYD):c.258G>A (p.Pro86=) rs201841475 0.00009
NM_000110.4(DPYD):c.2049C>G (p.Ala683=) rs183475941 0.00008
NM_000110.4(DPYD):c.1280T>C (p.Val427Ala) rs200693895 0.00005
NM_000110.4(DPYD):c.474T>C (p.Phe158=) rs190771411 0.00004
NM_000110.4(DPYD):c.1796T>C (p.Met599Thr) rs147601618 0.00003
NM_000110.4(DPYD):c.2179+4A>G rs746718279 0.00001
NM_000110.4(DPYD):c.2279C>T (p.Thr760Ile) rs112766203 0.00001
NM_000110.4(DPYD):c.2299+7G>A rs369672458 0.00001
NM_000110.4(DPYD):c.1020T>G (p.Ala340=)
NM_000110.4(DPYD):c.1140T>C (p.Ala380=)
NM_000110.4(DPYD):c.1167A>G (p.Pro389=)
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.1349C>T (p.Ala450Val) rs72975710
NM_000110.4(DPYD):c.1383C>T (p.Leu461=)
NM_000110.4(DPYD):c.1444G>A (p.Val482Ile)
NM_000110.4(DPYD):c.1519G>A (p.Val507Ile)
NM_000110.4(DPYD):c.1554G>A (p.Lys518=)
NM_000110.4(DPYD):c.1602T>C (p.Ser534=)
NM_000110.4(DPYD):c.1617A>G (p.Gly539=)
NM_000110.4(DPYD):c.1650C>T (p.Ser550=)
NM_000110.4(DPYD):c.1671A>G (p.Thr557=)
NM_000110.4(DPYD):c.1683A>C (p.Arg561=)
NM_000110.4(DPYD):c.2115T>A (p.Pro705=)
NM_000110.4(DPYD):c.2223G>C (p.Leu741=)
NM_000110.4(DPYD):c.2283A>C (p.Thr761=)
NM_000110.4(DPYD):c.2421T>C (p.His807=)
NM_000110.4(DPYD):c.2442+69dup rs544905665
NM_000110.4(DPYD):c.2550T>C (p.Asp850=)
NM_000110.4(DPYD):c.2586G>A (p.Gly862=)
NM_000110.4(DPYD):c.261T>C (p.Cys87=)
NM_000110.4(DPYD):c.2623-8C>T rs1570451084
NM_000110.4(DPYD):c.2646T>C (p.Tyr882=)
NM_000110.4(DPYD):c.2705T>C (p.Val902Ala)
NM_000110.4(DPYD):c.279T>C (p.Thr93=) rs2101070143
NM_000110.4(DPYD):c.2976T>C (p.Cys992=)
NM_000110.4(DPYD):c.2994T>C (p.Ile998=)
NM_000110.4(DPYD):c.3062T>C (p.Val1021Ala)
NM_000110.4(DPYD):c.3067C>A (p.Pro1023Thr) rs114096998
NM_000110.4(DPYD):c.336T>G (p.Ala112=)
NM_000110.4(DPYD):c.342G>A (p.Lys114=)
NM_000110.4(DPYD):c.45C>A (p.Ile15=) rs267598790
NM_000110.4(DPYD):c.483+604T>A
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.771C>T (p.Cys257=)
NM_000110.4(DPYD):c.879C>T (p.Ile293=)
NM_000110.4(DPYD):c.958+135dup rs1397160848
NM_000110.4(DPYD):c.966C>T (p.Cys322=)

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