List of variants reported as benign for Dihydropyrimidinase deficiency by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001385.3(DPYS):c.-1T>C	rs2959023	0.61425
NM_001385.3(DPYS):c.216C>T (p.Phe72=)	rs2298840	0.20920
NM_001385.3(DPYS):c.15G>A (p.Ser5=)	rs182332679	0.03516
NM_001385.3(DPYS):c.672A>G (p.Ala224=)	rs7825427	0.02132
NM_001385.3(DPYS):c.541C>T (p.Arg181Trp)	rs36027551	0.01325
NM_001385.3(DPYS):c.1350C>T (p.Ala450=)	rs75490773	0.00805
NM_001385.3(DPYS):c.1029C>G (p.Thr343=)	rs117104587	0.00736
NM_001385.3(DPYS):c.*148C>T	rs142452664	0.00494
NM_001385.3(DPYS):c.1092+9C>T	rs138453168	0.00444
NM_001385.3(DPYS):c.765T>C (p.Ala255=)	rs35371065	0.00426
NM_001385.3(DPYS):c.17G>A (p.Arg6Gln)	rs199618701	0.00034
NM_001385.3(DPYS):c.*65T>C	rs151260693	0.00019
NM_001385.3(DPYS):c.*344T>A	rs73699419

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