List of variants reported as benign for Deficiency of acetyl-CoA acetyltransferase by Illumina Laboratory Services, Illumina

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000019.3(ACAT1):c.*599A>C	rs2280332	0.28837
NM_000019.4(ACAT1):c.13G>C (p.Ala5Pro)	rs3741056	0.27945
NM_000019.4(ACAT1):c.-9T>A	rs3741055	0.26111
NM_000019.4(ACAT1):c.471C>A (p.Ser157=)	rs35188041	0.16806
NM_000019.4(ACAT1):c.-15C>G	rs113348145	0.02192
NM_000019.3(ACAT1):c.*555A>G	rs111376037	0.01843
NM_000019.4(ACAT1):c.*179T>G	rs114728153	0.01290
NM_000019.3(ACAT1):c.*250C>T	rs79179095	0.01146
NM_000019.3(ACAT1):c.*293A>T	rs73559273	0.00975
NM_000019.3(ACAT1):c.*507G>A	rs12271846	0.00968
NM_000019.4(ACAT1):c.978A>C (p.Pro326=)	rs73559264	0.00941
NM_000019.3(ACAT1):c.*214G>C	rs145690535	0.00839
NM_000019.4(ACAT1):c.903G>A (p.Ala301=)	rs75811190	0.00390
NM_000019.4(ACAT1):c.1068T>C (p.Phe356=)	rs139657823	0.00308
NM_000019.4(ACAT1):c.-28T>A	rs36216231	0.00247
NM_000019.3(ACAT1):c.777_780delAATT	rs112801981
NM_000019.4(ACAT1):c.-22C>G	rs3741054
NM_000019.4(ACAT1):c.436-4G>A	rs3741050

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