List of variants reported as uncertain significance for 3-methylcrotonyl-CoA carboxylase deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_022132.5(MCCC2):c.1322T>C (p.Ile441Thr)	rs139852818	0.00137
NM_022132.5(MCCC2):c.1433C>G (p.Ala478Gly)	rs35068278	0.00082
NM_020166.5(MCCC1):c.1792C>A (p.Leu598Met)	rs138480247	0.00075
NM_020166.5(MCCC1):c.1942G>A (p.Gly648Ser)	rs149017703	0.00056
NM_020166.5(MCCC1):c.1894C>T (p.Pro632Ser)	rs142867987	0.00015
NM_022132.5(MCCC2):c.746C>T (p.Ala249Val)	rs141676987	0.00015
NM_020166.5(MCCC1):c.1561G>A (p.Ala521Thr)	rs149957640	0.00012
NM_020166.5(MCCC1):c.1715G>C (p.Gly572Ala)	rs182830931	0.00003
NM_020166.5(MCCC1):c.2089G>A (p.Val697Met)	rs776138490	0.00003
NM_022132.5(MCCC2):c.1206A>G (p.Gln402=)	rs749406136	0.00003
NM_020166.5(MCCC1):c.1261C>T (p.Arg421Trp)	rs764744442	0.00001
NM_020166.5(MCCC1):c.1703A>G (p.Tyr568Cys)	rs1577245387	0.00001
NM_020166.5(MCCC1):c.793C>T (p.His265Tyr)	rs767642062	0.00001
NM_022132.5(MCCC2):c.1635dup (p.Ser546Ter)	rs768272570
NM_022132.5(MCCC2):c.433T>C (p.Tyr145His)	rs1745481314

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