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

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_022132.5(MCCC2):c.599T>A (p.Ile200Asn)	rs140806722	0.00262
NM_020166.5(MCCC1):c.1942G>A (p.Gly648Ser)	rs149017703	0.00056
NM_020166.5(MCCC1):c.1561G>A (p.Ala521Thr)	rs149957640	0.00012
NM_020166.5(MCCC1):c.898A>G (p.Lys300Glu)	rs753650692	0.00002
NM_020166.5(MCCC1):c.635G>C (p.Gly212Ala)	rs749287771	0.00001
NM_020166.5(MCCC1):c.130_131delinsTT (p.Ala44Phe)	rs1553868919
NM_020166.5(MCCC1):c.1782C>G (p.Asp594Glu)
NM_020166.5(MCCC1):c.310C>A (p.Gln104Lys)	rs1177891822
NM_020166.5(MCCC1):c.386G>A (p.Cys129Tyr)
NM_022132.5(MCCC2):c.1493C>T (p.Ser498Phe)
NM_022132.5(MCCC2):c.1501G>A (p.Asp501Asn)	rs1391085331
NM_022132.5(MCCC2):c.955G>A (p.Gly319Arg)	rs1443551700

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