List of variants reported as uncertain significance for 3-methylcrotonyl-CoA carboxylase 2 deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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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_022132.5(MCCC2):c.746C>T (p.Ala249Val)	rs141676987	0.00015
NM_022132.5(MCCC2):c.1206A>G (p.Gln402=)	rs749406136	0.00003
NM_022132.5(MCCC2):c.1635dup (p.Ser546Ter)	rs768272570
NM_022132.5(MCCC2):c.433T>C (p.Tyr145His)	rs1745481314

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