List of variants in gene combination LOC129938008, MCCC1 reported as uncertain significance for 3-methylcrotonyl-CoA carboxylase deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_020166.5(MCCC1):c.-23C>T	rs374636986	0.00051
NM_020166.5(MCCC1):c.9G>A (p.Ala3=)	rs1191355416	0.00001
NM_020166.4(MCCC1):c.-101C>T	rs886058210
NM_020166.4(MCCC1):c.-102C>A	rs543130921
NM_020166.5(MCCC1):c.17C>T (p.Ala6Val)
NM_020166.5(MCCC1):c.5C>A (p.Ala2Glu)

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