List of variants in gene CPT1A reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001876.4(CPT1A):c.145G>A (p.Gly49Ser)	rs552007692	0.00008
NM_001876.4(CPT1A):c.1784G>A (p.Arg595Gln)	rs763226691	0.00001
NM_001876.4(CPT1A):c.417G>C (p.Glu139Asp)	rs767840321	0.00001
NM_001876.4(CPT1A):c.1429G>A (p.Asp477Asn)
NM_001876.4(CPT1A):c.734G>A (p.Arg245Gln)

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