List of variants in gene CPT1C reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001199753.2(CPT1C):c.2092A>G (p.Asn698Asp)	rs143091111	0.00049
NM_001199753.2(CPT1C):c.1286C>T (p.Pro429Leu)	rs368513098	0.00003
NM_001199753.2(CPT1C):c.1220C>A (p.Ala407Glu)
NM_001199753.2(CPT1C):c.1763C>T (p.Ser588Leu)
NM_001199753.2(CPT1C):c.1874A>G (p.Gln625Arg)

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