List of variants in gene CPT2 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000098.3(CPT2):c.1102G>A (p.Val368Ile)	rs1799821	0.46024
NM_000098.3(CPT2):c.1939A>G (p.Met647Val)	rs1799822	0.15237
NM_000098.3(CPT2):c.511C>T (p.Leu171=)	rs2229292	0.02118
NM_000098.3(CPT2):c.1055T>G (p.Phe352Cys)	rs2229291	0.01469
NM_000098.3(CPT2):c.1767G>A (p.Thr589=)	rs77565483	0.01032
NM_000098.3(CPT2):c.302C>T (p.Ala101Val)	rs75939866	0.00675
NM_000098.3(CPT2):c.1578T>C (p.Gly526=)	rs113493395	0.00455
NM_000098.3(CPT2):c.1763C>G (p.Ser588Cys)	rs1871748	0.00353
NM_000098.3(CPT2):c.338C>T (p.Ser113Leu)	rs74315294	0.00134
NM_000098.3(CPT2):c.1025T>C (p.Met342Thr)	rs144658100	0.00110
NM_000098.3(CPT2):c.353A>G (p.Asp118Gly)	rs148035648	0.00085
NM_000098.3(CPT2):c.1598T>C (p.Val533Ala)	rs144703247	0.00048
NM_000098.3(CPT2):c.680C>T (p.Pro227Leu)	rs74315298	0.00039
NM_000098.3(CPT2):c.1602G>A (p.Glu534=)	rs148110518	0.00037
NM_000098.3(CPT2):c.1049G>A (p.Arg350His)	rs773966429	0.00001

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