List of variants in gene CPT2 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000098.3(CPT2):c.1634A>C (p.Glu545Ala)	rs17848485	0.00067
NM_000098.3(CPT2):c.1602G>A (p.Glu534=)	rs148110518	0.00037
NM_000098.3(CPT2):c.1048C>T (p.Arg350Cys)	rs151003641	0.00025
NM_000098.3(CPT2):c.365C>T (p.Ser122Phe)	rs192275019	0.00014
NM_000098.3(CPT2):c.921G>A (p.Met307Ile)	rs745698305	0.00005
NM_000098.3(CPT2):c.665A>G (p.Asn222Ser)	rs760978599	0.00001
NM_000098.3(CPT2):c.1430G>A (p.Arg477Gln)
NM_000098.3(CPT2):c.1769G>A (p.Ser590Asn)
NM_000098.3(CPT2):c.1954G>A (p.Glu652Lys)	rs766154734
NM_000098.3(CPT2):c.701T>C (p.Leu234Pro)

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