List of variants in gene CPT1A reported as likely benign for not specified

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001876.4(CPT1A):c.823G>A (p.Ala275Thr)	rs2229738	0.05682
NM_001876.4(CPT1A):c.2142G>A (p.Pro714=)	rs150792109	0.00081
NM_001876.4(CPT1A):c.453+9G>A	rs183694834	0.00070
NM_001876.4(CPT1A):c.2142+8C>T	rs147563740	0.00054
NM_001876.4(CPT1A):c.144C>T (p.Asn48=)	rs182451427	0.00043
NM_001876.4(CPT1A):c.1983C>T (p.Tyr661=)	rs374136875	0.00036
NM_001876.4(CPT1A):c.142-16G>A	rs201717907	0.00027
NM_001876.4(CPT1A):c.1770G>A (p.Glu590=)	rs61731905	0.00016
NM_001876.4(CPT1A):c.357C>T (p.Ile119=)	rs138011726	0.00015
NM_001876.4(CPT1A):c.192C>T (p.Ile64=)	rs142691028	0.00010
NM_001876.4(CPT1A):c.2142+9G>A	rs753764564	0.00005
NM_001876.4(CPT1A):c.1353-4G>A	rs577271875	0.00004
NM_001876.4(CPT1A):c.1461C>T (p.Tyr487=)	rs757568196	0.00003
NM_001876.4(CPT1A):c.2235+4T>C	rs755308448	0.00003
NM_001876.4(CPT1A):c.556-7A>T	rs1057523637	0.00003
NM_001876.4(CPT1A):c.1575+8C>T	rs372364901	0.00002
NM_001876.4(CPT1A):c.693C>T (p.Tyr231=)	rs146551320	0.00001
NM_001876.4(CPT1A):c.694-9G>A	rs771162679	0.00001
NM_001876.4(CPT1A):c.-49TGCCGC[1]	rs528519032
NM_001876.4(CPT1A):c.-49TGCCGC[2]	rs528519032
NM_001876.4(CPT1A):c.-49TGCCGC[4]	rs528519032
NM_001876.4(CPT1A):c.-49TGCCGC[5]	rs528519032
NM_001876.4(CPT1A):c.1740+15C>T	rs1363762969
NM_001876.4(CPT1A):c.1875+6G>A	rs1555226547
NM_001876.4(CPT1A):c.282-14G>A	rs1555231768
NM_001876.4(CPT1A):c.771+13G>A	rs996371611
NM_001876.4(CPT1A):c.771+17G>C	rs201034164

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