Variants in gene CPT2 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

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HGVS	dbSNP	gnomAD frequency
NM_000098.3(CPT2):c.338C>T (p.Ser113Leu)	rs74315294	0.00134
NM_000098.3(CPT2):c.359A>G (p.Tyr120Cys)	rs121918528	0.00006
NM_000098.3(CPT2):c.1511C>T (p.Pro504Leu)	rs368311455	0.00003
NM_000098.3(CPT2):c.1148T>A (p.Phe383Tyr)	rs74315295	0.00001
NM_000098.3(CPT2):c.1507C>T (p.Arg503Cys)	rs74315296	0.00001
NM_000098.3(CPT2):c.341-2A>G	rs752468216	0.00001
NM_000098.3(CPT2):c.370C>T (p.Arg124Ter)	rs201065226	0.00001
NM_000098.3(CPT2):c.452G>A (p.Arg151Gln)	rs515726177	0.00001
NM_000098.3(CPT2):c.481C>T (p.Arg161Trp)	rs756839691	0.00001
NM_000098.3(CPT2):c.520G>A (p.Glu174Lys)	rs28936674	0.00001
NM_000098.3(CPT2):c.1324dup (p.Thr442fs)	rs1131691330
NM_000098.3(CPT2):c.1569_1570del (p.His523fs)	rs1572385947
NM_000098.3(CPT2):c.1784del (p.Pro595fs)	rs760255368
NM_000098.3(CPT2):c.1816_1817del (p.Val606fs)	rs908749525
NM_000098.3(CPT2):c.1883A>C (p.Tyr628Ser)	rs28936673
NM_000098.3(CPT2):c.852del (p.Glu285fs)	rs1057517729

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