List of variants reported as likely benign for Carnitine palmitoyl transferase II deficiency, severe infantile form; Carnitine palmitoyl transferase II deficiency, myopathic form; Carnitine palmitoyl transferase II deficiency, neonatal form; Encephalopathy, acute, infection-induced, susceptibility to, 4

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000098.3(CPT2):c.1767G>A (p.Thr589=)	rs77565483	0.01032
NM_000098.3(CPT2):c.1578T>C (p.Gly526=)	rs113493395	0.00455
NM_000098.3(CPT2):c.1776G>A (p.Leu592=)	rs141146189	0.00023
NM_000098.3(CPT2):c.399A>G (p.Pro133=)	rs375573986	0.00019
NM_000098.3(CPT2):c.103C>T (p.Leu35=)	rs2929073	0.00003
NM_000098.3(CPT2):c.1290T>C (p.Ala430=)	rs776488578	0.00001
NM_000098.3(CPT2):c.135C>T (p.Tyr45=)	rs1645327989	0.00001
NM_000098.3(CPT2):c.1851T>C (p.His617=)	rs540322467	0.00001
NM_000098.3(CPT2):c.222T>C (p.Asp74=)	rs1360477206	0.00001
NM_000098.3(CPT2):c.378C>T (p.Ser126=)	rs780743357	0.00001
NM_000098.3(CPT2):c.468T>C (p.Thr156=)	rs138938770	0.00001
NM_000098.3(CPT2):c.1080C>T (p.Ile360=)	rs749833236
NM_000098.3(CPT2):c.1509C>T (p.Arg503=)	rs1572385867
NM_000098.3(CPT2):c.15G>C (p.Leu5=)	rs1443908294
NM_000098.3(CPT2):c.1645+14G>T	rs2100274977

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