| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Duplication (inframe_insertion +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Duplication (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency +2 more | |
| | | Single nucleotide variant (intron variant) | Carnitine palmitoyl transferase 1A deficiency +1 more | |
| | | Single nucleotide variant (splice donor variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Deletion (frameshift variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Deletion | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (missense variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (nonsense) | Carnitine palmitoyl transferase 1A deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Carnitine palmitoyl transferase 1A deficiency | |
| | | Single nucleotide variant (nonsense) | Carnitine palmitoyl transferase 1A deficiency | |