Mitochondrial carnitine palmitoyltransferase-II dysfunction: A possible novel mechanism for nonalcoholic fatty liver disease in hepatocarcinogenesis

Table 1 Summary of CPT2 gene and reported mutation sites

Exon	Size in bp	Nucleotides	Amino acids	Mut. no.	Mutation sites
					Amino acids	Others
1	668	1-668	1-51	5	2	3
2	81	669-749	52-78	4	2	2
3	107	750-856	79-113	5	3	2
4	1305	857-2161	114-548	59	49	10
5	929	2162-3090	549-658	16	12	4

Mut no.: Total numbers of nucleotide mutation including insertion, delete or peptide variation from codon substitution; Others: Mutations from double or more nucleotide insertion, deletes and so on.