Table 2.
Localization | DNA Alteration | Cases (n) | Allele Frequency of MPNST Patients | Allele Frequency of Controls | |
Intron 2 | Nucleic acid 11827 | G→C | 13 (heterozygous), 1 (homozygous) | 0.21 (C11827) | 0.31 (C11827) |
Intron 3 | Nucleic acid 11951 | Duplication, GGGGACCTGGAGGCT | 11 (heterozygous) | 0.15 (16-bp dup) | 0.16 (16-bp dup) |
Intron 3 | Nucleic acid 11992 | C→A | 3 (heterozygous) | 0.032 (A11992) | 0.041 (A11992) |
Exon 4 | Codon 72 | CGC→CCC | 15 (heterozygous) | 0.21 (p53Pro72) | 0.26 (p53Pro72) |
The position of polymorphisms is given according to reference X54156 (NCBI database).