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. 2007 Aug;9(8):671–677. doi: 10.1593/neo.07304

Table 2.

TP53 Polymorphisms in MPNST Patients.

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).