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. 2008 Oct 22;25(11-12):553–557. doi: 10.1007/s10815-008-9270-x

Table 2.

Genotype and allele frequencies of coding-nucleotide-polymorphism (cSNP) in human CDK2 in patient and control groups

Sequence change Classification of change Alteration in amino acid sequence Frequency of SNP in patients Frequency of SNP in controls Fisher’s exact test
Allele (%) Genotype (%) Allele (%) Genotype (%) AlleleP GenotypeP
Exon7 C(1038)G SNP1 Missense Thr→Ser 1/35 (2.8%) C/G 1/18(5.5%) 1/199 (0.50%) C/G 1/99 (1.01%) 0.282 0.282