Table 2.

Genotyped KIR alleles in CML patients; duplicated allele were not observed

NumberFrequency
KIR2DL2/3
 3*00113689.5%
 2*003117.2%
 3*02321.3%
 2*00110.7%
 3*00910.7%
 3*01910.7%
KIR2DL1
 *00312884.2%
 *002127.9%
 *00410.7%
 Blank117.2%
KIR2DL4
 *0017650.0%
 *005/0114227.6%
 *0062415.8%
 *00895.9%
 Blank10.7%
KIR3DL1/S1
 *0156945.4%
 *0072415.8%
 3DS1*0132315.1%
 *005159.9%
 *00195.9%
 *02053.3%
 3DS1*08532.0%
 *02910.7%
 *03810.7%
 3DS1*07810.7%
 Blank10.7%
KIR2DS1
 *0022617.1%
 *002/00321.3%
 Blank12481.6%
KIR2DS4
 *0016945.4%
 *004159.9%
 *004-variant95.9%
 *003149.2%
 *007/01095.9%
 *014/01663.9%
 *01521.3%
 Blank2818.4%
KIR3DL2
 *0027046.1%
 *0072315.1%
 *0082013.2%
 *0101811.8%
 *00995.9%
 *001/*04932.0%
 *01532.0%
 *01621.3%
 *02121.3%
 *02410.7%
 *02710.7%
  • NOTE: As KIR2DL2/DL3 and KIR3DL1/DS1 alleles are shared within the same gene, they are shown in the same category KIR2DL2/3 and KIR3DL1/S1, respectively. KIR2DS4*004 variant is the allele that changed aspartic acid (D) to valine (V) at codon 57 in *004.