An object of the present invention is to provide an allele specific primer which is accompanied by less possibility of the false positive and enables definite discrimination when a base immediately adjacent to on the 3' side of a target SNP base is C, while a base adjacent with one base spaced apart is T.According to the present invention, the 3' end base is designed to be the base corresponding to SNP; the second base from the 3' end to be T; the third base from the 3' end to be any one of T, G or C; and the base sequence of from the fourth from the 3' end to the 5' end base to be completely complementary to the sequence of from a base three bases away from the target SNP base on the 3' side to a desired base.

 
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> Methods for variation detection

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