Abstract

We built a molecular typing protocol of the ss469415590 SNP in the IFNL4 gene based on the real-time PCR technique with two Taqman probes which are specific for each allele of ss469415590. The protocol includes: (1) DNA extraction from whole blood; (2) DNA amplification in real-time PCR reactions with the primer pair of ss469415590_IFNL4_F - ss469415590_IFNL4_R and two speific Taqman probes ss469415590_IFNL4_FAM for the G allele and ss469415590_IFNL4_VIC for the TT allele. The typing protocol was evaluated on 95 clinical DNA samples. The allele frequencies were calculated as 93 % for the TT allele and 7 % for the G allele. The comparison of the typing protocol to the sequencing method revealed 100 % identical results.