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Updated: Jul 14, 2026

Wild-type Blocking PCR Combined with Sanger Sequencing for Detection of Low-frequency Somatic Mutation
Published on: August 23, 2024
Identification of a rare mutation in a TH01 primer binding site
Tomohiro Takayama1, Naoki Takada, Rie Suzuki
1Criminal Investigation Laboratory, Gifu Prefectural Police Headquarters, 2-1-1 Yabuta minami, Gifu City, Gifu 500-8501, Japan. tomohirot2001@yahoo.co.jp
Abstract:
We experienced a difficult case of TH01 typing. Instability of TH01 allele 9.3 was observed using GenePrint STR System TH01. Allele dropout was observed when an AmpFlSTR Profiler Kit was subsequently used for confirmation of the TH01 type. Use of the PowerPlex 16 System made it possible to detect allele 9.3. As a result of sequencing, a single point mutation (G-to-A transition) located 37 bases upstream of the first TCAT motif of the repeat region was identified as the cause of the allele dropout during use of the AmpFlSTR Profiler Kit. This mutation was located at the 3' end of the forward primers of the AmpFlSTR Profiler Kit and GenePrint STR System TH01.

