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The novel HLA-C*03:621 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individual
Fu-Ming Zi1, Zhong-Zheng Zheng2, Ke-Ming Du2
1Department of Hematology, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
HLA
|March 8, 2023
Abstract:
HLA-C*03:621 differs from HLA-C*03:04:01:01 by one nucleotide in exon 1.
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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...

