Detection of the HLA‐A*02:759 allele, a variant of A*02:06:01:01, in a Taiwanese individual
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DOI: 10.1111/tan.14769
Abstract: A nucleotide mutation in exon 1 of HLA‐A*02:06:01:01 results in the novel allele, HLA‐A*02:759. read more here.
Keywords: hla 759; detection hla; variant taiwanese; taiwanese individual ... See more keywords
Recognition of the HLA‐A*02:07:19 allele, a variant of HLA‐A*02:07:01:01, in a Taiwanese individual
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DOI: 10.1111/tan.14772
Abstract: One nucleotide substitution at codon 310 of HLA‐A*02:07:01:01 results in the novel allele, HLA*02*07:19. read more here.
Keywords: hla; hla allele; recognition hla; variant hla ... See more keywords
Identification of HLA‐C*03:599 novel allele variant in two South Indian individuals in a Brahmin family
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DOI: 10.1111/tan.14815
Abstract: The novel allele HLA‐C*03:599 as compared with HLA‐C*03:04:01:02 displays polymorphism at position; gDNA 1618 (G>T). read more here.
Keywords: hla 599; 599 novel; variant two; novel allele ... See more keywords
Detection of the HLA‐B*40:02:03 allele, a variant of HLA‐B*40:02:01:01, in a Taiwanese individual
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DOI: 10.1111/tan.14972
Abstract: One nucleotide substitution in codon 67 of HLA‐B*40:02:01:01 results in a novel allele, HLA‐B*40:02:03. read more here.
Keywords: hla; detection hla; hla allele; variant hla ... See more keywords
Identification of a novel ABO*A1.02 allele with variant c.671T>C
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DOI: 10.1111/trf.17206
Abstract: As the first discovered blood group system, the ABO blood group plays a critical role in blood transfusion and hemolytic disease in newborns. Subgroup phenotypes, such as A2, Aint, A3, cisAB, B3, and Bel, have… read more here.
Keywords: novel abo; variant 671t; blood; abo allele ... See more keywords
Pharmacogenetic allele variant frequencies: An analysis of the VA’s Million Veteran Program (MVP) as a representation of the diversity in US population
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DOI: 10.1371/journal.pone.0274339
Abstract: We present allele frequencies of pharmacogenomics relevant variants across multiple ancestry in a sample representative of the US population. We analyzed 658,582 individuals with genotype data and extracted pharmacogenomics relevant single nucleotide variant (SNV) alleles,… read more here.
Keywords: pharmacogenetic allele; variant frequencies; allele; population ... See more keywords