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Article

A new missense variant c.278C > G on the ABO*B.01 allele associated with a Bel phenotype.

Transfusion - 1 Apr 2023

He Yunlei, Deng Gang, Yu Lu, Shen Longqiang, Zhang Jiwei

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Share to ABO Blood-Group System
Share to Alleles
Share to Genotype
Share to Mutation, Missense

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 36799017
DOI: 10.1111/trf.17289

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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A new missense variant c.278C > G on the ABO*B.01 allele associated with a Bel phenotype.PMID 36799017Read ↗

The novel missense variant c.350G>T on the ABO*B.01 allele associated with a Bel phenotype.Semantic proximity Read ↗

Identification of a novel missense mutation (563G>a) in the ABO gene associated with a Bel phenotype.Semantic proximity Read ↗

c.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype.Semantic proximity Read ↗

A novel c.29-3C>G variant on the B allele forms the Bel phenotype.Semantic proximity Read ↗

Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.Semantic proximity Read ↗

Identification of a novel B allele with a c.586T>C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel A allele with c.478C>T missense mutation on the ABO*A1.02 background.Semantic proximity Read ↗

c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype.Semantic proximity Read ↗

Identification of a novel A allele with a c.423 C > A mutation on the ABO*A1.02 allele.Semantic proximity Read ↗

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.Semantic proximity Read ↗

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.Semantic proximity Read ↗

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