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ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.

Transfusion - 1 Sept 2021

Feng Chenchen, Li Hui, Liu Taixiang, Xiao Jianyu, Huang Chengyin, Flegel Willy A, Chen Qing

Abstract excerpt

No abstract is available from the source.

Topics

ABO Blood-Group System
Adult
Alleles
Amino Acid Substitution
Humans
Male
Mutation, Missense
Phenotype
Polymorphism, Single Nucleotide

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 34323306
DOI: 10.1111/trf.16597
PMCID: PMC9885333

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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Click a neighbor to travelStep 1 · 12 closest

ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.PMID 34323306Read ↗

Identification of a novel B allele with a nucleotide deletion (c.103_106 delG) in the ABO gene associated with a B weak phenotype.Semantic proximity Read ↗

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.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 B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.917 T > C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

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

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

Identification of a novel c.77T>G mutation on the ABO*B.01 allele associated with a B subtype.Semantic proximity Read ↗

Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel c.259G > T mutation in the ABO*B.01 allele giving rise to a B3 phenotype.Semantic proximity Read ↗

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