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Article

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

Transfusion - 1 Oct 2020

Kim Tae Yeul, Yu HongBi, Chung Yoo Na, Jang Ja-Hyun, Cho Duck

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

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32959374
DOI: 10.1111/trf.16033

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Research trail→

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The novel missense variant c.350G>T on the ABO*B.01 allele associated with a Bel phenotype.PMID 32959374Read ↗

A new missense variant c.278C > G 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 ↗

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.256G>A mutation on the ABO*B.01 allele.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 ↗

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 ↗

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

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