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Article

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

Transfusion - 1 Sept 2020

Chi Xiaoyun, Liu Li, Feng Zhihui, Zhang Shaoqiang

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Share to ABO Blood-Group System
Share to Alleles
Share to Amino Acid Substitution
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation, Missense

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Identifiers

PMID: 32671839
DOI: 10.1111/trf.15957

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.PMID 32671839Read ↗

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 a novel A allele with a c.36-39delA on the ABO*A1.02 allele.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 ↗

Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of novel variant B alleles within the ABO gene.Semantic proximity Read ↗

Identification of a novel A allele with a c.421T>C variant on the ABO*A1.02 allele in a Chinese individual.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 ↗

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

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