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Article

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

Transfusion - 1 Jan 2017

Ying Yanlin, Chen Shu, Ma Kairong, Hong Xiaozhen, Zhu Faming

Abstract excerpt

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Share to ABO Blood-Group System
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Share to ABO gene

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27774603
DOI: 10.1111/trf.13870

Genes

ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.PMID 27774603Read ↗

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 a c.586T>C 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 ↗

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

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

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

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 initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.Semantic proximity Read ↗

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