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The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype.

Transfusion - 1 Aug 2024

Zhu Yuli, Qiu Caixia, Wang Yulin, Feng Zhihui

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Share to Amino Acid Substitution
Share to Mutation, Missense
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Share to Rh-Hr Blood-Group System

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Identifiers

PMID: 38856398
DOI: 10.1111/trf.17919

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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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The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype.PMID 38856398Read ↗

An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.Semantic proximity Read ↗

Identification of a novel missense mutation (p.Ser230Asn) in RHD allele in a Chinese individual with partial D phenotype.Semantic proximity Read ↗

Identification of a novel c.94dupA mutation in RHD allele.Semantic proximity Read ↗

A novel missense mutation (c.221G>C) in RHD gene identified in a Chinese woman.Semantic proximity Read ↗

A novel RHD allele, RHD c.56C>G (p.Thr19Arg), with Del phenotype identified in a Chinese family.Semantic proximity Read ↗

Novel RHD allele with c.333C>G change predicted to encode p.Phe111Leu.Semantic proximity Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

A novel RHD (c.509T>G, p.Met170Arg) allele shows weakened D expression.Semantic proximity Read ↗

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman.Semantic proximity Read ↗

A novel RHD allele caused by c.687_689delAAG variant.Semantic proximity Read ↗

A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual.Semantic proximity Read ↗

A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family.Semantic proximity Read ↗

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