Varaico: Literature-Extracted Genetic Variants

Gene:RHD
Variant:p.A129T
Back to variants list

RHD

NM_016124.6:p.A129T

Associated Papers

Transfusion management of Africans with RHD variants in China.

Yin Q et al.

Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023

Performance evaluation of differential splicing analysis methods and splicing analytics platform construction.

Li K et al.

Nucleic Acids Research, 2022

35993808 (PubMed )
Supplement: gkac686_supplemental_files.zip › Table_S4_The_positive_and_negative_splicing_variants_benchmarker.xlsx › ROC

Molecular characterization of RhD variant phenotypes among blood donors: A study from the coastal region of India.

Polavarapu I et al.

Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2021

Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotype.

Raud L et al.

Transfusion, 2019

First description of a D-CE-D hybrid gene on a weak D Type 2 molecular background.

Granier T et al.

Transfusion, 2017

Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.

Fichou Y et al.

Transfusion, 2015

Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.

Silvy M et al.

Transfusion, 2011

RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.

Döscher A et al.

Transfusion, 2009

Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.

Körmöczi GF et al.

Transfusion, 2005

Random survey for RHD alleles among D+ European persons.

Chen Q et al.

Transfusion, 2005

Molecular characterization of weak D phenotypes by site-directed mutagenesis and expression of mutant Rh-green fluorescence protein fusions in K562 cells.

Kamesaki T et al.

Vox Sanguinis, 2001

RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis.

Legler TJ et al.

Transfusion Medicine (oxford, England), 2001

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."