Varaico: Literature-Extracted Genetic Variants

Gene:RHCE
Variant:p.V223F
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RHCE

NM_020485.8:p.V223F

Associated Papers

A novel RHCE*ce(c.48C)-D(4)-ce allele in a family of African ancestry.

Tournamille C et al.

Transfusion, 2025

First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.

Mbeti JMM et al.

Blood Transfusion = Trasfusione Del Sangue, 2024

Machine learning to optimize automated RH genotyping using whole-exome sequencing data.

Chang TC et al.

Blood Advances, 2024

38522094 (PubMed )
Supplement: BLOODA_ADV-2023-011660-mmc1.xlsx › Rh

Serological screening and genetic analysis of RhCE variants in the Chinese Southern Han donors.

Jia S et al.

Transfusion Medicine (oxford, England), 2021

Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors.

Dezan MR et al.

Transfusion, 2021

Molecular Blood Group Screening in Donors from Arabian Countries and Iran Using High-Throughput MALDI-TOF Mass Spectrometry and PCR-SSP.

Flesch BK et al.

Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020

A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.

Chang TC et al.

Blood Advances, 2020

Next-Generation Sequencing Technologies in Blood Group Typing.

Fürst D et al.

Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020

Genotyping of 28 blood group alleles in blood donors from Mali: Prediction of rare phenotypes.

Ba A et al.

Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2016

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).

Storry JR et al.

Vox Sanguinis, 2014

Systematic RH genotyping and variant identification in French donors of African origin.

Kappler-Gratias S et al.

Blood Transfusion = Trasfusione Del Sangue, 2014

RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.

Westhoff CM et al.

Transfusion, 2013

RHD*weak partial 4.0 is associated with an altered RHCE*ce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.

Ouchari M et al.

Transfusion Medicine (oxford, England), 2013

Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.

Silvy M et al.

British Journal of Haematology, 2011

Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease.

Pham BN et al.

Transfusion, 2011

Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.

Peyrard T et al.

Transfusion, 2009

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

RhCE protein variants in Southwestern Germany detected by serologic routine testing.

Bugert P et al.

Transfusion, 2009

Two new alleles of the RHCE gene in Black individuals: the RHce allele ceMO and the RHcE allele cEMI.

Noizat-Pirenne F et al.

British Journal of Haematology, 2001

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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."