RHD*594T,602G,667G,819A
(ISBT table: not listed)
This entry is an RHD allele.
RHD(K198N,T201R,F223V), RHD(K198N,T201R,F223V,A273A), RHD*594A>T,602C>G,667T>G,819G>A, RHD*594T,602G,667G,819A, RHD*594T,602G,667G,819A (weak D type 4.4), weak D type 4.4,
Molecular data
Nucleotides:
594A>T; 602C>G; 667T>G; 819G>A;
Amino acids: K198N; T201R; F223V; A273A;
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
- see also "Additional comments" section on the RhesusBase http://www.rhesusbase.info/RHDRHD(K198N,T201R,F223V,A273A).htm
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: weak D (last update: Nov. 17, 2019)Reports by D phenotype
Other RH phenotypes: RH:-2, -3,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: ce (last update: Jan. 8, 2021)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Nov. 17, 2019)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), French Afro-Caribbean (last update: Dec. 22, 2019)Detailed reports
- 1 sample Afro-Caribbean, in the French population
- 1 sample? in the French population (KX216809)
- 1 hemizygote among 278 samples selected for the development of nonspecific quantitative next-generation sequencing. (non-random samples, may have been reported in other studies)
Allele or phenotype frequency
Structure mapping
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References
- Wagner FF and Flegel WA et al. The Human RhesusBase Online ressource, 2011. — Online ressource — [RHeference]
- Floch A et al. Molecular characterization of 13 new RHD alleles. Transfusion, 2017. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
- Stef M et al. RH genotyping by nonspecific quantitative next-generation sequencing. Transfusion, 2020. [Citation] [RHeference]
Last update: Jan. 8, 2021