RHD*602G,667G,744T,957A,1025C,1063A
(ISBT table: not listed)
This entry is an RHD allele.
RHD(T201R,F223V,I342T,G355S), RHD(T201R,F223V,S248S,V319V,I342T,G355S), RHD(c.602G, c.667G, c.744T, c.957A, c.1025C, c.1063A), RHD*602C>G,667T>G,744C>T,957G>A,1025T>C,1063G>A, RHD*602G,667G,744T,957A,1025C,1063A,
Molecular data
Nucleotides:
602C>G; 667T>G; 744C>T; 957G>A; 1025T>C; 1063G>A;
Amino acids: T201R; F223V; S248S; V319V; I342T; G355S;
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: (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: Aug. 15, 2020)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: rare descriptions, Brazilian (last update: Dec. 22, 2019)Structure mapping
Movement | Mouse Input | Touch Input | ||
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Translation | Middle Mouse Button or Ctrl+Primary | Triple touch | ||
Zoom | Scroll Wheel or Second Mouse Button or Shift+Primary | Pinch (double touch) | ||
Slab | Ctrl+Second | Not Available |
References
- Arnoni CP et al. Identification of four novel RHD alleles with altered expression of D in Brazilians. Transfusion, 2016. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: May 14, 2019