RHD*602G,667G,697C,733C,744T,1136T
(ISBT table: not listed)
This entry is an RHD allele.
RHD(T201R,F223V,E233Q,V245L,S248S,T379M), RHD(T201R,F223V,E233Q,V245L,T379M), RHD*602C>G,667T>G,697G>C,733G>C,744C>T,1136C>T, RHD*602G,667G,697C,733C,744C,1136T with a typo, RHD*602G,667G,697C,733C,744T,1136T, RHD*602G,667G,697C,733C,744T,1136T (DAU),
Molecular data
Nucleotides:
602C>G; 667T>G; 697G>C; 733G>C; 744C>T; 1136C>T;
Amino acids: T201R; F223V; E233Q; V245L; S248S; T379M;
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: variable/discrepant (last update: Dec. 10, 2020)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: Nov. 11, 2019)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, on the American continents (last update: Dec. 10, 2020)Structure mapping
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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]
- Jessica Keller et al. A Novel RHD Variant Identified in Two Pregnant Women with D Typing Discrepancies Transfusion, 2020. — Abstract — [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Dec. 10, 2020