RHD*1154-1C
(ISBT table: not listed)
This entry is an RHD allele.
RHD*1154-1C, RHD*1154-1C (IVS8-1C), RHD*1154-1G>C,
Molecular data
Nucleotides:
intronic 149G>C; intronic 486T>C; intronic 486G>A; intronic 1154G>C;
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
- no mutations were found by sequencing in all 10 RHD exons
- Table 6; 149-29G>C is an intronic polymorphism present in all samples with R1, R0 and RZ haplotypes
- Table 4; 486+117T>C and 486+124G>A are intronic polymorphisms present in all samples tested
Extracellular position of one or more amino acid substitutions:
- Silent or intronic mutations: none of the mutations are predicted to affect an extracellular amino acid.
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: D negative (DEL excluded?) (last update: July 28, 2020)Reports by D phenotype
Other RH phenotypes: RH:
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: unknown (last update: Dec. 9, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: D negative, at risk for anti-D (last update: Aug. 25, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: not expected, see phenotype data
Reports
Summary: exceptional description(s), Korean (last update: Dec. 22, 2019)Structure mapping
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References
- Seo MH et al. An effective diagnostic strategy for accurate detection of RhD variants including Asian DEL type in apparently RhD-negative blood donors in Korea. Vox Sang, 2016. [Citation] [RHeference]
- Tounsi WA et al. Complete RHD next-generation sequencing: establishment of reference RHD alleles. Blood Adv, 2018. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Aug. 15, 2019