RHD*636T
(ISBT table: not listed)
				This entry is an RHD allele.
						DUC-1, RHD(G212G), RHD*636C>T, RHD*636T, RHD*636T (DUC1), 
					
	
				Molecular data
						Nucleotides:
						636C>T; 
					
Amino acids: G212G;
						Hybrid allele encompassing at least one  RHCE  exon:
						no
					
						Comments on the molecular basis:
						
						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:
						
- effect on splicing considered unlikely
 - effect on splicing predicted in silico
 - effect on splicing considered unlikely because of the normal phenotype of RBCs
 
						Unconventional prediction methods:
						
Phenotype
Main D phenotype: D positive (last update: Nov. 11, 2019)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: 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: exceptional description(s), in the German population (last update: Dec. 22, 2019)Structure mapping
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References
- Wagner FF et al. The DAU allele cluster of the RHD gene. Blood, 2002. [Citation] [RHeference]
 - Chen Q et al. Random survey for RHD alleles among D+ European persons. Transfusion, 2005. [Citation] [RHeference]
 - Flegel WA et al. Six years' experience performing RHD genotyping to confirm D- red blood cell units in Germany for preventing anti-D immunizations. Transfusion, 2009. [Citation] [RHeference]
 - Fichou Y et al. Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh. Transfusion, 2015. [Citation] [RHeference]
 - Chun S et al. The synonymous nucleotide substitution RHD 1056C>G alters mRNA splicing associated with serologically weak D phenotype. J Clin Lab Anal, 2018. [Citation] [RHeference]
 - Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
 
Last update: Dec. 20, 2019