Article
High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype. Dezan MR, Oliveira VB, Gomes ÇN, Luz F, Gallucci AJ, Bonifácio SL, Alencar CS, Sabino EC, Pereira AC, Krieger JE, Rocha V, Mendrone-Junior A, Dinardo CL. J Clin Lab Anal, 2018. [Citation]
Annotations by Allele
- apparently deleted RHD with unexpected serology: Prevalence
- apparently deleted RHD with unexpected serology: Prevalence
- RHD deletion (RHD*01N.01): otherHaplotype (in trans to other alleles)
- RHD deletion (RHD*01N.01): otherHaplotype (in trans to other alleles)
- RHD deletion (RHD*01N.01): otherHaplotype (in trans to other alleles)
- RHD deletion (RHD*01N.01): otherHaplotype (in trans to other alleles)
- RHD or DIIIa-CEVS(4-7)-D - partly characterized or subtypes not separated: otherHaplotype
- RHD*1154C (weak D type 2): otherHaplotype
- RHD*1154C (weak D type 2): otherHaplotype
- RHD*1154C (weak D type 2): otherHaplotype
- RHD*1154C (weak D type 2): Prevalence
- RHD*1154C (weak D type 2): Prevalence
- RHD*1154C (weak D type 2): RH1
- RHD*157T (weak D type 104): RH1
- RHD*157T (weak D type 104): otherHaplotype
- RHD*157T (weak D type 104): Prevalence
- RHD*361A,380C,383G,455C (DIIIc): RH1
- RHD*361A,380C,383G,455C (DIIIc): otherHaplotype
- RHD*361A,380C,383G,455C (DIIIc): Prevalence
- RHD*446A (weak D type 5): RH1
- RHD*446A (weak D type 5): Prevalence
- RHD*446A (weak D type 5): otherHaplotype
- RHD*505C,509G,514T (DFR1, RHD*17.01): RH1
- RHD*505C,509G,514T (DFR1, RHD*17.01): otherHaplotype
- RHD*505C,509G,514T (DFR1, RHD*17.01): Prevalence
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): RH1
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): otherHaplotype
- RHD*602G,667G,819A (weak D type 4.0, DAR3.01): Prevalence
- RHD*635A (weak D type 112): otherHaplotype
- RHD*635A (weak D type 112): Prevalence
- RHD*802-41_802-38delCTCT,1157A (L386*, RHD*01N.58): otherHaplotype
- RHD*802-41_802-38delCTCT,1157A (L386*, RHD*01N.58): Prevalence
- RHD*802-41_802-38delCTCT,1157A (L386*, RHD*01N.58): RH1
- RHD*809G (weak D type 1): RH1
- RHD*809G (weak D type 1): otherHaplotype
- RHD*809G (weak D type 1): otherHaplotype
- RHD*809G (weak D type 1): otherHaplotype
- RHD*809G (weak D type 1): otherHaplotype
- RHD*809G (weak D type 1): Prevalence
- RHD*809G (weak D type 1): Prevalence
- RHD*833A (weak D type 38): Prevalence
- RHD*833A (weak D type 38): otherHaplotype
- RHD*833A (weak D type 38): RH1
- RHD*833A (weak D type 38): otherHaplotype
- RHD*833A (weak D type 38): otherHaplotype
- RHD*845A (weak partial D type 15): RH1
- RHD*845A (weak partial D type 15): otherHaplotype
- RHD*845A (weak partial D type 15): Prevalence
- RHD*845A (weak partial D type 15): otherHaplotype
- RHD*885T (weak partial D type 11): Prevalence
- RHD*885T (weak partial D type 11): RH1
- RHD*885T (weak partial D type 11): otherHaplotype
- RHD*8G (weak D type 3): Prevalence
- RHD*8G (weak D type 3): RH1
- RHD*8G (weak D type 3): otherHaplotype
- RHD*8G (weak D type 3): Prevalence
- RHD*D-cE(4-5)-D (DVI type 1): RH1
- RHD*D-cE(4-5)-D (DVI type 1): Prevalence
- RHD*D-cE(4-5)-D (DVI type 1): otherHaplotype
- RHD*DIIIa-CEVS(4-7)-D (RHD*03N.01): Prevalence
- RHD*Dpsi (RHD*08N.01): otherHaplotype
- RHD*Dpsi (RHD*08N.01): otherHaplotype
- RHD*Dpsi (RHD*08N.01): Prevalence
- RHD*Dpsi (RHD*08N.01): Prevalence
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: otherHaplotype
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: Prevalence
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: Prevalence
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: RH1
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: otherHaplotype
- weak D type 4.2.x (DAR) - partly characterized or subtypes not separated: otherHaplotype