Nucleotides: 186G>T; 410C>T; 455A>C; 602C>G; 733G>C;

Amino acids: L62F; A137V; N152T; T201R; V245L;

Hybrid allele encompassing at least one RHCE exon: no

Comments on the molecular basis:

• In this study the presence or the absence of c.1136C>T could not be called accurately according to the authors. Data for this allele suggestive of Exon 9 either being deleted or deriving from RHCE. One heterozygous sample could be either RHef00792 with RHef00442 or RHef00058 with RHef00091.)
• The absence of c.819G>A p.A273A in these samples is not explicitely mentionned.

Extracellular position of one or more amino acid substitutions:

• none of the mutations are predicted to affect an extracellular amino acid

Splicing:

Unconventional prediction methods:

Reports by D phenotype

Other RH phenotypes: RH:

Serology with monoclonal anti-D

Antigen Density (Ag/RBC)

More phenotype data

Reports by CcEe phenotype

Reports by allele association

Antibodies in D negative recipients

Alloimmunization in recipients: unknown

Detailed reports

• 1/72 (+ potentially 1 heterozygous) random samples selected for whole genome sequencing Indigenous Australian community of Martu ancestry at the edge of the Western Desert, Western Australia

Allele or phenotype frequency