MUTATION IVS-II-850 (G->A); 
       105         105
CAACAG^CTC->CAACAA^CTC
AMINO ACID REPLACEMENT None
TYPE OF BETA-THAL beta°
MECHANISM The G->A change in the AG dinucleotide which is required for normal splicing, abolishes this process, and no normal mRNA is produced
IDENTIFICATION Amplification of the beta-globin gene; DNA sequencing; dot-blot analysis with allele specific probes
HEMATOLOGY IN HETEROZYGOTE(S) Six members of the family; average values: Hb 12.0 g/dl; MCV 70 fl; MCH 21.2 pg; Hb A2 5.6%; Hb F 5.2%
HEMATOLOGY IN HOMOZYGOTE(S) Not reported
OCCURRENCE In a North European family living in the USA
HAPLOTYPE Not determined
FOUND IN COMBINATION WITH ABNORMAL HB(S) Not reported
FOUND IN COMBINATION WITH BETA-THAL ALLELE(S) Not reported
OTHER INFORMATION None
       
REFERENCES
1. Çürük, M.A., Howard, S.C., Kutlar, A., Huisman, T.H.J.: Hemoglobin, 19:207, 1995.

This material is from the book A Syllabus of Thalassemia Mutations (1997) by Titus H.J. Huisman, Marianne F.H. Carver, and Erol Baysal, published by The Sickle Cell Anemia Foundation in Augusta, GA, USA. Copyright © 1997 by Titus H.J. Huisman. All rights reserved. Neither this work nor any part may be reproduced or transmitted in any form or by any means, electronic or mechanical, microfilming and recording, or by any information storage and retrieval systems, without permission in writing from the Author.