IthaID: 92



Names and Sequences

Functionality: Globin gene causative mutation Pathogenicity: Pathogenic / Likely Pathogenic
Common Name: CD 27/28 (+C) HGVS Name: HBB:c.85dupC
Hb Name: N/A Protein Info: N/A

Context nucleotide sequence:
CGTGGATGAAGTTGGTGGTGAGGCCC [-/C] TGGGCAGGTTGGTATCAAGGTTAC (Strand: -)

Also known as:

We follow the HGVS sequence variant nomenclature and IUPAC standards.

Phenotype

Hemoglobinopathy Group: Thalassaemia
Hemoglobinopathy Subgroup: β-thalassaemia
Allele Phenotype:β0
Associated Phenotypes: Haemolytic anaemia [HP:0001878]
Ineffective erythropoiesis [HP:0010972]

Location

Chromosome: 11
Locus: NG_000007.3
Locus Location: 70679
Size: 1 bp
Located at: β
Specific Location: Exon 1

Other details

Type of Mutation: Point-Mutation(Insertion)
Effect on Gene/Protein Function: Frameshift (Translation)
Ethnic Origin: Chinese, Thai
Molecular mechanism: N/A
Inheritance: Recessive
DNA Sequence Determined: No

In silico pathogenicity prediction

Sequence Viewer

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Frequencies

Publications / Origin

  1. Cai SP, Chui DH, Ng J, Poon AO, Freedman MH, Olivieri NF, A new frameshift beta zero-thalassemia mutation (codons 27-28 +C) found in a Chinese family., American journal of hematology, 37(1), 6-8, 1991 PubMed
  2. Lin LI, Lin KS, Lin KH, Chang HC, The spectrum of beta-thalassemia mutations in Taiwan: identification of a novel frameshift mutation., American journal of human genetics, 48(4), 809-12, 1991 PubMed
Created on 2010-06-16 16:13:14, Last reviewed on 2019-11-12 13:04:38 (Show full history)

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