IthaID: 4011



Names and Sequences

Functionality: Globin gene causative mutation Pathogenicity: N/A
Common Name: CD 9 AAC>TAC [Asn>Tyr] HGVS Name: HBA2:c.28A>T
Hb Name: N/A Protein Info: N/A

Context nucleotide sequence:
GTGCTGTCTCCTGCCGACAAGACC [A>T] ACGTCAAGGCCGCCTGGGGTAAG (Strand: +)

Protein sequence:
MVLSPADKTYVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPAVHASLDKFLASVSTVLTSKYR

Also known as:

Comments: Found in a girl with the features of microcytosis and hypochromasia. HbA2 level of 2.93%; no abnormal hemoglobin detected using cellulose acetate electrophoresis. Sequence variation is absent from gnomADv2.1.1.

We follow the HGVS sequence variant nomenclature and IUPAC standards.

External Links

No available links

Phenotype

Hemoglobinopathy Group: Thalassaemia
Hemoglobinopathy Subgroup: α-thalassaemia
Allele Phenotype:N/A
Associated Phenotypes: N/A

Location

Chromosome: 16
Locus: NG_000006.1
Locus Location: 33803
Size: 1 bp
Located at: α2
Specific Location: Exon 1

Other details

Type of Mutation: Point-Mutation(Substitution)
Effect on Gene/Protein Function: Missense codons (Protein Structure)
Ethnic Origin: Chinese
Molecular mechanism: N/A
Inheritance: Recessive
DNA Sequence Determined: Yes

In silico pathogenicity prediction

Sequence Viewer

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Publications / Origin

  1. Yao XY, Yu J, Chen SP, Xiao JW, Zheng QC, Liu HY, Zhang L, Xian Y, Zou L, Prevalence and genetic analysis of α-thalassemia and β-thalassemia in Chongqing area of China., Gene , 532(1), 120-4, 2013 PubMed
Created on 2023-01-26 11:14:24, Last reviewed on (Show full history)

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