IthaID: 548

Names and Sequences

Functionality: Globin gene causative mutation Pathogenicity: Benign / Likely Benign
Common Name: CD 49 AGC>AGA or AGG [Ser>Arg] HGVS Name: HBA2:c.150C>A |HBA2:c.150C>G
Hb Name: Hb Savaria Protein Info: α2 49(CE7) Ser>Arg

Context nucleotide sequence:

Protein sequence:

Also known as:

We follow the HGVS sequence variant nomenclature and IUPAC standards.


Hemoglobinopathy Group: Structural Haemoglobinopathy
Hemoglobinopathy Subgroup: α-chain variant
Allele Phenotype:N/A
Stability: N/A
Oxygen Affinity: N/A
Associated Phenotypes: N/A


Chromosome: 16
Locus: NG_000006.1
Locus Location: 34042
Size: 1 bp
Located at: α2
Specific Location: Exon 2

Other details

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

In silico pathogenicity prediction

Sequence Viewer

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Publications / Origin

  1. Szelényi JG, Horányi M, Földi J, Hudacsek J, István L, Hollán SR, A new hemoblogin variant in hungary: Hb Savaria - alpha 49 (CE7) Ser replace by Arg., Hemoglobin , 4(1), 27-38, 1980 PubMed
  2. Juricić D, Efremov GD, Wilson JB, Huisman TH, Hb Savaria or alpha(2)49(CE7)Ser----Arg beta 2 in a Yugoslavian family., Hemoglobin , 9(6), 631-3, 1985 PubMed
  3. Zhang H, Li C, Li J, Hou S, Chen D, Yan H, Chen S, Liu S, Yin Z, Yang X, Tan J, Huang X, Zhang L, Fang J, Zhang C, Li W, Guo J, Lei D, Next-generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China., J Clin Lab Anal, 33(4), e22845, 2019 PubMed
Created on 2010-06-16 16:13:15, Last reviewed on 2021-01-30 12:37:13 (Show full history)

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