IthaID: 3750
Names and Sequences
| Functionality: | Globin gene causative mutation | Pathogenicity: | N/A |
|---|---|---|---|
| Common Name: | CD 115 GCC>ACC [Ala>Thr] | HGVS Name: | HBB:c.346G>A |
| Hb Name: | N/A | Protein Info: | β 115(G17) Ala>Thr |
Context nucleotide sequence:
GGGCAACGTGCTGGTCTGTGTGCTG [G/A] CCCATCACTTTGGCAAAGAATTCAC (Strand: -)
Protein sequence:
MVHLTPEEKSAVTALWGKVNVDEVGGEALGRLLVVYPWTQRFFESFGDLSTPDAVMGNPKVKAHGKKVLGAFSDGLAHLDNLKGTFATLSELHCDKLHVDPENFRLLGNVLVCVLTHHFGKEFTPPVQAAYQKVVAGVANALAHKYH
Also known as:
Comments: Found in compound heterozygosity with the CD 41/42 (-CTTT) [IthaID: 147] in a 56-year old Chinese male presented with mild anaemia, microcytosis and hypochromia.
We follow the HGVS sequence variant nomenclature and IUPAC standards.
External Links
No available links
Phenotype
| Hemoglobinopathy Group: | Thalassaemia |
|---|---|
| Hemoglobinopathy Subgroup: | β-thalassaemia |
| Allele Phenotype: | N/A |
| Associated Phenotypes: | N/A |
Location
| Chromosome: | 11 |
|---|---|
| Locus: | NG_000007.3 |
| Locus Location: | 71920 |
| Size: | 1 bp |
| Located at: | β |
| Specific Location: | Exon 3 |
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
Publications / Origin
To the best of our knowledge, this is unpublished data. Please use with caution!
Microattributions
| A/A | Contributor(s) | Date | Comments |
|---|---|---|---|
| 1 | Li, Youqiong | 2020-11-25 | First report. |
Created on 2021-02-25 15:35:49,
Last reviewed on 2022-09-15 14:57:05 (Show full history)
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