IthaID: 3674
Names and Sequences
| Functionality: | Globin gene causative mutation | Pathogenicity: | Variant of Uncertain Significance |
|---|---|---|---|
| Common Name: | -63 A>G | HGVS Name: | HBB:c.-113A>G |
| Hb Name: | N/A | Protein Info: | N/A |
Context nucleotide sequence:
AGCCACACCCTAGGGTTGGCCAATCTACTCCC [A/G] GGAGCAGGGAGGGCAGGAGCCAGGGCTGGG (Strand: -)
Also known as:
Comments: Found in a 16-year old Chinese male with normal hematological presentation and only slightly increased Hb A2 levels (3.7%).
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: | 70482 |
| Size: | 1 bp |
| Located at: | β |
| Specific Location: | Promoter |
Other details
| Type of Mutation: | Point-Mutation(Substitution) |
|---|---|
| Effect on Gene/Protein Function: | N/A |
| 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To the best of our knowledge, this is unpublished data.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 | Mohd Yasin, Norafiza | 2020-10-20 | First report. |
Created on 2020-10-23 11:11:52,
Last reviewed on 2020-10-27 11:17:31 (Show full history)
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