IthaID: 3797
Names and Sequences
| Functionality: | Globin gene causative mutation | Pathogenicity: | N/A |
|---|---|---|---|
| Common Name: | IVS II-509 (-A) | HGVS Name: | HBB:c.316-342delA |
| Hb Name: | N/A | Protein Info: | N/A |
Context nucleotide sequence:
TTTGCATTTGTAATTTTAAAAA [A/-] TGCTTTCTTCTTTTAATATACTT (Strand: -)
Also known as:
Comments: Found in a 6-month-old Croatian girl presented with β-thalassemia minor.
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: | 71548 |
| Size: | 1 bp |
| Located at: | β |
| Specific Location: | Intron 2 |
Other details
| Type of Mutation: | Point-Mutation(Deletion) |
|---|---|
| Effect on Gene/Protein Function: | N/A |
| Ethnic Origin: | Croatian |
| Molecular mechanism: | N/A |
| Inheritance: | Recessive |
| DNA Sequence Determined: | Yes |
In silico pathogenicity prediction
Publications / Origin
- Vucak J, Turudic D, Milosevic D, Bilic M, Salek Z, Rincic M, Bilic E, Genotype-phenotype Correlation of β-Thalassemia in Croatian Patients: A Specific HBB Gene Mutations., J Pediatr Hematol Oncol, 40(2), e77-e82, 2018
Created on 2021-06-14 13:00:43,
Last reviewed on 2022-10-19 15:13:29 (Show full history)
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