IthaID: 3540
Names and Sequences
| Functionality: | Disease modifying mutation | Pathogenicity: | N/A |
|---|---|---|---|
| Common Name: | rs1482813291 | HGVS Name: | NC_000010.11:g.70151276_70151284del |
Context nucleotide sequence:
TTCATACCAAAAAAAAAAAAAAAA [-/AAAAAAAAA] CCTGGAAAAGCTACAGATGTTAACC (Strand: +)
Also known as:
Comments: Variant showed significant association with total haemoglobin levels after hydroxyurea treatment in SCD patients. Source: Blood (2019) 134 (Supplement_1): 987; doi.org/10.1182/blood-2019-124965.
We follow the HGVS sequence variant nomenclature and IUPAC standards.
External Links
Phenotype
| Allele Phenotype (Cis): | N/A |
|---|---|
| Allele Phenotype (Trans): | N/A |
| Associated Phenotypes: | Response to hydroxyurea |
Location
| Chromosome: | 10 |
|---|---|
| Locus: | NM_001142648.2 |
| Locus Location: | N/A |
| Size: | 9 bp |
| Located at: | SAR1A |
| Specific Location: | 3'UTR 0 |
Other details
| Type of Mutation: | Point-Mutation(Deletion) |
|---|---|
| Effect on Gene/Protein Function: | N/A |
| Ethnic Origin: | N/A |
| Molecular mechanism: | N/A |
| Inheritance: | N/A |
| DNA Sequence Determined: | No |
In silico pathogenicity prediction
Note:
The impact thresholds provided in this section are based on the analyses performed in Tamana et.al. For any given tool, the impact thresholds defined for the set of variants with the same effect on function as the variant examined, are preferred over those defined for the full dataset.
Sequence Viewer
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Publications / Origin
To the best of our knowledge, this is unpublished data. Please use with caution!
Created on 2019-12-12 15:08:51,
Last reviewed on 2019-12-12 15:41:22 (Show full history)
| A/A | Date | Curator(s) | Comments |
|---|---|---|---|
| 1 | 2019-12-12 15:08:51 | The IthaGenes Curation Team | Created |
| 2 | 2019-12-12 15:41:22 | The IthaGenes Curation Team | Reviewed. Locus added. |
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IthaGenes was last updated on 2024-11-20 13:24:07