IthaID: 3999
Names and Sequences
| Functionality: | Disease modifying mutation | Pathogenicity: | N/A |
|---|---|---|---|
| Common Name: | rs9315599 | HGVS Name: | NC_000013.11:g.20463469C>G |
Context nucleotide sequence:
CTCTAAAGGAAGCCAACCAGCATAA [C>G] AGTCCCAATGACTTCTGTCTCATGAG (Strand: +)
Also known as:
Comments: Associated with an increased risk of proteinuria in sickle cell disease cohorts (n 516 OMG-SCD, n 461 WalkPHaSST).
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: | Proteinuria [HP:0000093] |
Other details
| Type of Mutation: | Point-Mutation(Substitution) |
|---|---|
| Effect on Gene/Protein Function: | N/A |
| Ethnic Origin: | N/A |
| Molecular mechanism: | N/A |
| Inheritance: | Quantitative trait |
| DNA Sequence Determined: | Yes |
In silico pathogenicity prediction
Publications / Origin
- Garrett ME, Soldano KL, Erwin KN, Zhang Y, Gordeuk VR, Gladwin MT, Telen MJ, Ashley-Koch AE, Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy., Blood Adv, 2022
Created on 2023-01-17 14:52:11,
Last reviewed on 2023-01-17 14:53:23 (Show full history)
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