rs751857347
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces arginine with glutamine at codon 41 of the RPS24 protein (p.Arg41Gln). The arginine residue is highly conserved and there is a small physicochemical difference between arginine and glutamine. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the ExAC database. This variant has not been reported in the literature in individuals affected with RPS24-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C35"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78035563
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.122G>A (p.Arg41Gln)
Allele
A
Clinical Significance
Uncertain significance