rs1661264441
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces isoleucine with valine at codon 45 of the RPS7 protein (p.Ile45Val). The isoleucine residue is highly conserved and there is a small physicochemical difference between isoleucine and valine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with RPS7-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. 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
A
Alternative Allele
G
Chromosome
2
Location
3575874
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.133A>G (p.Ile45Val)
Allele
G
Clinical Significance
Uncertain significance