rs1665660543
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces asparagine with aspartic acid at codon 76 of the SOX11 protein (p.Asn76Asp). The asparagine residue is highly conserved and there is a small physicochemical difference between asparagine and aspartic acid. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with SOX11-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: "Probably Damaging"; Align-GVGD: "Class C0"). 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
5692947
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.226A>G (p.Asn76Asp)
Allele
G
Clinical Significance
Uncertain significance