rs201828504
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces arginine, which is basic and polar, with glutamine, which is neutral and polar, at codon 97 of the SAMD11 protein (p.Arg97Gln). This variant is present in population databases (rs201828504, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with SAMD11-related conditions. ClinVar contains an entry for this variant (Variation ID: 1047625). 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 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
G
Alternative Allele
A
Chromosome
1
Location
931074
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.827G>A (p.Arg276Gln)
Allele
A
Clinical Significance
Uncertain significance