rs1405712076
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces alanine with serine at codon 1782 of the TSC2 protein (p.Ala1782Ser). The alanine residue is weakly conserved and there is a moderate physicochemical difference between alanine and serine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with TSC2-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The serine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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
T
Chromosome
16
Location
2088530
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_000548.5(TSC2):c.5344G>T (p.Ala1782Ser)
Allele
T
Clinical Significance
Uncertain significance