rs373381192
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces glycine, which is neutral and non-polar, with serine, which is neutral and polar, at codon 153 of the LTBP3 protein (p.Gly153Ser). This variant is present in population databases (rs373381192, gnomAD 0.07%). This variant has not been reported in the literature in individuals affected with LTBP3-related conditions. ClinVar contains an entry for this variant (Variation ID: 464027). 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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. 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
C
Alternative Allele
G
T
Chromosome
11
Location
65554255
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.457G>A (p.Gly153Ser)
Allele
T
Clinical Significance
Uncertain significance