rs754254864
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces arginine, which is basic and polar, with tryptophan, which is neutral and slightly polar, at codon 732 of the SULF1 protein (p.Arg732Trp). This variant is present in population databases (rs754254864, gnomAD 0.02%). This variant has not been reported in the literature in individuals affected with SULF1-related conditions. ClinVar contains an entry for this variant (Variation ID: 282083). 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
C
Alternative Allele
A
T
Chromosome
8
Location
69629589
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.2194C>T (p.Arg732Trp)
Allele
T
Clinical Significance
Uncertain significance