rs1557179679
- Uncertain significance
Your Genotype
Sign InDescription
A variant of uncertain significance has been identified in the FLNA gene. The T143I variant has not been published as pathogenic or been reported as benign to our knowledge. This variant is not observed in large population cohorts (Lek et al., 2016). The T143I variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved across species, and in silico analysis predicts this variant is probably damaging to the protein structure/function. However, this variant lacks observation in a significant number of affected individuals, segregation data, and functional evidence, which would further clarify its pathogenicity.
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154368036
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001110556.2(FLNA):c.428C>T (p.Thr143Ile)
Allele
A
Clinical Significance
Uncertain significance