rs1554749322
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces threonine with asparagine at codon 300 of the MUSK protein (p.Thr300Asn). The threonine residue is highly conserved and there is a small physicochemical difference between threonine and asparagine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with MUSK-related disease. Algorithms developed to predict the effect of missense changes on protein structure and function do not agree on the potential impact of this missense change (SIFT: "Tolerated"; 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
9
Location
110747786
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.899C>A (p.Thr300Asn)
Allele
A
Clinical Significance
Uncertain significance
Name
NM_005592.4(MUSK):c.899C>T (p.Thr300Ile)
Allele
T
Clinical Significance
Uncertain significance