rs754730206
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces arginine, which is basic and polar, with cysteine, which is neutral and slightly polar, at codon 668 of the MUSK protein (p.Arg668Cys). This variant is present in population databases (rs754730206, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with MUSK-related conditions. ClinVar contains an entry for this variant (Variation ID: 476139). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt MUSK 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
C
Alternative Allele
T
Chromosome
9
Location
110800380
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2002C>T (p.Arg668Cys)
Allele
T
Clinical Significance
Uncertain significance