Variants
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rs2077843836

  • Uncertain significance

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Description

This sequence change replaces glutamic acid, which is acidic and polar, with valine, which is neutral and non-polar, at codon 569 of the MUSK protein (p.Glu569Val). This variant is not present in population databases (gnomAD no frequency). 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: 863070). 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

A


Alternative Allele

T

Chromosome

9


Location

110785646


Variant Type

SNP

Genes

ClinVar

Name

NM_005592.4(MUSK):c.1706A>T (p.Glu569Val)


Allele

T


Clinical Significance

Uncertain significance

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