Variants
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rs1603362434

  • Uncertain significance

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Description

Has not been previously published as pathogenic or benign to our knowledge; Not observed in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function

This sequence change replaces threonine, which is neutral and polar, with methionine, which is neutral and non-polar, at codon 608 of the FLNA protein (p.Thr608Met). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with FLNA-related conditions. ClinVar contains an entry for this variant (Variation ID: 661868). 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 not expected to disrupt FLNA 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

G


Alternative Allele

A

Chromosome

X


Location

154364826


Variant Type

SNP

Genes

ClinVar

Name

NM_001110556.2(FLNA):c.1823C>T (p.Thr608Met)


Allele

A


Clinical Significance

Uncertain significance

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