ClinVar Miner

Submissions for variant NM_006087.4(TUBB4A):c.1213G>A (p.Glu405Lys)

dbSNP: rs745756691
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001930200 SCV002133099 uncertain significance Hypomyelinating leukodystrophy 6 2024-02-24 criteria provided, single submitter clinical testing This sequence change replaces glutamic acid, which is acidic and polar, with lysine, which is basic and polar, at codon 405 of the TUBB4A protein (p.Glu405Lys). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with TUBB4A-related conditions. This missense change has been observed in at least one individual who was not affected with TUBB4A-related conditions (Invitae). ClinVar contains an entry for this variant (Variation ID: 1366727). 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 TUBB4A protein function with a positive predictive value of 80%. 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.

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