ClinVar Miner

Submissions for variant NM_024782.3(NHEJ1):c.259G>A (p.Ala87Thr)

gnomAD frequency: 0.00024  dbSNP: rs150307533
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001038603 SCV001202082 uncertain significance Cernunnos-XLF deficiency 2023-12-18 criteria provided, single submitter clinical testing This sequence change replaces alanine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 87 of the NHEJ1 protein (p.Ala87Thr). This variant is present in population databases (rs150307533, gnomAD 0.08%). This variant has not been reported in the literature in individuals affected with NHEJ1-related conditions. ClinVar contains an entry for this variant (Variation ID: 837303). 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 NHEJ1 protein function with a negative 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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