ClinVar Miner

Submissions for variant NM_030930.4(UNC93B1):c.1350G>T (p.Lys450Asn)

gnomAD frequency: 0.00001  dbSNP: rs1134108
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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 RCV002031278 SCV002316123 uncertain significance Herpes simplex encephalitis, susceptibility to, 1 2020-12-21 criteria provided, single submitter clinical testing 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals with UNC93B1-related conditions. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database. This sequence change replaces lysine with asparagine at codon 450 of the UNC93B1 protein (p.Lys450Asn). The lysine residue is highly conserved and there is a moderate physicochemical difference between lysine and asparagine.

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