ClinVar Miner

Submissions for variant NM_003265.3(TLR3):c.1847A>C (p.Asn616Thr)

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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 RCV003069349 SCV003467316 uncertain significance Herpes simplex encephalitis, susceptibility to, 1 2023-03-19 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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant  is likely to be tolerated. ClinVar contains an entry for this variant (Variation ID: 2154568). This variant has not been reported in the literature in individuals affected with TLR3-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.002%). This sequence change replaces asparagine, which is neutral and polar, with threonine, which is neutral and polar, at codon 616 of the TLR3 protein (p.Asn616Thr).

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