ClinVar Miner

Submissions for variant NM_145725.3(TRAF3):c.730A>T (p.Thr244Ser)

gnomAD frequency: 0.00009  dbSNP: rs149327017
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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 RCV001203219 SCV001374371 uncertain significance Herpes simplex encephalitis, susceptibility to, 3 2023-07-17 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. This sequence change replaces threonine, which is neutral and polar, with serine, which is neutral and polar, at codon 244 of the TRAF3 protein (p.Thr244Ser). This variant is present in population databases (rs149327017, gnomAD 0.02%). This variant has not been reported in the literature in individuals affected with TRAF3-related conditions. ClinVar contains an entry for this variant (Variation ID: 934763). 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 disruptive.

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