Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002537179 | SCV000944458 | uncertain significance | Blau syndrome; Regional enteritis | 2021-07-19 | criteria provided, single submitter | clinical testing | This variant has not been reported in the literature in individuals with NOD2-related disease. This variant is not present in population databases (ExAC no frequency). This sequence change replaces threonine with asparagine at codon 424 of the NOD2 protein (p.Thr424Asn). The threonine residue is highly conserved and there is a small physicochemical difference between threonine and asparagine. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). 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. |