Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000631238 | SCV000752260 | uncertain significance | Wilson disease | 2017-09-17 | 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. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has been reported as homozygous in an individual affected with Wilson disease (PMID: 10502777). This variant is not present in population databases (ExAC no frequency). This sequence change replaces threonine with alanine at codon 1033 of the ATP7B protein (p.Thr1033Ala). The threonine residue is highly conserved and there is a small physicochemical difference between threonine and alanine. |