Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001937425 | SCV002134061 | uncertain significance | 46,XY sex reversal 6 | 2021-02-03 | criteria provided, single submitter | clinical testing | This sequence change replaces serine with leucine at codon 1472 of the MAP3K1 protein (p.Ser1472Leu). The serine residue is highly conserved and there is a large physicochemical difference between serine and leucine. 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C25"). This variant has not been reported in the literature in individuals with MAP3K1-related conditions. This variant is present in population databases (rs776167103, ExAC 0.009%). |