Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000638960 | SCV000760517 | uncertain significance | Familial melanoma | 2017-08-30 | 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 do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with CDK4-related disease. This variant is not present in population databases (ExAC no frequency). This sequence change replaces methionine with leucine at codon 75 of the CDK4 protein (p.Met75Leu). The methionine residue is moderately conserved and there is a small physicochemical difference between methionine and leucine. |