Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001046058 | SCV001209943 | uncertain significance | Holocarboxylase synthetase deficiency | 2021-08-26 | criteria provided, single submitter | clinical testing | This sequence change replaces proline with leucine at codon 47 of the HLCS protein (p.Pro47Leu). The proline residue is weakly conserved and there is a moderate physicochemical difference between proline and leucine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with HLCS-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The leucine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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. |
Natera, |
RCV001046058 | SCV002083748 | uncertain significance | Holocarboxylase synthetase deficiency | 2021-07-20 | no assertion criteria provided | clinical testing |