Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000792578 | SCV000931883 | uncertain significance | Fanconi anemia | 2018-12-05 | criteria provided, single submitter | clinical testing | This variant has not been reported in the literature in individuals with FANCM-related conditions. 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 tolerated, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant is present in population databases (rs548726090, ExAC 0.06%). This sequence change replaces proline with leucine at codon 41 of the FANCM protein (p.Pro41Leu). The proline residue is weakly conserved and there is a moderate physicochemical difference between proline and leucine. |