Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003535608 | SCV002120902 | uncertain significance | Familial adenomatous polyposis 1 | 2015-12-16 | criteria provided, single submitter | clinical testing | In summary, this is a novel missense change that is not predicted to affect protein function or cause disease. However the evidence is insufficient at this time to prove that conclusively. 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. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a APC-related disease. This sequence change replaces proline with serine at codon 1101 of the APC protein (p.Pro1101Ser). The proline residue is moderately conserved and there is a moderate physicochemical difference between proline and serine. |
Baylor Genetics | RCV000231060 | SCV004200430 | uncertain significance | Familial adenomatous polyposis 1 | 2021-08-14 | criteria provided, single submitter | clinical testing |