Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Invitae | RCV000468713 | SCV000553166 | uncertain significance | Congenital contractural arachnodactyly | 2016-04-04 | criteria provided, single submitter | clinical testing | This sequence change replaces glycine with arginine at codon 630 of the FBN2 protein (p.Gly630Arg). The glycine residue is highly conserved and there is a moderate physicochemical difference between glycine and arginine. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a FBN2-related disease. 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: "Probably Damaging"; Align-GVGD: "Class C15"). In addition, algorithms developed to predict the effect of sequence changes on mRNA splicing suggest that this variant may alter mRNA splicing, but this prediction has not been confirmed by published transcriptional studies In summary, this variant is a novel missense change with uncertain impact on protein function and splicing. In the absence of functional or segregation data, at this time it has been classified as a Variant of Uncertain Significance. |