Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001227462 | SCV001399823 | uncertain significance | not provided | 2022-09-19 | 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 829829). This variant has not been reported in the literature in individuals affected with WHRN-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces arginine, which is basic and polar, with proline, which is neutral and non-polar, at codon 55 of the WHRN protein (p.Arg55Pro). |
Bioscientia Institut fuer Medizinische Diagnostik Gmb |
RCV001029765 | SCV001192543 | uncertain significance | Usher syndrome type 2D | 2019-04-08 | no assertion criteria provided | clinical testing |