Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002000544 | SCV002262648 | uncertain significance | not provided | 2021-09-20 | 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: "Tolerated"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals affected with OTOG-related conditions. This variant is present in population databases (rs754033112, ExAC 0.01%). This sequence change replaces asparagine with lysine at codon 2852 of the OTOG protein (p.Asn2852Lys). The asparagine residue is highly conserved and there is a moderate physicochemical difference between asparagine and lysine. |
Revvity Omics, |
RCV003130652 | SCV003816539 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 18B | 2019-02-28 | criteria provided, single submitter | clinical testing |