Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000794413 | SCV000933818 | uncertain significance | Fanconi anemia | 2022-12-31 | 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"). ClinVar contains an entry for this variant (Variation ID: 641222). This variant has not been reported in the literature in individuals affected with FANCM-related conditions. This variant is present in population databases (rs772477865, gnomAD 0.05%). This sequence change replaces valine, which is neutral and non-polar, with isoleucine, which is neutral and non-polar, at codon 990 of the FANCM protein (p.Val990Ile). |
Fulgent Genetics, |
RCV002501045 | SCV002778468 | uncertain significance | Spermatogenic failure 28; Premature ovarian failure 15 | 2021-08-16 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV004619414 | SCV005113464 | likely benign | Inborn genetic diseases | 2024-03-21 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |