Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003556032 | SCV004292865 | uncertain significance | not provided | 2023-11-25 | criteria provided, single submitter | clinical testing | This sequence change replaces arginine, which is basic and polar, with histidine, which is basic and polar, at codon 477 of the NR3C1 protein (p.Arg477His). This variant is present in population databases (rs104893913, gnomAD 0.0009%). This missense change has been observed in individual(s) with primary cortisol resistance (PMID: 11589680). ClinVar contains an entry for this variant (Variation ID: 16156). An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. Experimental studies have shown that this missense change affects NR3C1 function (PMID: 11589680, 15017388). This variant disrupts the p.Arg477 amino acid residue in NR3C1. Other variant(s) that disrupt this residue have been observed in individuals with NR3C1-related conditions (PMID: 11589680, 27120390, 29444898), which suggests that this may be a clinically significant amino acid residue. 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. |
OMIM | RCV000017539 | SCV000037811 | pathogenic | Glucocorticoid resistance | 2005-06-01 | no assertion criteria provided | literature only |