Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001035091 | SCV001198406 | uncertain significance | X-linked agammaglobulinemia with growth hormone deficiency | 2019-01-16 | criteria provided, single submitter | clinical testing | This sequence change replaces cysteine with arginine at codon 506 of the BTK protein (p.Cys506Arg). The cysteine residue is moderately conserved and there is a large physicochemical difference between cysteine and arginine. This variant is not present in population databases (ExAC no frequency). This variant has been observed in an individual affected with X-linked agammaglobulinemia (PMID: 7880320). ClinVar contains an entry for this variant (Variation ID: 11376). 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 C15"). This variant disrupts the p.Cys506 amino acid residue in BTK. Other variant(s) that disrupt this residue have been observed in individuals with BTK-related conditions (PMID: 15661032, 9143921, 9445504, 10859027), suggesting that it is a clinically significant residue. As a result, variants that disrupt this residue are likely to be causative of disease. 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 | RCV000012129 | SCV000032363 | pathogenic | X-linked agammaglobulinemia | 1994-10-01 | no assertion criteria provided | literature only |