Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000195827 | SCV000255004 | uncertain significance | Hemochromatosis type 4 | 2015-03-30 | criteria provided, single submitter | clinical testing | This sequence change replaces histidine with arginine at codon 507 of the SLC40A1 protein (p.His507Arg). The histidine residue is highly conserved and there is a small physicochemical difference between histidine and arginine. This variant has been reported in the literature and is not present in population databases. This variant was reported in a patient affected with hepatocellular iron storage, hyperferritinemia, and increased transferrin saturation (PMID: 21396368). Segregation studies have not been reported for this variant. Experimental studies have shown that this missense change causes defective hepcidin binding in vitro and leads to hepcidin resistance (PMID: 21396368). Algorithms developed to predict the effect of missense changes on protein structure and function do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). In summary, this variant has been reported in an affected patient and experimental evidence have shown that this missense change disrupts ferroportin function. However, segregation studies have not been reported at this time. For these reasons, this change has been classified as a Variant of Uncertain Significance. |
Laboratory of Molecular Genetics and Genomics, |
RCV000195827 | SCV001445837 | uncertain significance | Hemochromatosis type 4 | 2020-07-01 | no assertion criteria provided | clinical testing |