Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Invitae | RCV000538491 | SCV000623645 | uncertain significance | Hypertrophic cardiomyopathy | 2021-06-14 | criteria provided, single submitter | clinical testing | This variant is found within a region of MYH7 between codons 181 and 937 that contains the majority of the myosin head domain. Missense variants in this region have been shown to be significantly overrepresented in individuals with hypertrophic cardiomyopathy (PMID: 27532257). 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 (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has been observed in individual(s) with hypertrophic cardiomyopathy (PMID: 27532257, 10521296). ClinVar contains an entry for this variant (Variation ID: 177669). This variant is not present in population databases (ExAC no frequency). This sequence change replaces glutamic acid with glycine at codon 499 of the MYH7 protein (p.Glu499Gly). The glutamic acid residue is highly conserved and there is a moderate physicochemical difference between glutamic acid and glycine. |
| Laboratory for Molecular Medicine, |
RCV000154260 | SCV000203915 | uncertain significance | not specified | 2013-02-14 | no assertion criteria provided | clinical testing | proposed classification - variant undergoing re-assessment, contact laboratory |