Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000816177 | SCV000956672 | uncertain significance | Hypertrophic cardiomyopathy | 2022-11-08 | 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. ClinVar contains an entry for this variant (Variation ID: 659211). This premature translational stop signal has been observed in individual(s) with dilated cardiomyopathy (PMID: 26383716, 32880476). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Phe735Valfs*3) in the MYH7 gene. It is expected to result in an absent or disrupted protein product. However, the current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in MYH7 cause disease. |