ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.1617C>A (p.Cys539Ter)

dbSNP: rs1555334436
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000647039 SCV000768826 uncertain significance Hypertrophic cardiomyopathy 14 2017-10-27 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Cys539*) in the MYH6 gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with MYH6-related disease. The current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in MYH6 cause 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.

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