ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.13238C>G (p.Pro4413Arg)

dbSNP: rs1553252404
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000615143 SCV000731626 uncertain significance not specified 2017-07-27 criteria provided, single submitter clinical testing Variant classified as Uncertain Significance - Favor Pathogenic. The p.Pro4413Ar g variant in USH2A has been reported by our laboratory in one individual with he aring loss, who has another variant of uncertain significance on the same copy a nd a pathogenic variant on the other copy of the USH2A gene. The p.Pro4413Arg ha s not been identified in large population studies. Computational prediction tool s and conservation analyses suggest that this variant may impact the protein, th ough this information is not predictive enough to determine pathogenicity. In su mmary, while there is some suspicion of a pathogenic role, the clinical signific ance of the p.Pro4413Arg variant is uncertain.

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