ClinVar Miner

Submissions for variant NM_206933.3(USH2A):c.12151G>T (p.Glu4051Ter) (rs1262416703)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneID Lab - Advanced Molecular Diagnostics RCV000680443 SCV000807816 likely pathogenic Usher syndrome, type 2A 2018-03-10 criteria provided, single submitter clinical testing This variant creates a premature stop codon at position 4051 of the protein that could potentially result in a defective USH2A protein due to protein truncation or nonsense-mediated mRNA decay. This mutation is considered a non-tolerated amino acid change based on in silico prediction algorithms (disease causing), and it has not been reported in the ClinVar Database (NCBI National Library of Medicine, NIH, Bethesda MD), or in population databases such as ExAC or 1000 genomes. Based on these findings and the limited literature regarding this substitution we consider it as a likely pathogenic variant.

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