ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.670G>A (p.Glu224Lys)

gnomAD frequency: 0.00001  dbSNP: rs727504958
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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 RCV000156363 SCV000206081 uncertain significance not specified 2014-02-11 criteria provided, single submitter clinical testing The Glu224Lys variant in GPR98 has not been previously reported in individuals w ith hearing loss or in large population studies. This variant is located in the last three bases of the exon, which is part of the 3? splice region. Computation al tools do not suggest an impact to splicing. However, this information is not predictive enough to rule out pathogenicity. Computational prediction tools and conservation analyses do not provide strong support for or against an impact of the amino acid change to the protein. In summary, additional information is need ed to fully assess the clinical significance of this variant.

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