ClinVar Miner

Submissions for variant NM_001378609.3(OTOGL):c.5350G>A (p.Val1784Met)

gnomAD frequency: 0.00015  dbSNP: rs571909899
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001950177 SCV002206881 uncertain significance not provided 2022-10-17 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 1429797). This variant has not been reported in the literature in individuals affected with OTOGL-related conditions. This variant is present in population databases (rs571909899, gnomAD 0.1%). This sequence change replaces valine, which is neutral and non-polar, with methionine, which is neutral and non-polar, at codon 1775 of the OTOGL protein (p.Val1775Met).
Revvity Omics, Revvity RCV003134263 SCV003816550 uncertain significance Autosomal recessive nonsyndromic hearing loss 84B 2022-03-30 criteria provided, single submitter clinical testing

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