ClinVar Miner

Submissions for variant NM_001378609.3(OTOGL):c.6355C>T (p.Gln2119Ter)

dbSNP: rs1343148883
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
3billion RCV002052125 SCV002318598 pathogenic Autosomal recessive nonsyndromic hearing loss 84B 2022-03-22 criteria provided, single submitter clinical testing Stop-gained (nonsense): predicted to result in a loss or disruption of normal protein function through nonsense-mediated decay (NMD) or protein truncation. Multiple pathogenic variants are reported downstream of the variant.It is not observed in the gnomAD v2.1.1 dataset. This variant has been reported to be associated with OTOGL related disorder (PMID:25719458). Therefore, this variant is classified as pathogenic according to the recommendation of ACMG/AMP guideline.

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