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Pathways
Variants search result for All species
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1 records found for search term Tomt
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
14693483CV620419single nucleotide variantNM_001393500.2(TOMT):c.73C>T (p.Arg25Ter)Autosomal recessive nonsyndromic hearing loss 63 [RCV000779080]likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance117210602472106024Human1name