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Variants search result for Homo sapiens
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10 records found for search term Timm13
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597764472CV3613467single nucleotide variantNM_012458.4(TIMM13):c.11G>A (p.Gly4Asp)not specified [RCV004870146]uncertain significance1924275232427523Humanname
156367095CV2269822single nucleotide variantNM_012458.4(TIMM13):c.35C>T (p.Ser12Phe)not specified [RCV004127061]uncertain significance1924274992427499Humanname
401720029CV2705621single nucleotide variantNM_012458.4(TIMM13):c.56C>G (p.Pro19Arg)not specified [RCV004318481]uncertain significance1924274782427478Humanname
156360698CV2329593single nucleotide variantNM_012458.4(TIMM13):c.134A>G (p.Lys45Arg)not specified [RCV004180713]uncertain significance1924273112427311Humanname
401781611CV2682058single nucleotide variantNM_012458.4(TIMM13):c.242C>T (p.Ser81Phe)not specified [RCV004290123]uncertain significance1924269942426994Humanname
405768366CV3345887single nucleotide variantNM_012458.4(TIMM13):c.119A>G (p.Gln40Arg)not specified [RCV004469849]uncertain significance1924274152427415Humanname
407458444CV3475693single nucleotide variantNM_012458.4(TIMM13):c.235A>G (p.Thr79Ala)not specified [RCV004686821]uncertain significance1924270012427001Humanname
597764467CV3613466single nucleotide variantNM_012458.4(TIMM13):c.182C>T (p.Ser61Phe)not specified [RCV004870145]uncertain significance1924272632427263Humanname
597764475CV3613468single nucleotide variantNM_012458.4(TIMM13):c.277G>A (p.Ala93Thr)not specified [RCV004870147]uncertain significance1924269592426959Humanname
598197723CV3924243single nucleotide variantNM_012458.4(TIMM13):c.215G>A (p.Arg72His)not specified [RCV005289617]uncertain significance1924270212427021Humanname