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9 records found for search term Tex12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597750641CV3619653single nucleotide variantNM_031275.4(TEX12):c.8C>T (p.Ala3Val)not specified [RCV004866750]uncertain significance11112169276112169276Humanname
405782113CV3342463single nucleotide variantNM_031275.4(TEX12):c.94T>A (p.Ser32Thr)not specified [RCV004472139]uncertain significance11112170449112170449Humanname
156331913CV2218232single nucleotide variantNM_031275.4(TEX12):c.286G>A (p.Ala96Thr)not specified [RCV004088432]uncertain significance11112171830112171830Humanname
156071469CV2251416single nucleotide variantNM_031275.4(TEX12):c.139T>C (p.Phe47Leu)not specified [RCV004117398]uncertain significance11112170494112170494Humanname
401863873CV2773540single nucleotide variantNM_031275.4(TEX12):c.110A>G (p.Asp37Gly)not specified [RCV004355950]uncertain significance11112170465112170465Humanname
597750627CV3619650single nucleotide variantNM_031275.4(TEX12):c.266T>C (p.Ile89Thr)not specified [RCV004866747]uncertain significance11112171810112171810Humanname
597750631CV3619651single nucleotide variantNM_031275.4(TEX12):c.127A>G (p.Ile43Val)not specified [RCV004866748]uncertain significance11112170482112170482Humanname
597750637CV3619652single nucleotide variantNM_031275.4(TEX12):c.265A>G (p.Ile89Val)not specified [RCV004866749]uncertain significance11112171809112171809Humanname
401752598CV2723289single nucleotide variantNM_031275.4(TEX12):c.310A>G (p.Ile104Val)not specified [RCV004329513]uncertain significance11112171854112171854Humanname