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Variants search result for Homo sapiens
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12 records found for search term Ttc9b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156139388CV2280743single nucleotide variantNM_152479.6(TTC9B):c.52C>A (p.Pro18Thr)not specified [RCV004143193]uncertain significance194021833040218330Humanname
156369909CV2263440single nucleotide variantNM_152479.6(TTC9B):c.269G>A (p.Arg90Gln)not specified [RCV004133686]uncertain significance194021811340218113Humanname
401748820CV2708362single nucleotide variantNM_152479.6(TTC9B):c.193G>A (p.Ala65Thr)not specified [RCV004313480]uncertain significance194021818940218189Humanname
407531885CV3487317single nucleotide variantNM_152479.6(TTC9B):c.101G>A (p.Gly34Asp)not specified [RCV004682726]uncertain significance194021828140218281Humanname
597797189CV3625553single nucleotide variantNM_152479.6(TTC9B):c.112C>T (p.Arg38Cys)not specified [RCV004878764]uncertain significance194021827040218270Humanname
156269689CV2326402single nucleotide variantNM_152479.6(TTC9B):c.469C>A (p.Arg157Ser)not specified [RCV004182976]uncertain significance194021732840217328Humanname
329369718CV2461196single nucleotide variantNM_152479.6(TTC9B):c.659G>A (p.Arg220His)not specified [RCV004267393]uncertain significance194021622440216224Humanname
401879965CV2783049single nucleotide variantNM_152479.6(TTC9B):c.592C>G (p.Arg198Gly)not specified [RCV004363419]uncertain significance194021720540217205Humanname
405804521CV3337646single nucleotide variantNM_152479.6(TTC9B):c.425C>G (p.Thr142Arg)not specified [RCV004479294]uncertain significance194021795740217957Humanname
597797183CV3625551single nucleotide variantNM_152479.6(TTC9B):c.565C>G (p.Arg189Gly)not specified [RCV004878762]uncertain significance194021723240217232Humanname
597797186CV3625552single nucleotide variantNM_152479.6(TTC9B):c.692G>A (p.Gly231Glu)not specified [RCV004878763]uncertain significance194021619140216191Humanname
598253621CV3925347single nucleotide variantNM_152479.6(TTC9B):c.607A>G (p.Thr203Ala)not specified [RCV005299105]uncertain significance194021719040217190Humanname