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Variants search result for Homo sapiens
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24 records found for search term Ttc36
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156046717CV2268705single nucleotide variantNM_001080441.4(TTC36):c.16G>A (p.Asp6Asn)not specified [RCV004124105]uncertain significance11118527510118527510Humanname
156365145CV2272063single nucleotide variantNM_001080441.4(TTC36):c.19C>G (p.Gln7Glu)not specified [RCV004124859]uncertain significance11118527513118527513Humanname
155922846CV2217500single nucleotide variantNM_001080441.4(TTC36):c.85G>A (p.Gly29Arg)not specified [RCV004090044]uncertain significance11118527579118527579Humanname
156083937CV2381942single nucleotide variantNM_001080441.4(TTC36):c.88G>A (p.Glu30Lys)not specified [RCV004225878]uncertain significance11118527582118527582Humanname
155920976CV2212052single nucleotide variantNM_001080441.4(TTC36):c.152C>T (p.Ser51Phe)not specified [RCV004088963]uncertain significance11118528636118528636Humanname
156316116CV2250865single nucleotide variantNM_001080441.4(TTC36):c.214G>A (p.Glu72Lys)not specified [RCV004123459]uncertain significance11118528698118528698Humanname
155979908CV2336851single nucleotide variantNM_001080441.4(TTC36):c.101A>C (p.Lys34Thr)not specified [RCV004190471]uncertain significance11118527595118527595Humanname
401743223CV2687897single nucleotide variantNM_001080441.4(TTC36):c.284G>A (p.Arg95Gln)not specified [RCV004304987]uncertain significance11118528768118528768Humanname
405804352CV3337568single nucleotide variantNM_001080441.4(TTC36):c.119A>T (p.Asp40Val)not specified [RCV004479216]uncertain significance11118528603118528603Humanname
405804354CV3337569single nucleotide variantNM_001080441.4(TTC36):c.172G>C (p.Gly58Arg)not specified [RCV004479217]uncertain significance11118528656118528656Humanname
597797041CV3625454single nucleotide variantNM_001080441.4(TTC36):c.247G>A (p.Glu83Lys)not specified [RCV004878686]uncertain significance11118528731118528731Humanname
598253397CV3925285single nucleotide variantNM_001080441.4(TTC36):c.283C>T (p.Arg95Trp)not specified [RCV005299067]uncertain significance11118528767118528767Humanname
598253402CV3925287single nucleotide variantNM_001080441.4(TTC36):c.173G>C (p.Gly58Ala)not specified [RCV005299068]uncertain significance11118528657118528657Humanname
155969630CV2309093single nucleotide variantNM_001080441.4(TTC36):c.473G>A (p.Arg158Gln)not specified [RCV004171453]uncertain significance11118530819118530819Humanname
156053966CV2385696single nucleotide variantNM_001080441.4(TTC36):c.556C>T (p.Arg186Cys)not specified [RCV004233322]uncertain significance11118530902118530902Humanname
156103385CV2386901single nucleotide variantNM_001080441.4(TTC36):c.518G>T (p.Arg173Leu)not specified [RCV004233533]uncertain significance11118530864118530864Humanname
401733775CV2687830single nucleotide variantNM_001080441.4(TTC36):c.353G>T (p.Arg118Leu)not specified [RCV004303139]uncertain significance11118530699118530699Humanname
405804356CV3337570single nucleotide variantNM_001080441.4(TTC36):c.311C>T (p.Ala104Val)not specified [RCV004479218]uncertain significance11118530657118530657Humanname
405804360CV3337572single nucleotide variantNM_001080441.4(TTC36):c.352C>T (p.Arg118Trp)not specified [RCV004479220]uncertain significance11118530698118530698Humanname
405804362CV3337573single nucleotide variantNM_001080441.4(TTC36):c.424G>A (p.Ala142Thr)not specified [RCV004479221]uncertain significance11118530770118530770Humanname
597797038CV3625453single nucleotide variantNM_001080441.4(TTC36):c.428G>A (p.Arg143His)not specified [RCV004878685]uncertain significance11118530774118530774Humanname
598230651CV3925286single nucleotide variantNM_001080441.4(TTC36):c.353G>C (p.Arg118Pro)not specified [RCV005295079]uncertain significance11118530699118530699Humanname
598253408CV3925288single nucleotide variantNM_001080441.4(TTC36):c.432G>T (p.Arg144Ser)not specified [RCV005299069]uncertain significance11118530778118530778Humanname
598230659CV3925290single nucleotide variantNM_001080441.4(TTC36):c.464C>T (p.Pro155Leu)not specified [RCV005295080]uncertain significance11118530810118530810Humanname