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Variants search result for Homo sapiens
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18 records found for search term Thoc7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407520147CV3478964single nucleotide variantNM_025075.4(THOC7):c.18C>A (p.Asp6Glu)not specified [RCV004676856]uncertain significance36386377363863773Humanname
156313552CV2196516single nucleotide variantNM_025075.4(THOC7):c.197A>G (p.Lys66Arg)not specified [RCV004073806]uncertain significance36383844063838440Humanname
156112565CV2267506single nucleotide variantNM_025075.4(THOC7):c.146A>C (p.Gln49Pro)not specified [RCV004135929]uncertain significance36383849163838491Humanname
156245582CV2267507single nucleotide variantNM_025075.4(THOC7):c.147G>T (p.Gln49His)not specified [RCV004135930]uncertain significance36383849063838490Humanname
156068134CV2320369single nucleotide variantNM_025075.4(THOC7):c.283G>A (p.Ala95Thr)not specified [RCV004178530]uncertain significance36383804563838045Humanname
155976489CV2342775single nucleotide variantNM_025075.4(THOC7):c.190A>G (p.Met64Val)not specified [RCV004189818]uncertain significance36383844763838447Humanname
401757115CV2678238single nucleotide variantNM_025075.4(THOC7):c.167C>T (p.Thr56Met)not specified [RCV004289832]uncertain significance36383847063838470Humanname
405749963CV3335531single nucleotide variantNM_025075.4(THOC7):c.103A>G (p.Ile35Val)not specified [RCV004466949]uncertain significance36383969063839690Humanname
405749968CV3335532single nucleotide variantNM_025075.4(THOC7):c.159G>A (p.Met53Ile)not specified [RCV004466950]uncertain significance36383847863838478Humanname
405749975CV3335533single nucleotide variantNM_025075.4(THOC7):c.250A>G (p.Ile84Val)not specified [RCV004466951]uncertain significance36383838763838387Humanname
156137587CV2196269single nucleotide variantNM_025075.4(THOC7):c.575A>C (p.Glu192Ala)not specified [RCV004073620]uncertain significance36383417263834172Humanname
156170952CV2267591single nucleotide variantNM_025075.4(THOC7):c.386A>C (p.His129Pro)not specified [RCV004134154]uncertain significance36383632563836325Humanname
155967381CV2280377single nucleotide variantNM_025075.4(THOC7):c.414A>C (p.Glu138Asp)not specified [RCV004140563]uncertain significance36383538763835387Humanname
156084628CV2382006single nucleotide variantNM_025075.4(THOC7):c.578C>T (p.Ala193Val)not specified [RCV004225933]uncertain significance36383416963834169Humanname
329400815CV2448928single nucleotide variantNM_025075.4(THOC7):c.456T>G (p.Ile152Met)not specified [RCV004264014]uncertain significance36383534563835345Humanname
597763233CV3613091single nucleotide variantNM_025075.4(THOC7):c.550G>A (p.Asp184Asn)not specified [RCV004869820]uncertain significance36383419763834197Humanname
597795091CV3613092single nucleotide variantNM_025075.4(THOC7):c.421G>A (p.Ala141Thr)not specified [RCV004878073]uncertain significance36383538063835380Humanname
598176144CV3913604single nucleotide variantNM_025075.4(THOC7):c.351A>C (p.Gln117His)not specified [RCV005285589]uncertain significance36383797763837977Humanname