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Variants search result for Homo sapiens
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17 records found for search term Usf1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8598964CV27333single nucleotide variantNM_007122.5(USF1):c.*187C>THyperlipidemia, familial combined, susceptibility to [RCV000013088]risk factor1161039733161039733Human1name
401896126CV2773608single nucleotide variantNM_007122.5(USF1):c.714+3C>Tnot specified [RCV004356303]uncertain significance1161040573161040573Humanname
8598965CV27334single nucleotide variantNM_007122.5(USF1):c.561-100G>AHyperlipidemia, familial combined, susceptibility to [RCV000013089]risk factor1161040972161040972Human1name
597723001CV3629412single nucleotide variantNM_007122.5(USF1):c.29C>T (p.Thr10Met)not specified [RCV004887985]uncertain significance1161042862161042862Humanname
405810810CV3345431single nucleotide variantNM_007122.5(USF1):c.238G>A (p.Ala80Thr)not specified [RCV004482391]uncertain significance1161042154161042154Humanname
405810759CV3345432single nucleotide variantNM_007122.5(USF1):c.278C>T (p.Ala93Val)not specified [RCV004482392]uncertain significance1161041845161041845Humanname
598192161CV3936350single nucleotide variantNM_007122.5(USF1):c.269T>C (p.Met90Thr)not specified [RCV005288477]uncertain significance1161042123161042123Humanname
598192166CV3936351single nucleotide variantNM_007122.5(USF1):c.138C>A (p.Asn46Lys)not specified [RCV005288478]uncertain significance1161042591161042591Humanname
155965794CV2284067single nucleotide variantNM_007122.5(USF1):c.794T>C (p.Leu265Pro)not specified [RCV004144670]uncertain significance1161040251161040251Humanname
156353166CV2324114single nucleotide variantNM_007122.5(USF1):c.925A>G (p.Ser309Gly)not specified [RCV004178401]uncertain significance1161039928161039928Humanname
329389538CV2445215single nucleotide variantNM_007122.5(USF1):c.816G>C (p.Gln272His)not specified [RCV004263849]uncertain significance1161040229161040229Humanname
405810715CV3345433single nucleotide variantNM_007122.5(USF1):c.532A>G (p.Ile178Val)not specified [RCV004482393]uncertain significance1161041352161041352Humanname
405810681CV3345434single nucleotide variantNM_007122.5(USF1):c.836G>T (p.Arg279Leu)not specified [RCV004482394]uncertain significance1161040209161040209Humanname
407455041CV3489540single nucleotide variantNM_007122.5(USF1):c.577C>T (p.Arg193Trp)not specified [RCV004685369]uncertain significance1161040856161040856Humanname
597791303CV3629413single nucleotide variantNM_007122.5(USF1):c.574C>A (p.Pro192Thr)not specified [RCV004876616]uncertain significance1161040859161040859Humanname
597722985CV3629414single nucleotide variantNM_007122.5(USF1):c.455C>T (p.Ala152Val)not specified [RCV004887986]uncertain significance1161041668161041668Humanname
597791306CV3629415single nucleotide variantNM_007122.5(USF1):c.532A>T (p.Ile178Phe)not specified [RCV004876617]uncertain significance1161041352161041352Humanname