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17 records found for search term Hcfc1r1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405789882CV3266326single nucleotide variantNM_017885.4(HCFC1R1):c.44C>T (p.Ala15Val)not specified [RCV004399336]uncertain significance1630238983023898Humanname
598246647CV3971565single nucleotide variantNM_017885.4(HCFC1R1):c.47A>T (p.Gln16Leu)not specified [RCV005345185]uncertain significance1630238953023895Humanname
156274852CV2279862single nucleotide variantNM_017885.4(HCFC1R1):c.179C>T (p.Ser60Phe)not specified [RCV004144456]uncertain significance1630233353023335Humanname
156224059CV2395075single nucleotide variantNM_017885.4(HCFC1R1):c.250A>G (p.Met84Val)not specified [RCV004236759]uncertain significance1630232643023264Humanname
401870196CV2765710single nucleotide variantNM_017885.4(HCFC1R1):c.103C>G (p.Leu35Val)not specified [RCV004335716]uncertain significance1630235233023523Humanname
401888311CV2788302single nucleotide variantNM_017885.4(HCFC1R1):c.118C>T (p.Pro40Ser)not specified [RCV004352887]uncertain significance1630235083023508Humanname
407504775CV3440148single nucleotide variantNM_017885.4(HCFC1R1):c.247C>A (p.Pro83Thr)not specified [RCV004624145]uncertain significance1630232673023267Humanname
407514299CV3440149single nucleotide variantNM_017885.4(HCFC1R1):c.199C>A (p.His67Asn)not specified [RCV004627541]uncertain significance1630233153023315Humanname
598266087CV3971567single nucleotide variantNM_017885.4(HCFC1R1):c.244C>T (p.Pro82Ser)not specified [RCV005349184]uncertain significance1630232703023270Humanname
156240085CV2236006single nucleotide variantNM_017885.4(HCFC1R1):c.311G>A (p.Arg104His)not specified [RCV004113876]uncertain significance1630229693022969Humanname
156130829CV2372702single nucleotide variantNM_017885.4(HCFC1R1):c.299T>C (p.Leu100Pro)not specified [RCV004221896]uncertain significance1630229813022981Humanname
401738326CV2714414single nucleotide variantNM_017885.4(HCFC1R1):c.344G>A (p.Arg115His)not specified [RCV004317947]uncertain significance1630229363022936Humanname
405789878CV3266325single nucleotide variantNM_017885.4(HCFC1R1):c.317C>T (p.Pro106Leu)not specified [RCV004399335]uncertain significance1630229633022963Humanname
407514301CV3440150single nucleotide variantNM_017885.4(HCFC1R1):c.344G>T (p.Arg115Leu)not specified [RCV004627542]uncertain significance1630229363022936Humanname
597781384CV3682342single nucleotide variantNM_017885.4(HCFC1R1):c.367C>T (p.Pro123Ser)not specified [RCV004930906]uncertain significance1630229133022913Humanname
597781388CV3682343single nucleotide variantNM_017885.4(HCFC1R1):c.412C>G (p.Leu138Val)not specified [RCV004930907]uncertain significance1630228683022868Humanname
598266082CV3971566single nucleotide variantNM_017885.4(HCFC1R1):c.338C>T (p.Ala113Val)not specified [RCV005349183]uncertain significance1630229423022942Humanname