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Variants search result for Homo sapiens
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7 records found for search term Hcst
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405790195CV3266410single nucleotide variantNM_014266.4(HCST):c.20T>A (p.Ile7Asn)not specified [RCV004399420]uncertain significance193590261335902613Humanname
407514410CV3440212single nucleotide variantNM_014266.4(HCST):c.35T>C (p.Leu12Ser)not specified [RCV004627598]uncertain significance193590262835902628Humanname
597710257CV3679050single nucleotide variantNM_014266.4(HCST):c.79T>G (p.Ser27Ala)not specified [RCV004917437]uncertain significance193590338635903386Humanname
155918946CV2333101single nucleotide variantNM_014266.4(HCST):c.124T>C (p.Cys42Arg)not specified [RCV004194394]uncertain significance193590378635903786Humanname
329363465CV2471646single nucleotide variantNM_014266.4(HCST):c.125G>A (p.Cys42Tyr)not specified [RCV004286936]uncertain significance193590378735903787Humanname
597781558CV3679048single nucleotide variantNM_014266.4(HCST):c.152C>T (p.Ala51Val)not specified [RCV004930927]uncertain significance193590381435903814Humanname
597710248CV3679049single nucleotide variantNM_014266.4(HCST):c.266T>C (p.Met89Thr)not specified [RCV004917436]uncertain significance193590414435904144Humanname