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11 records found for search term Scrg1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156184365CV2222497single nucleotide variantNM_007281.4(SCRG1):c.49G>A (p.Gly17Arg)not specified [RCV004099342]uncertain significance4173391366173391366Humanname
329399347CV2446821single nucleotide variantNM_007281.4(SCRG1):c.29T>C (p.Ile10Thr)not specified [RCV004257676]uncertain significance4173391386173391386Humanname
401741942CV2676560single nucleotide variantNM_007281.4(SCRG1):c.52G>T (p.Val18Phe)not specified [RCV004288747]uncertain significance4173391363173391363Humanname
407461794CV3480209single nucleotide variantNM_007281.4(SCRG1):c.89G>A (p.Arg30Lys)not specified [RCV004658842]uncertain significance4173391326173391326Humanname
401762332CV2723402single nucleotide variantNM_007281.4(SCRG1):c.247G>A (p.Val83Ile)not specified [RCV004329607]likely benign4173388391173388391Humanname
405759391CV3314016single nucleotide variantNM_007281.4(SCRG1):c.124C>T (p.Pro42Ser)not specified [RCV004455031]uncertain significance4173391291173391291Humanname
405759397CV3314017single nucleotide variantNM_007281.4(SCRG1):c.287A>G (p.Asn96Ser)not specified [RCV004455032]uncertain significance4173388351173388351Humanname
405759403CV3314018single nucleotide variantNM_007281.4(SCRG1):c.291T>G (p.Asn97Lys)not specified [RCV004455033]uncertain significance4173388347173388347Humanname
597692664CV3598325single nucleotide variantNM_007281.4(SCRG1):c.127G>C (p.Glu43Gln)not specified [RCV004859032]uncertain significance4173391288173391288Humanname
598235453CV3910561single nucleotide variantNM_007281.4(SCRG1):c.223G>A (p.Glu75Lys)not specified [RCV005275249]uncertain significance4173391192173391192Humanname
598235459CV3910562single nucleotide variantNM_007281.4(SCRG1):c.289A>C (p.Asn97His)not specified [RCV005275250]uncertain significance4173388349173388349Humanname