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9 records found for search term Spsb1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405738872CV3333912single nucleotide variantNM_025106.4(SPSB1):c.252G>A (p.Thr84=)not specified [RCV004465312]likely benign193561439356143Humanname
156236508CV2239020single nucleotide variantNM_025106.4(SPSB1):c.59G>A (p.Arg20Lys)not specified [RCV004109902]uncertain significance193559509355950Humanname
156086010CV2249373single nucleotide variantNM_025106.4(SPSB1):c.284G>A (p.Arg95His)not specified [RCV004118385]uncertain significance193561759356175Humanname
598272645CV3915644single nucleotide variantNM_025106.4(SPSB1):c.143A>G (p.Tyr48Cys)not specified [RCV005282676]uncertain significance193560349356034Humanname
405738646CV3333913single nucleotide variantNM_025106.4(SPSB1):c.533T>A (p.Leu178Gln)not specified [RCV004465313]uncertain significance193564249356424Humanname
405738476CV3333914single nucleotide variantNM_025106.4(SPSB1):c.697G>A (p.Glu233Lys)not specified [RCV004465314]uncertain significance193674509367450Humanname
407525749CV3478029single nucleotide variantNM_025106.4(SPSB1):c.776C>T (p.Thr259Met)not specified [RCV004679409]uncertain significance193675299367529Humanname
597778144CV3604014single nucleotide variantNM_025106.4(SPSB1):c.673C>T (p.Arg225Cys)not specified [RCV004873209]uncertain significance193565649356564Humanname
598272650CV3915645single nucleotide variantNM_025106.4(SPSB1):c.763G>T (p.Gly255Trp)not specified [RCV005282677]uncertain significance193675169367516Humanname