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Variants search result for Homo sapiens
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8 records found for search term Taf11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156271238CV2195225single nucleotide variantNM_005643.4(TAF11):c.22C>A (p.Pro8Thr)not specified [RCV004080162]uncertain significance63488793634887936Humanname
405745324CV3331392single nucleotide variantNM_005643.4(TAF11):c.26C>G (p.Ser9Cys)not specified [RCV004466303]uncertain significance63488793234887932Humanname
598182018CV3919868single nucleotide variantNM_005643.4(TAF11):c.10G>A (p.Ala4Thr)not specified [RCV005286853]uncertain significance63488794834887948Humanname
597781757CV3615460single nucleotide variantNM_005643.4(TAF11):c.34G>A (p.Gly12Ser)not specified [RCV004874148]uncertain significance63488792434887924Humanname
401730090CV2700422single nucleotide variantNM_005643.4(TAF11):c.279G>T (p.Glu93Asp)not specified [RCV004311067]uncertain significance63488297334882973Humanname
156401348CV2210967single nucleotide variantNM_005643.4(TAF11):c.358C>A (p.Arg120Ser)not specified [RCV004086038]uncertain significance63488033934880339Humanname
155903779CV2298680single nucleotide variantNM_005643.4(TAF11):c.593G>C (p.Gly198Ala)not specified [RCV004156256]uncertain significance63487863334878633Humanname
401917619CV2827669single nucleotide variantNM_001401681.1(TAF11L8):c.255C>T (p.Thr85=)not provided [RCV003429580]likely benign51759070617590706Humanname