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Variants search result for Homo sapiens
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13 records found for search term Rwdd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407514136CV3473226single nucleotide variantNM_015952.4(RWDD1):c.7G>T (p.Asp3Tyr)not specified [RCV004674387]uncertain significance6116571589116571589Humanname
597733788CV3597649single nucleotide variantNM_015952.4(RWDD1):c.65C>G (p.Ser22Cys)not specified [RCV004863364]uncertain significance6116571647116571647Humanname
329354607CV2444546single nucleotide variantNM_015952.4(RWDD1):c.113C>T (p.Thr38Met)not specified [RCV004256773]uncertain significance6116580334116580334Humanname
401741550CV2713673single nucleotide variantNM_015952.4(RWDD1):c.263C>G (p.Ala88Gly)not specified [RCV004321036]uncertain significance6116584850116584850Humanname
401779959CV2725794single nucleotide variantNM_015952.4(RWDD1):c.291G>A (p.Met97Ile)not specified [RCV004316269]uncertain significance6116588862116588862Humanname
405701256CV3310012single nucleotide variantNM_015952.4(RWDD1):c.252A>T (p.Leu84Phe)not specified [RCV004447090]uncertain significance6116584839116584839Humanname
407468711CV3473225single nucleotide variantNM_015952.4(RWDD1):c.269A>T (p.Gln90Leu)not specified [RCV004661209]uncertain significance6116584856116584856Humanname
155932680CV2228708single nucleotide variantNM_015952.4(RWDD1):c.691G>A (p.Asp231Asn)not specified [RCV004093189]uncertain significance6116593060116593060Humanname
156171140CV2337487single nucleotide variantNM_015952.4(RWDD1):c.526G>A (p.Ala176Thr)not specified [RCV004187922]uncertain significance6116590383116590383Humanname
156254340CV2366449single nucleotide variantNM_015952.4(RWDD1):c.351G>C (p.Gln117His)not specified [RCV004212492]uncertain significance6116588922116588922Humanname
405700938CV3310013single nucleotide variantNM_015952.4(RWDD1):c.660C>G (p.Asp220Glu)not specified [RCV004447091]uncertain significance6116593029116593029Humanname
598233964CV3910097single nucleotide variantNM_015952.4(RWDD1):c.616A>C (p.Asn206His)not specified [RCV005274961]uncertain significance6116592985116592985Humanname
598233969CV3910098single nucleotide variantNM_015952.4(RWDD1):c.404A>C (p.Glu135Ala)not specified [RCV005274962]uncertain significance6116588975116588975Humanname