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7 records found for search term Spryd4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155974146CV2235649single nucleotide variantNM_207344.4(SPRYD4):c.106G>A (p.Glu36Lys)not specified [RCV004111794]uncertain significance125646905956469059Humanname
597679770CV3604011single nucleotide variantNM_207344.4(SPRYD4):c.190G>A (p.Val64Met)not specified [RCV004857318]uncertain significance125646914356469143Humanname
598272619CV3915638single nucleotide variantNM_207344.4(SPRYD4):c.158A>T (p.Lys53Ile)not specified [RCV005282670]uncertain significance125646911156469111Humanname
598272625CV3915639single nucleotide variantNM_207344.4(SPRYD4):c.188A>G (p.Lys63Arg)not specified [RCV005282671]uncertain significance125646914156469141Humanname
598272629CV3915640single nucleotide variantNM_207344.4(SPRYD4):c.244G>T (p.Ala82Ser)not specified [RCV005282672]uncertain significance125646919756469197Humanname
329385917CV2428141single nucleotide variantNM_207344.4(SPRYD4):c.359G>A (p.Arg120His)not specified [RCV004251183]uncertain significance125646931256469312Humanname
405739520CV3333908single nucleotide variantNM_207344.4(SPRYD4):c.512C>T (p.Ser171Phe)not specified [RCV004465308]uncertain significance125646946556469465Humanname