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Variants search result for Homo sapiens
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12 records found for search term Rnase4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156193777CV2350606single nucleotide variantNM_002937.5(RNASE4):c.206G>A (p.Arg69His)not specified [RCV004204951]uncertain significance142069957720699577Humanname
329360421CV2458731single nucleotide variantNM_002937.5(RNASE4):c.244C>G (p.Arg82Gly)not specified [RCV004268383]uncertain significance142069961520699615Humanname
405753842CV3316312single nucleotide variantNM_002937.5(RNASE4):c.104G>C (p.Arg35Pro)not specified [RCV004454197]uncertain significance142069947520699475Humanname
597685963CV3593873single nucleotide variantNM_002937.5(RNASE4):c.113G>A (p.Arg38Gln)not specified [RCV004858331]uncertain significance142069948420699484Humanname
598230290CV3899329single nucleotide variantNM_002937.5(RNASE4):c.167T>C (p.Met56Thr)not specified [RCV005274321]uncertain significance142069953820699538Humanname
401877994CV2760117single nucleotide variantNM_002937.5(RNASE4):c.389G>A (p.Arg130His)not specified [RCV004345521]uncertain significance142069976020699760Humanname
405753850CV3316313single nucleotide variantNM_002937.5(RNASE4):c.330G>T (p.Arg110Ser)not specified [RCV004454198]uncertain significance142069970120699701Humanname
405753858CV3316314single nucleotide variantNM_002937.5(RNASE4):c.334A>G (p.Thr112Ala)not specified [RCV004454199]uncertain significance142069970520699705Humanname
405753864CV3316315single nucleotide variantNM_002937.5(RNASE4):c.431A>G (p.His144Arg)not specified [RCV004454200]uncertain significance142069980220699802Humanname
407475936CV3483432single nucleotide variantNM_002937.5(RNASE4):c.391G>A (p.Val131Ile)not specified [RCV004663351]uncertain significance142069976220699762Humanname
598230275CV3899327single nucleotide variantNM_002937.5(RNASE4):c.388C>T (p.Arg130Cys)not specified [RCV005274319]uncertain significance142069975920699759Humanname
598230284CV3899328single nucleotide variantNM_002937.5(RNASE4):c.311T>G (p.Val104Gly)not specified [RCV005274320]uncertain significance142069968220699682Humanname