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Pathways
Variants search result for All species
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15 records found for search term Spink4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405736506CV3323252single nucleotide variantNM_014471.3(SPINK4):c.25G>A (p.Ala9Thr)not specified [RCV004465024]likely benign93324023333240233Humanname
401770791CV2707415single nucleotide variantNM_014471.3(SPINK4):c.80G>A (p.Gly27Glu)not specified [RCV004312802]uncertain significance93324513033245130Humanname
156295214CV2233712single nucleotide variantNM_014471.3(SPINK4):c.134C>A (p.Thr45Asn)not specified [RCV004100159]uncertain significance93324664733246647Humanname
156056381CV2308903single nucleotide variantNM_014471.3(SPINK4):c.229G>C (p.Asp77His)not specified [RCV004169195]uncertain significance93324843933248439Humanname
156142282CV2386034single nucleotide variantNM_014471.3(SPINK4):c.133A>G (p.Thr45Ala)not specified [RCV004229099]uncertain significance93324664633246646Humanname
156039862CV2390380single nucleotide variantNM_014471.3(SPINK4):c.185C>T (p.Thr62Met)not specified [RCV004240736]uncertain significance93324669833246698Humanname
329402844CV2451446single nucleotide variantNM_014471.3(SPINK4):c.157G>C (p.Val53Leu)not specified [RCV004272119]uncertain significance93324667033246670Humanname
401780477CV2674043single nucleotide variantNM_014471.3(SPINK4):c.212G>A (p.Arg71Gln)not specified [RCV004295455]uncertain significance93324672533246725Humanname
401878121CV2767412single nucleotide variantNM_014471.3(SPINK4):c.107T>G (p.Ile36Ser)not specified [RCV004349568]uncertain significance93324662033246620Humanname
405736467CV3323247single nucleotide variantNM_014471.3(SPINK4):c.161G>A (p.Cys54Tyr)not specified [RCV004465019]uncertain significance93324667433246674Humanname
405736474CV3323248single nucleotide variantNM_014471.3(SPINK4):c.163G>C (p.Gly55Arg)not specified [RCV004465020]uncertain significance93324667633246676Humanname
405736484CV3323249single nucleotide variantNM_014471.3(SPINK4):c.181T>C (p.Tyr61His)not specified [RCV004465021]uncertain significance93324669433246694Humanname
405736488CV3323250single nucleotide variantNM_014471.3(SPINK4):c.199C>T (p.Leu67Phe)not specified [RCV004465022]uncertain significance93324671233246712Humanname
597768623CV3607592single nucleotide variantNM_014471.3(SPINK4):c.248A>G (p.Asp83Gly)not specified [RCV004871074]uncertain significance93324845833248458Humanname
597768628CV3607593single nucleotide variantNM_014471.3(SPINK4):c.193T>C (p.Cys65Arg)not specified [RCV004871075]uncertain significance93324670633246706Humanname