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Variants search result for Homo sapiens
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37 records found for search term Sccpdh
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401876435CV2770860single nucleotide variantNM_016002.3(SCCPDH):c.85C>T (p.Arg29Trp)not specified [RCV004343538]uncertain significance1246724507246724507Humanname
597690389CV3601729single nucleotide variantNM_016002.3(SCCPDH):c.37T>G (p.Phe13Val)not specified [RCV004858810]uncertain significance1246724459246724459Humanname
405743436CV3317216single nucleotide variantNM_016002.3(SCCPDH):c.122C>T (p.Pro41Leu)not specified [RCV004452737]uncertain significance1246724544246724544Humanname
405743449CV3317218single nucleotide variantNM_016002.3(SCCPDH):c.295G>A (p.Val99Ile)not specified [RCV004452739]uncertain significance1246726996246726996Humanname
407461300CV3479962single nucleotide variantNM_016002.3(SCCPDH):c.269A>G (p.Lys90Arg)not specified [RCV004658677]uncertain significance1246726970246726970Humanname
597690398CV3601730single nucleotide variantNM_016002.3(SCCPDH):c.145C>T (p.Arg49Trp)not specified [RCV004858811]uncertain significance1246724567246724567Humanname
598196427CV3900326single nucleotide variantNM_016002.3(SCCPDH):c.265G>A (p.Ala89Thr)not specified [RCV005267947]uncertain significance1246726966246726966Humanname
155963625CV2197967single nucleotide variantNM_016002.3(SCCPDH):c.434G>A (p.Gly145Glu)not specified [RCV004077178]uncertain significance1246740221246740221Humanname
155960305CV2252770single nucleotide variantNM_016002.3(SCCPDH):c.714T>G (p.Cys238Trp)not specified [RCV004118612]uncertain significance1246759052246759052Humanname
156039402CV2279022single nucleotide variantNM_016002.3(SCCPDH):c.973G>A (p.Gly325Ser)not specified [RCV004145707]uncertain significance1246760210246760210Humanname
156072401CV2328776single nucleotide variantNM_016002.3(SCCPDH):c.603T>G (p.Ile201Met)not specified [RCV004178001]uncertain significance1246758264246758264Humanname
156186804CV2346639single nucleotide variantNM_016002.3(SCCPDH):c.941G>C (p.Trp314Ser)not specified [RCV004199666]uncertain significance1246760178246760178Humanname
156116976CV2349428single nucleotide variantNM_016002.3(SCCPDH):c.308G>A (p.Arg103Gln)not specified [RCV004199355]uncertain significance1246735979246735979Humanname
401735507CV2702793single nucleotide variantNM_016002.3(SCCPDH):c.496A>G (p.Thr166Ala)not specified [RCV004319360]uncertain significance1246740283246740283Humanname
401740275CV2705952single nucleotide variantNM_016002.3(SCCPDH):c.583G>A (p.Gly195Ser)not specified [RCV004320874]uncertain significance1246758244246758244Humanname
401777164CV2707771single nucleotide variantNM_016002.3(SCCPDH):c.467C>T (p.Ser156Phe)not specified [RCV004307020]uncertain significance1246740254246740254Humanname
401770262CV2711030single nucleotide variantNM_016002.3(SCCPDH):c.333A>T (p.Lys111Asn)not specified [RCV004310729]uncertain significance1246736004246736004Humanname
405743458CV3317219single nucleotide variantNM_016002.3(SCCPDH):c.605A>G (p.Tyr202Cys)not specified [RCV004452740]uncertain significance1246758266246758266Humanname
405743465CV3317220single nucleotide variantNM_016002.3(SCCPDH):c.670C>T (p.Leu224Phe)not specified [RCV004452741]uncertain significance1246758331246758331Humanname
405743470CV3317221single nucleotide variantNM_016002.3(SCCPDH):c.677G>T (p.Gly226Val)not specified [RCV004452742]uncertain significance1246758338246758338Humanname
405743478CV3317222single nucleotide variantNM_016002.3(SCCPDH):c.860T>C (p.Ile287Thr)not specified [RCV004452743]uncertain significance1246760003246760003Humanname
405743484CV3317223single nucleotide variantNM_016002.3(SCCPDH):c.907G>A (p.Gly303Arg)not specified [RCV004452744]uncertain significance1246760050246760050Humanname
405743491CV3317224single nucleotide variantNM_016002.3(SCCPDH):c.980C>G (p.Thr327Arg)not specified [RCV004452745]uncertain significance1246760217246760217Humanname
407461305CV3479963single nucleotide variantNM_016002.3(SCCPDH):c.653A>G (p.Asn218Ser)not specified [RCV004658678]uncertain significance1246758314246758314Humanname
407461312CV3479967single nucleotide variantNM_016002.3(SCCPDH):c.626A>C (p.Asn209Thr)not specified [RCV004658680]uncertain significance1246758287246758287Humanname
597690411CV3601731single nucleotide variantNM_016002.3(SCCPDH):c.942G>T (p.Trp314Cys)not specified [RCV004858812]uncertain significance1246760179246760179Humanname
597690423CV3601732single nucleotide variantNM_016002.3(SCCPDH):c.605A>T (p.Tyr202Phe)not specified [RCV004858813]uncertain significance1246758266246758266Humanname
598196420CV3900325single nucleotide variantNM_016002.3(SCCPDH):c.715C>T (p.Arg239Trp)not specified [RCV005267946]uncertain significance1246759053246759053Humanname
598196434CV3900327single nucleotide variantNM_016002.3(SCCPDH):c.617A>G (p.Asp206Gly)not specified [RCV005267948]uncertain significance1246758278246758278Humanname
598196441CV3900328single nucleotide variantNM_016002.3(SCCPDH):c.301C>T (p.Pro101Ser)not specified [RCV005267949]uncertain significance1246727002246727002Humanname
598196448CV3910271single nucleotide variantNM_016002.3(SCCPDH):c.826G>A (p.Ala276Thr)not specified [RCV005267950]uncertain significance1246759969246759969Humanname
598196453CV3910272single nucleotide variantNM_016002.3(SCCPDH):c.361A>G (p.Ile121Val)not specified [RCV005267951]uncertain significance1246736032246736032Humanname
598196464CV3910274single nucleotide variantNM_016002.3(SCCPDH):c.974G>A (p.Gly325Asp)not specified [RCV005267953]uncertain significance1246760211246760211Humanname
405743447CV3317217single nucleotide variantNM_016002.3(SCCPDH):c.1266T>A (p.Ser422Arg)not specified [RCV004452738]uncertain significance1246767276246767276Humanname
407461296CV3479961single nucleotide variantNM_016002.3(SCCPDH):c.1135G>A (p.Val379Ile)not specified [RCV004658676]uncertain significance1246766090246766090Humanname
407514435CV3479964single nucleotide variantNM_016002.3(SCCPDH):c.1048G>C (p.Gly350Arg)not specified [RCV004674547]uncertain significance1246764303246764303Humanname
407514437CV3479966single nucleotide variantNM_016002.3(SCCPDH):c.1049G>T (p.Gly350Val)not specified [RCV004674548]uncertain significance1246764304246764304Humanname