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34 records found for search term Kti12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156167651CV2345322single nucleotide variantNM_138417.3(KTI12):c.50G>A (p.Arg17His)not specified [RCV004198102]uncertain significance15203371252033712Humanname
329394084CV2450065single nucleotide variantNM_138417.3(KTI12):c.37G>T (p.Gly13Cys)not specified [RCV004269113]uncertain significance15203372552033725Humanname
597795182CV3692633single nucleotide variantNM_138417.3(KTI12):c.29C>T (p.Pro10Leu)not specified [RCV004934786]uncertain significance15203373352033733Humanname
156103168CV2260484single nucleotide variantNM_138417.3(KTI12):c.103G>A (p.Val35Met)not specified [RCV004123274]uncertain significance15203365952033659Humanname
329370401CV2435570single nucleotide variantNM_138417.3(KTI12):c.254A>G (p.Lys85Arg)not specified [RCV004254825]uncertain significance15203350852033508Humanname
405808318CV3266137single nucleotide variantNM_138417.3(KTI12):c.286C>T (p.Arg96Trp)not specified [RCV004407019]uncertain significance15203347652033476Humanname
598196689CV3991406single nucleotide variantNM_138417.3(KTI12):c.194C>T (p.Ser65Phe)not specified [RCV005355223]uncertain significance15203356852033568Humanname
598196706CV3991409single nucleotide variantNM_138417.3(KTI12):c.146A>C (p.Tyr49Ser)not specified [RCV005355225]uncertain significance15203361652033616Humanname
156291613CV2246441single nucleotide variantNM_138417.3(KTI12):c.754C>G (p.Arg252Gly)not specified [RCV004110211]uncertain significance15203300852033008Humanname
156232872CV2273817single nucleotide variantNM_138417.3(KTI12):c.497C>T (p.Ala166Val)not specified [RCV004132449]likely benign15203326552033265Humanname
156363038CV2330491single nucleotide variantNM_138417.3(KTI12):c.680G>A (p.Arg227Gln)not specified [RCV004181058]uncertain significance15203308252033082Humanname
329384566CV2435137single nucleotide variantNM_138417.3(KTI12):c.819G>T (p.Gln273His)not specified [RCV004252778]uncertain significance15203294352032943Humanname
329402654CV2451118single nucleotide variantNM_138417.3(KTI12):c.713C>T (p.Pro238Leu)not specified [RCV004270057]uncertain significance15203304952033049Humanname
401784218CV2721160single nucleotide variantNM_138417.3(KTI12):c.566C>G (p.Thr189Ser)not specified [RCV004330148]uncertain significance15203319652033196Humanname
401871015CV2788986single nucleotide variantNM_138417.3(KTI12):c.814C>T (p.His272Tyr)not specified [RCV004363300]uncertain significance15203294852032948Humanname
405808320CV3266138single nucleotide variantNM_138417.3(KTI12):c.307T>G (p.Cys103Gly)not specified [RCV004407020]uncertain significance15203345552033455Humanname
405808322CV3266139single nucleotide variantNM_138417.3(KTI12):c.326G>C (p.Arg109Pro)not specified [RCV004407021]uncertain significance15203343652033436Humanname
405808324CV3266140single nucleotide variantNM_138417.3(KTI12):c.423C>G (p.Asp141Glu)not specified [RCV004407022]uncertain significance15203333952033339Humanname
405808326CV3266141single nucleotide variantNM_138417.3(KTI12):c.454C>T (p.Leu152Phe)not specified [RCV004407023]uncertain significance15203330852033308Humanname
405808328CV3266142single nucleotide variantNM_138417.3(KTI12):c.598T>G (p.Ser200Ala)not specified [RCV004407024]uncertain significance15203316452033164Humanname
405808332CV3266144single nucleotide variantNM_138417.3(KTI12):c.844C>G (p.Leu282Val)not specified [RCV004407026]uncertain significance15203291852032918Humanname
407480975CV3455975single nucleotide variantNM_138417.3(KTI12):c.601G>A (p.Gly201Ser)not specified [RCV004639793]likely benign15203316152033161Humanname
597795179CV3692628single nucleotide variantNM_138417.3(KTI12):c.616C>A (p.Pro206Thr)not specified [RCV004934785]uncertain significance15203314652033146Humanname
597624976CV3692631single nucleotide variantNM_138417.3(KTI12):c.373A>G (p.Asn125Asp)not specified [RCV004938021]uncertain significance15203338952033389Humanname
597624977CV3692632single nucleotide variantNM_138417.3(KTI12):c.355G>A (p.Val119Met)not specified [RCV004938022]uncertain significance15203340752033407Humanname
598196675CV3991402single nucleotide variantNM_138417.3(KTI12):c.967C>T (p.Arg323Cys)not specified [RCV005355221]uncertain significance15203279552032795Humanname
598173471CV3991403single nucleotide variantNM_138417.3(KTI12):c.385A>G (p.Asn129Asp)not specified [RCV005370936]uncertain significance15203337752033377Humanname
598222451CV3991404single nucleotide variantNM_138417.3(KTI12):c.806G>A (p.Ser269Asn)not specified [RCV005360990]uncertain significance15203295652032956Humanname
598196682CV3991405single nucleotide variantNM_138417.3(KTI12):c.980C>G (p.Ser327Trp)not specified [RCV005355222]uncertain significance15203278252032782Humanname
598173478CV3991408single nucleotide variantNM_138417.3(KTI12):c.733C>T (p.Arg245Cys)not specified [RCV005370937]uncertain significance15203302952033029Humanname
156170030CV2276873single nucleotide variantNM_138417.3(KTI12):c.1052A>G (p.Gln351Arg)not specified [RCV004140216]uncertain significance15203271052032710Humanname
156180414CV2324440single nucleotide variantNM_138417.3(KTI12):c.1051C>G (p.Gln351Glu)not specified [RCV004178928]uncertain significance15203271152032711Humanname
401896410CV2781294single nucleotide variantNM_138417.3(KTI12):c.1001A>G (p.Asn334Ser)not specified [RCV004352316]uncertain significance15203276152032761Humanname
597624975CV3692629single nucleotide variantNM_138417.3(KTI12):c.1031T>C (p.Met344Thr)not specified [RCV004938020]uncertain significance15203273152032731Humanname