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Variants search result for All species
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41 records found for search term Katna1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405802013CV3272000single nucleotide variantNM_007044.4(KATNA1):c.27T>A (p.Asn9Lys)not specified [RCV004403698]uncertain significance6149638521149638521Humanname
156240658CV2350358single nucleotide variantNM_007044.4(KATNA1):c.41G>A (p.Arg14His)not specified [RCV004202303]uncertain significance6149638507149638507Humanname
401758975CV2705297single nucleotide variantNM_007044.4(KATNA1):c.71C>T (p.Ser24Phe)not specified [RCV004311985]uncertain significance6149638477149638477Humanname
401779467CV2718567single nucleotide variantNM_007044.4(KATNA1):c.65A>G (p.Tyr22Cys)not specified [RCV004318366]uncertain significance6149638483149638483Humanname
597786611CV3690868single nucleotide variantNM_007044.4(KATNA1):c.40C>T (p.Arg14Cys)not specified [RCV004932298]uncertain significance6149638508149638508Humanname
598234212CV3980003single nucleotide variantNM_007044.4(KATNA1):c.29T>C (p.Val10Ala)not specified [RCV005363479]uncertain significance6149638519149638519Humanname
156335216CV2333496single nucleotide variantNM_007044.4(KATNA1):c.254C>T (p.Ala85Val)not specified [RCV004190191]uncertain significance6149632825149632825Humanname
329371030CV2461923single nucleotide variantNM_007044.4(KATNA1):c.253G>C (p.Ala85Pro)not specified [RCV004271828]uncertain significance6149632826149632826Humanname
405802017CV3272002single nucleotide variantNM_007044.4(KATNA1):c.286G>A (p.Glu96Lys)not specified [RCV004403700]uncertain significance6149632793149632793Humanname
156401239CV2210740single nucleotide variantNM_007044.4(KATNA1):c.383A>G (p.Asn128Ser)not specified [RCV004085838]uncertain significance6149623221149623221Humanname
156298384CV2251946single nucleotide variantNM_007044.4(KATNA1):c.436A>G (p.Asn146Asp)not specified [RCV004119912]uncertain significance6149623168149623168Humanname
156066295CV2349008single nucleotide variantNM_007044.4(KATNA1):c.791C>T (p.Thr264Ile)not specified [RCV004203434]uncertain significance6149601691149601691Humanname
156097307CV2399184single nucleotide variantNM_007044.4(KATNA1):c.872G>A (p.Arg291His)not specified [RCV004246614]uncertain significance6149601610149601610Humanname
329355447CV2445437single nucleotide variantNM_007044.4(KATNA1):c.319A>G (p.Arg107Gly)not specified [RCV004257499]uncertain significance6149632760149632760Humanname
401742646CV2715283single nucleotide variantNM_007044.4(KATNA1):c.550A>G (p.Ser184Gly)not specified [RCV004324622]uncertain significance6149604734149604734Humanname
401767464CV2727172single nucleotide variantNM_007044.4(KATNA1):c.655A>C (p.Lys219Gln)not specified [RCV004325526]uncertain significance6149603342149603342Humanname
401893351CV2756620single nucleotide variantNM_007044.4(KATNA1):c.515C>T (p.Ala172Val)not specified [RCV004345141]uncertain significance6149604769149604769Humanname
405802019CV3272003single nucleotide variantNM_007044.4(KATNA1):c.388C>T (p.Pro130Ser)not specified [RCV004403701]uncertain significance6149623216149623216Humanname
405802022CV3272004single nucleotide variantNM_007044.4(KATNA1):c.649G>C (p.Ala217Pro)not specified [RCV004403702]uncertain significance6149603348149603348Humanname
405802026CV3272006single nucleotide variantNM_007044.4(KATNA1):c.708G>T (p.Lys236Asn)not specified [RCV004403704]uncertain significance6149603289149603289Humanname
405802028CV3272007single nucleotide variantNM_007044.4(KATNA1):c.745G>A (p.Gly249Ser)not specified [RCV004403705]uncertain significance6149601737149601737Humanname
405802030CV3272008single nucleotide variantNM_007044.4(KATNA1):c.890C>G (p.Ala297Gly)not specified [RCV004403706]uncertain significance6149598349149598349Humanname
407467625CV3448330single nucleotide variantNM_007044.4(KATNA1):c.386G>A (p.Arg129His)not specified [RCV004635948]uncertain significance6149623218149623218Humanname
407467628CV3448331single nucleotide variantNM_007044.4(KATNA1):c.457C>T (p.Arg153Cys)not specified [RCV004635949]uncertain significance6149623147149623147Humanname
597786600CV3690865single nucleotide variantNM_007044.4(KATNA1):c.458G>A (p.Arg153His)not specified [RCV004932295]uncertain significance6149623146149623146Humanname
597786604CV3690866single nucleotide variantNM_007044.4(KATNA1):c.343C>T (p.Arg115Cys)not specified [RCV004932296]uncertain significance6149623261149623261Humanname
597786614CV3690869single nucleotide variantNM_007044.4(KATNA1):c.673G>A (p.Val225Ile)not specified [RCV004932299]uncertain significance6149603324149603324Humanname
598259139CV3980002single nucleotide variantNM_007044.4(KATNA1):c.404G>C (p.Arg135Thr)not specified [RCV005347356]uncertain significance6149623200149623200Humanname
8631872CV87078single nucleotide variantNM_007044.3(KATNA1):c.722C>T (p.Pro241Leu)Malignant melanoma [RCV000067169]not provided6149603275149603275Humanname
8631873CV87079single nucleotide variantNM_007044.3(KATNA1):c.721C>T (p.Pro241Ser)Malignant melanoma [RCV000067170]not provided6149603276149603276Humanname
156049966CV2304545single nucleotide variantNM_007044.4(KATNA1):c.1131C>G (p.Ile377Met)not specified [RCV004164623]uncertain significance6149597526149597526Humanname
156056248CV2320599single nucleotide variantNM_007044.4(KATNA1):c.1458T>G (p.Phe486Leu)not specified [RCV004172219]uncertain significance6149595054149595054Humanname
405802009CV3271998single nucleotide variantNM_007044.4(KATNA1):c.1177A>G (p.Ile393Val)not specified [RCV004403696]uncertain significance6149597163149597163Humanname
405802011CV3271999single nucleotide variantNM_007044.4(KATNA1):c.1217T>C (p.Leu406Pro)not specified [RCV004403697]uncertain significance6149597123149597123Humanname
407467622CV3448329single nucleotide variantNM_007044.4(KATNA1):c.1283C>G (p.Ala428Gly)not specified [RCV004635947]uncertain significance6149595229149595229Humanname
597786618CV3690870single nucleotide variantNM_007044.4(KATNA1):c.1448A>G (p.Lys483Arg)not specified [RCV004932300]uncertain significance6149595064149595064Humanname
598234220CV3980004single nucleotide variantNM_007044.4(KATNA1):c.1091A>C (p.Asp364Ala)not specified [RCV005363480]uncertain significance6149597566149597566Humanname
598259143CV3980005single nucleotide variantNM_007044.4(KATNA1):c.1337G>A (p.Arg446Gln)not specified [RCV005347357]uncertain significance6149595175149595175Humanname
598234226CV3980006single nucleotide variantNM_007044.4(KATNA1):c.1216C>T (p.Leu406Phe)not specified [RCV005363481]uncertain significance6149597124149597124Humanname
598234232CV3980007single nucleotide variantNM_007044.4(KATNA1):c.1175G>A (p.Arg392Gln)not specified [RCV005363482]uncertain significance6149597165149597165Humanname
598234238CV3980008single nucleotide variantNM_007044.4(KATNA1):c.1173A>C (p.Leu391Phe)not specified [RCV005363483]uncertain significance6149597167149597167Humanname