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Variants search result for Homo sapiens
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34 records found for search term Gtpbp10
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405719406CV3255616single nucleotide variantNM_033107.4(GTPBP10):c.8A>C (p.His3Pro)not specified [RCV004388573]uncertain significance79034674990346749Humanname
155959354CV2193864single nucleotide variantNM_033107.4(GTPBP10):c.175A>G (p.Lys59Glu)not specified [RCV004074608]uncertain significance79035295790352957Humanname
156062475CV2231994single nucleotide variantNM_033107.4(GTPBP10):c.275T>C (p.Val92Ala)not specified [RCV004093052]uncertain significance79035450590354505Humanname
156008840CV2294277single nucleotide variantNM_033107.4(GTPBP10):c.250A>G (p.Lys84Glu)not specified [RCV004151409]uncertain significance79035448090354480Humanname
329372687CV2428608single nucleotide variantNM_033107.4(GTPBP10):c.146C>T (p.Ala49Val)not specified [RCV004255414]uncertain significance79035292890352928Humanname
407464585CV3443612single nucleotide variantNM_033107.4(GTPBP10):c.190C>T (p.Arg64Trp)not specified [RCV004635115]uncertain significance79035297290352972Humanname
597771929CV3688888single nucleotide variantNM_033107.4(GTPBP10):c.191G>A (p.Arg64Gln)not specified [RCV004928573]likely benign79035297390352973Humanname
597757214CV3688891single nucleotide variantNM_033107.4(GTPBP10):c.251A>G (p.Lys84Arg)not specified [RCV004925031]uncertain significance79035448190354481Humanname
597757219CV3688892single nucleotide variantNM_033107.4(GTPBP10):c.127G>A (p.Gly43Ser)not specified [RCV004925032]uncertain significance79035290990352909Humanname
597757224CV3688893single nucleotide variantNM_033107.4(GTPBP10):c.177A>C (p.Lys59Asn)not specified [RCV004925033]uncertain significance79035295990352959Humanname
598253265CV3974887single nucleotide variantNM_033107.4(GTPBP10):c.259G>A (p.Asp87Asn)not specified [RCV005346229]uncertain significance79035448990354489Humanname
156381802CV2212380single nucleotide variantNM_033107.4(GTPBP10):c.337A>G (p.Asn113Asp)not specified [RCV004091319]uncertain significance79035510390355103Humanname
156002275CV2287983single nucleotide variantNM_033107.4(GTPBP10):c.733A>G (p.Thr245Ala)not specified [RCV004147754]uncertain significance79037816790378167Humanname
156086329CV2289939single nucleotide variantNM_033107.4(GTPBP10):c.578G>A (p.Ser193Asn)not specified [RCV004150589]likely benign79037434190374341Humanname
155929921CV2299623single nucleotide variantNM_033107.4(GTPBP10):c.920A>C (p.Glu307Ala)not specified [RCV004154943]uncertain significance79038491090384910Humanname
156080004CV2300968single nucleotide variantNM_033107.4(GTPBP10):c.877A>G (p.Met293Val)not specified [RCV004158145]uncertain significance79038305590383055Humanname
156350164CV2316153single nucleotide variantNM_033107.4(GTPBP10):c.968C>T (p.Pro323Leu)not specified [RCV004174199]uncertain significance79038495890384958Humanname
156283204CV2318821single nucleotide variantNM_033107.4(GTPBP10):c.596C>T (p.Ser199Leu)not specified [RCV004175733]uncertain significance79037751190377511Humanname
329366471CV2445760single nucleotide variantNM_033107.4(GTPBP10):c.728C>T (p.Ser243Phe)not specified [RCV004259822]uncertain significance79037816290378162Humanname
329354837CV2449106single nucleotide variantNM_033107.4(GTPBP10):c.611C>T (p.Pro204Leu)not specified [RCV004264168]uncertain significance79037752690377526Humanname
401772911CV2709019single nucleotide variantNM_033107.4(GTPBP10):c.954C>G (p.Phe318Leu)not specified [RCV004314372]uncertain significance79038494490384944Humanname
401774844CV2713665single nucleotide variantNM_033107.4(GTPBP10):c.773C>G (p.Thr258Arg)not specified [RCV004321031]uncertain significance79037820790378207Humanname
401860762CV2776180single nucleotide variantNM_033107.4(GTPBP10):c.392T>G (p.Phe131Cys)not specified [RCV004353264]uncertain significance79035515890355158Humanname
405719376CV3255613single nucleotide variantNM_033107.4(GTPBP10):c.568A>T (p.Ile190Leu)not specified [RCV004388570]uncertain significance79037433190374331Humanname
405719390CV3255614single nucleotide variantNM_033107.4(GTPBP10):c.577A>G (p.Ser193Gly)not specified [RCV004388571]uncertain significance79037434090374340Humanname
405719395CV3255615single nucleotide variantNM_033107.4(GTPBP10):c.607C>A (p.Leu203Ile)not specified [RCV004388572]uncertain significance79037752290377522Humanname
407464580CV3443611single nucleotide variantNM_033107.4(GTPBP10):c.608T>A (p.Leu203His)not specified [RCV004635114]uncertain significance79037752390377523Humanname
597771933CV3688890single nucleotide variantNM_033107.4(GTPBP10):c.847C>G (p.Pro283Ala)not specified [RCV004928574]uncertain significance79038302590383025Humanname
597757227CV3688895single nucleotide variantNM_033107.4(GTPBP10):c.980T>A (p.Val327Asp)not specified [RCV004925034]uncertain significance79038497090384970Humanname
598253259CV3974886single nucleotide variantNM_033107.4(GTPBP10):c.312A>C (p.Lys104Asn)not specified [RCV005346228]uncertain significance79035454290354542Humanname
405719369CV3255612single nucleotide variantNM_033107.4(GTPBP10):c.1045C>G (p.Gln349Glu)not specified [RCV004388569]uncertain significance79038503590385035Humanname
597757209CV3688889single nucleotide variantNM_033107.4(GTPBP10):c.1027C>G (p.Leu343Val)not specified [RCV004925030]uncertain significance79038501790385017Humanname
598235532CV3974889single nucleotide variantNM_033107.4(GTPBP10):c.1015A>G (p.Ile339Val)not specified [RCV005343067]uncertain significance79038500590385005Humanname
8632686CV87901single nucleotide variantNM_001042717.2(GTPBP10):c.730C>T (p.Pro244Ser)Malignant melanoma [RCV000067993]not provided79038495790384957Humanname