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Variants search result for Homo sapiens
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62 records found for search term Hipk4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405779059CV3270364single nucleotide variantNM_144685.5(HIPK4):c.17C>T (p.Ser6Leu)not specified [RCV004397282]uncertain significance194038988640389886Humanname
405779065CV3270365single nucleotide variantNM_144685.5(HIPK4):c.25G>A (p.Asp9Asn)not specified [RCV004397283]uncertain significance194038987840389878Humanname
405779092CV3270370single nucleotide variantNM_144685.5(HIPK4):c.92G>A (p.Arg31Gln)not specified [RCV004397288]uncertain significance194038981140389811Humanname
407527279CV3437381single nucleotide variantNM_144685.5(HIPK4):c.43G>A (p.Glu15Lys)not specified [RCV004632739]uncertain significance194038986040389860Humanname
156174172CV2194407single nucleotide variantNM_144685.5(HIPK4):c.103G>A (p.Glu35Lys)not specified [RCV004079508]uncertain significance194038980040389800Humanname
156196195CV2241527single nucleotide variantNM_144685.5(HIPK4):c.193C>G (p.Leu65Val)not specified [RCV004104426]uncertain significance194038971040389710Humanname
156395697CV2325871single nucleotide variantNM_144685.5(HIPK4):c.152T>A (p.Ile51Asn)not specified [RCV004174055]uncertain significance194038975140389751Humanname
329385053CV2454626single nucleotide variantNM_144685.5(HIPK4):c.149G>T (p.Arg50Leu)not specified [RCV004268086]uncertain significance194038975440389754Humanname
401767134CV2681464single nucleotide variantNM_144685.5(HIPK4):c.123C>G (p.Ile41Met)not specified [RCV004292002]uncertain significance194038978040389780Humanname
405779070CV3270366single nucleotide variantNM_144685.5(HIPK4):c.286C>T (p.Leu96Phe)not specified [RCV004397284]uncertain significance194038961740389617Humanname
597790244CV3682476single nucleotide variantNM_144685.5(HIPK4):c.245C>T (p.Ala82Val)not specified [RCV004933167]uncertain significance194038965840389658Humanname
598178298CV3978918single nucleotide variantNM_144685.5(HIPK4):c.221G>A (p.Arg74His)not specified [RCV005351966]uncertain significance194038968240389682Humanname
15126202CV716449single nucleotide variantNM_144685.5(HIPK4):c.1032C>T (p.His344=)not provided [RCV000963706]benign194038095940380959Humanname
156377751CV2211427single nucleotide variantNM_144685.5(HIPK4):c.674G>A (p.Arg225His)not specified [RCV004090334]uncertain significance194038393140383931Humanname
156069714CV2232266single nucleotide variantNM_144685.5(HIPK4):c.376C>T (p.Arg126Trp)not specified [RCV004105049]uncertain significance194038952740389527Humanname
156039030CV2278988single nucleotide variantNM_144685.5(HIPK4):c.814G>A (p.Glu272Lys)not specified [RCV004145677]uncertain significance194038379140383791Humanname
156115082CV2349260single nucleotide variantNM_144685.5(HIPK4):c.922C>T (p.Arg308Trp)not specified [RCV004199207]uncertain significance194038106940381069Humanname
156132805CV2350197single nucleotide variantNM_144685.5(HIPK4):c.899C>A (p.Ala300Asp)not specified [RCV004200111]uncertain significance194038109240381092Humanname
401884083CV2765027single nucleotide variantNM_144685.5(HIPK4):c.818C>T (p.Thr273Met)not specified [RCV004337149]uncertain significance194038378740383787Humanname
405779075CV3270367single nucleotide variantNM_144685.5(HIPK4):c.490A>G (p.Ile164Val)not specified [RCV004397285]uncertain significance194038411540384115Humanname
405779080CV3270368single nucleotide variantNM_144685.5(HIPK4):c.827G>A (p.Arg276His)not specified [RCV004397286]uncertain significance194038116440381164Humanname
405779087CV3270369single nucleotide variantNM_144685.5(HIPK4):c.870G>T (p.Gln290His)not specified [RCV004397287]uncertain significance194038112140381121Humanname
407527276CV3437380single nucleotide variantNM_144685.5(HIPK4):c.725C>A (p.Ala242Asp)not specified [RCV004632738]uncertain significance194038388040383880Humanname
407527282CV3437382single nucleotide variantNM_144685.5(HIPK4):c.574T>G (p.Phe192Val)not specified [RCV004632740]uncertain significance194038403140384031Humanname
597790240CV3682475single nucleotide variantNM_144685.5(HIPK4):c.842G>A (p.Arg281His)not specified [RCV004933166]uncertain significance194038114940381149Humanname
597790256CV3682479single nucleotide variantNM_144685.5(HIPK4):c.839G>A (p.Arg280His)not specified [RCV004933170]uncertain significance194038115240381152Humanname
597790263CV3682481single nucleotide variantNM_144685.5(HIPK4):c.841C>T (p.Arg281Cys)not specified [RCV004933172]uncertain significance194038115040381150Humanname
598178264CV3978912single nucleotide variantNM_144685.5(HIPK4):c.833T>C (p.Leu278Ser)not specified [RCV005351961]uncertain significance194038115840381158Humanname
598248240CV3978915single nucleotide variantNM_144685.5(HIPK4):c.940C>T (p.His314Tyr)not specified [RCV005345414]uncertain significance194038105140381051Humanname
598178307CV3978919single nucleotide variantNM_144685.5(HIPK4):c.838C>T (p.Arg280Cys)not specified [RCV005351967]uncertain significance194038115340381153Humanname
598178313CV3978921single nucleotide variantNM_144685.5(HIPK4):c.592G>A (p.Val198Met)not specified [RCV005351968]likely benign194038401340384013Humanname
598178322CV3978923single nucleotide variantNM_144685.5(HIPK4):c.738C>A (p.His246Gln)not specified [RCV005351969]uncertain significance194038386740383867Humanname
598178335CV3978925single nucleotide variantNM_144685.5(HIPK4):c.946G>A (p.Asp316Asn)not specified [RCV005351971]uncertain significance194038104540381045Humanname
15161950CV728187single nucleotide variantNM_144685.5(HIPK4):c.911C>T (p.Thr304Ile)not provided [RCV000881666]benign194038108040381080Humanname
9687124CV171633single nucleotide variantNM_144685.5(HIPK4):c.1279G>A (p.Asp427Asn)Prostate cancer [RCV000149343]uncertain significance194038071240380712Human2name
156031332CV2202671single nucleotide variantNM_144685.5(HIPK4):c.1588G>A (p.Gly530Arg)not specified [RCV004082921]uncertain significance194038040340380403Humanname
156038159CV2214877single nucleotide variantNM_144685.5(HIPK4):c.1442G>A (p.Arg481His)not specified [RCV004084673]uncertain significance194038054940380549Humanname
156277771CV2252031single nucleotide variantNM_144685.5(HIPK4):c.1195A>G (p.Lys399Glu)not specified [RCV004122067]likely benign194038079640380796Humanname
156076748CV2291552single nucleotide variantNM_144685.5(HIPK4):c.1100G>A (p.Arg367His)not specified [RCV004155855]uncertain significance194038089140380891Humanname
156259301CV2322219single nucleotide variantNM_144685.5(HIPK4):c.1747G>A (p.Val583Ile)not specified [RCV004175992]likely benign194037969140379691Humanname
155968471CV2337847single nucleotide variantNM_144685.5(HIPK4):c.1288G>C (p.Asp430His)not specified [RCV004183857]uncertain significance194038070340380703Humanname
155983440CV2371279single nucleotide variantNM_144685.5(HIPK4):c.1225G>A (p.Gly409Ser)not specified [RCV004221012]likely benign194038076640380766Humanname
156260848CV2381237single nucleotide variantNM_144685.5(HIPK4):c.1534C>A (p.Pro512Thr)not specified [RCV004227303]uncertain significance194038045740380457Humanname
156000284CV2383189single nucleotide variantNM_144685.5(HIPK4):c.1042T>A (p.Ser348Thr)not specified [RCV004220201]uncertain significance194038094940380949Humanname
401730823CV2677356single nucleotide variantNM_144685.5(HIPK4):c.1069G>A (p.Glu357Lys)not specified [RCV004289064]uncertain significance194038092240380922Humanname
401868835CV2767357single nucleotide variantNM_144685.5(HIPK4):c.1343A>G (p.Asn448Ser)not specified [RCV004349518]uncertain significance194038064840380648Humanname
401879369CV2773050single nucleotide variantNM_144685.5(HIPK4):c.1607T>G (p.Leu536Arg)not specified [RCV004351490]uncertain significance194038038440380384Humanname
401898443CV2787917single nucleotide variantNM_144685.5(HIPK4):c.1657A>G (p.Met553Val)not specified [RCV004358589]uncertain significance194038033440380334Humanname
405779047CV3270362single nucleotide variantNM_144685.5(HIPK4):c.1047G>A (p.Met349Ile)not specified [RCV004397280]uncertain significance194038094440380944Humanname
405779053CV3270363single nucleotide variantNM_144685.5(HIPK4):c.1244G>A (p.Arg415Gln)not specified [RCV004397281]uncertain significance194038074740380747Humanname
407527273CV3437379single nucleotide variantNM_144685.5(HIPK4):c.1631A>G (p.Asp544Gly)not specified [RCV004632737]uncertain significance194038036040380360Humanname
597790247CV3682477single nucleotide variantNM_144685.5(HIPK4):c.1797T>A (p.His599Gln)not specified [RCV004933168]uncertain significance194037964140379641Humanname
597790251CV3682478single nucleotide variantNM_144685.5(HIPK4):c.1180T>C (p.Cys394Arg)not specified [RCV004933169]likely benign194038081140380811Humanname
597790259CV3682480single nucleotide variantNM_144685.5(HIPK4):c.1603C>T (p.Pro535Ser)not specified [RCV004933171]uncertain significance194038038840380388Humanname
597790267CV3682482single nucleotide variantNM_144685.5(HIPK4):c.1217G>A (p.Ser406Asn)not specified [RCV004933173]uncertain significance194038077440380774Humanname
598178271CV3978913single nucleotide variantNM_144685.5(HIPK4):c.1478C>T (p.Ala493Val)not specified [RCV005351962]uncertain significance194038051340380513Humanname
598178278CV3978914single nucleotide variantNM_144685.5(HIPK4):c.1840G>A (p.Gly614Arg)not specified [RCV005351963]uncertain significance194037959840379598Humanname
598248247CV3978920single nucleotide variantNM_144685.5(HIPK4):c.1099C>T (p.Arg367Cys)not specified [RCV005345415]uncertain significance194038089240380892Humanname
598248253CV3978922single nucleotide variantNM_144685.5(HIPK4):c.1631A>C (p.Asp544Ala)not specified [RCV005345416]uncertain significance194038036040380360Humanname
598178328CV3978924single nucleotide variantNM_144685.5(HIPK4):c.1330G>A (p.Glu444Lys)not specified [RCV005351970]uncertain significance194038066140380661Humanname
15102354CV704990single nucleotide variantNM_144685.5(HIPK4):c.1218T>G (p.Ser406Arg)not provided [RCV000959273]benign194038077340380773Humanname
15140036CV716448single nucleotide variantNM_144685.5(HIPK4):c.1261G>A (p.Gly421Ser)not provided [RCV000966071]benign194038073040380730Humanname