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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


71 records found for search term Fastkd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156000312CV2296296single nucleotide variantNM_024622.6(FASTKD1):c.13C>A (p.Pro5Thr)not specified [RCV004154197]uncertain significance2169572017169572017Humanname
405763492CV3253170single nucleotide variantNM_024622.6(FASTKD1):c.21C>A (p.Phe7Leu)not specified [RCV004383886]uncertain significance2169572009169572009Humanname
401775992CV2706842single nucleotide variantNM_024622.6(FASTKD1):c.61A>G (p.Ile21Val)not specified [RCV004321474]uncertain significance2169571969169571969Humanname
405763508CV3253173single nucleotide variantNM_024622.6(FASTKD1):c.49C>T (p.Arg17Cys)not specified [RCV004383889]uncertain significance2169571981169571981Humanname
156179066CV2287975single nucleotide variantNM_024622.6(FASTKD1):c.187C>T (p.Leu63Phe)not specified [RCV004147747]uncertain significance2169571843169571843Humanname
156195695CV2367160single nucleotide variantNM_024622.6(FASTKD1):c.247A>C (p.Thr83Pro)not specified [RCV004215594]uncertain significance2169571783169571783Humanname
156137456CV2375759single nucleotide variantNM_024622.6(FASTKD1):c.272A>G (p.Tyr91Cys)not specified [RCV004224350]likely benign2169571758169571758Humanname
329397450CV2456180single nucleotide variantNM_024622.6(FASTKD1):c.202G>A (p.Val68Met)not specified [RCV004273370]uncertain significance2169571828169571828Humanname
405763480CV3253168single nucleotide variantNM_024622.6(FASTKD1):c.182C>G (p.Ala61Gly)not specified [RCV004383884]uncertain significance2169571848169571848Humanname
405763486CV3253169single nucleotide variantNM_024622.6(FASTKD1):c.190T>G (p.Ser64Ala)not specified [RCV004383885]uncertain significance2169571840169571840Humanname
597695757CV3672182single nucleotide variantNM_024622.6(FASTKD1):c.163T>G (p.Phe55Val)not specified [RCV004915801]uncertain significance2169571867169571867Humanname
598213320CV3966156single nucleotide variantNM_024622.6(FASTKD1):c.268G>A (p.Glu90Lys)not specified [RCV005339241]uncertain significance2169571762169571762Humanname
156287779CV2229669single nucleotide variantNM_024622.6(FASTKD1):c.721G>T (p.Val241Phe)not specified [RCV004103478]uncertain significance2169560637169560637Humanname
156206727CV2249979single nucleotide variantNM_024622.6(FASTKD1):c.422C>T (p.Thr141Ile)not specified [RCV004122946]uncertain significance2169569208169569208Humanname
156063604CV2272368single nucleotide variantNM_024622.6(FASTKD1):c.314C>G (p.Ala105Gly)not specified [RCV004133294]uncertain significance2169571716169571716Humanname
155953770CV2274244single nucleotide variantNM_024622.6(FASTKD1):c.554A>C (p.Glu185Ala)not specified [RCV004136647]uncertain significance2169563243169563243Humanname
155980464CV2343509single nucleotide variantNM_024622.6(FASTKD1):c.815T>A (p.Leu272His)not specified [RCV004197576]uncertain significance2169560543169560543Humanname
329402307CV2454125single nucleotide variantNM_024622.6(FASTKD1):c.962A>G (p.Glu321Gly)not specified [RCV004265622]uncertain significance2169560396169560396Humanname
401874489CV2759234single nucleotide variantNM_024622.6(FASTKD1):c.598A>G (p.Ile200Val)not specified [RCV004335832]uncertain significance2169560760169560760Humanname
405763520CV3253175single nucleotide variantNM_024622.6(FASTKD1):c.605C>T (p.Ser202Phe)not specified [RCV004383891]uncertain significance2169560753169560753Humanname
405763527CV3253176single nucleotide variantNM_024622.6(FASTKD1):c.667A>G (p.Ile223Val)not specified [RCV004383892]uncertain significance2169560691169560691Humanname
598213302CV3966153single nucleotide variantNM_024622.6(FASTKD1):c.601T>C (p.Ser201Pro)not specified [RCV005339238]uncertain significance2169560757169560757Humanname
598213310CV3966154single nucleotide variantNM_024622.6(FASTKD1):c.731G>T (p.Arg244Leu)not specified [RCV005339239]uncertain significance2169560627169560627Humanname
598213315CV3966155single nucleotide variantNM_024622.6(FASTKD1):c.907C>G (p.Pro303Ala)not specified [RCV005339240]uncertain significance2169560451169560451Humanname
15153705CV719405duplicationNM_024622.6(FASTKD1):c.2406dup (p.Arg803fs)not provided [RCV000880064]benign2169530622169530623Humanname
156083682CV2244496single nucleotide variantNM_024622.6(FASTKD1):c.1791C>G (p.Cys597Trp)not specified [RCV004100453]uncertain significance2169544746169544746Humanname
156100008CV2294679single nucleotide variantNM_024622.6(FASTKD1):c.2342T>G (p.Phe781Cys)not specified [RCV004161926]uncertain significance2169530687169530687Humanname
155943463CV2298585single nucleotide variantNM_024622.6(FASTKD1):c.1024C>G (p.Leu342Val)not specified [RCV004162233]uncertain significance2169557245169557245Humanname
156151918CV2318849single nucleotide variantNM_024622.6(FASTKD1):c.2494A>G (p.Met832Val)not specified [RCV004175758]uncertain significance2169529875169529875Humanname
155972500CV2335807single nucleotide variantNM_024622.6(FASTKD1):c.1015G>A (p.Glu339Lys)not specified [RCV004193996]uncertain significance2169557254169557254Humanname
156123254CV2350006single nucleotide variantNM_024622.6(FASTKD1):c.1958C>T (p.Ser653Phe)not specified [RCV004199932]uncertain significance2169538129169538129Humanname
155989871CV2352288single nucleotide variantNM_024622.6(FASTKD1):c.2168C>T (p.Thr723Met)not specified [RCV004200763]uncertain significance2169537247169537247Humanname
156122443CV2354330single nucleotide variantNM_024622.6(FASTKD1):c.2249C>T (p.Ala750Val)not specified [RCV004206747]uncertain significance2169531430169531430Humanname
156172491CV2355083single nucleotide variantNM_024622.6(FASTKD1):c.2228C>T (p.Pro743Leu)not specified [RCV004198477]uncertain significance2169531451169531451Humanname
155937965CV2373913single nucleotide variantNM_024622.6(FASTKD1):c.1178A>C (p.Lys393Thr)not specified [RCV004224844]uncertain significance2169555160169555160Humanname
156039580CV2384277single nucleotide variantNM_024622.6(FASTKD1):c.1590T>A (p.Asp530Glu)not specified [RCV004227664]likely benign2169546329169546329Humanname
155907865CV2387139single nucleotide variantNM_024622.6(FASTKD1):c.2096C>T (p.Thr699Ile)not specified [RCV004238248]uncertain significance2169537319169537319Humanname
329370910CV2431807single nucleotide variantNM_024622.6(FASTKD1):c.2089G>A (p.Asp697Asn)not specified [RCV004254954]likely benign2169537326169537326Humanname
329361027CV2436603single nucleotide variantNM_024622.6(FASTKD1):c.1262G>A (p.Arg421His)not specified [RCV004257983]uncertain significance2169546657169546657Humanname
329392978CV2449418single nucleotide variantNM_024622.6(FASTKD1):c.1730T>C (p.Ile577Thr)not specified [RCV004266578]uncertain significance2169544807169544807Humanname
401743257CV2674616single nucleotide variantNM_024622.6(FASTKD1):c.2240A>G (p.His747Arg)not specified [RCV004293920]uncertain significance2169531439169531439Humanname
401772189CV2708190single nucleotide variantNM_024622.6(FASTKD1):c.1502G>A (p.Arg501Gln)not specified [RCV004311550]uncertain significance2169546417169546417Humanname
401765655CV2717795single nucleotide variantNM_024622.6(FASTKD1):c.2051G>A (p.Arg684His)not specified [RCV004321779]uncertain significance2169538036169538036Humanname
401883619CV2754511single nucleotide variantNM_024622.6(FASTKD1):c.2533T>C (p.Ser845Pro)not specified [RCV004336718]uncertain significance2169529836169529836Humanname
401878468CV2770561single nucleotide variantNM_024622.6(FASTKD1):c.1160T>C (p.Phe387Ser)not specified [RCV004349628]uncertain significance2169555178169555178Humanname
405763433CV3253160single nucleotide variantNM_024622.6(FASTKD1):c.1037G>A (p.Gly346Glu)not specified [RCV004383876]uncertain significance2169557232169557232Humanname
405763439CV3253161single nucleotide variantNM_024622.6(FASTKD1):c.1053G>A (p.Met351Ile)not specified [RCV004383877]uncertain significance2169557216169557216Humanname
405763445CV3253162single nucleotide variantNM_024622.6(FASTKD1):c.1144A>C (p.Thr382Pro)not specified [RCV004383878]uncertain significance2169555194169555194Humanname
405763452CV3253163single nucleotide variantNM_024622.6(FASTKD1):c.1249T>C (p.Ser417Pro)not specified [RCV004383879]uncertain significance2169546670169546670Humanname
405763456CV3253164single nucleotide variantNM_024622.6(FASTKD1):c.1270T>C (p.Ser424Pro)not specified [RCV004383880]uncertain significance2169546649169546649Humanname
405763462CV3253165single nucleotide variantNM_024622.6(FASTKD1):c.1313G>A (p.Arg438Gln)not specified [RCV004383881]uncertain significance2169546606169546606Humanname
405763469CV3253166single nucleotide variantNM_024622.6(FASTKD1):c.1477C>T (p.His493Tyr)not specified [RCV004383882]uncertain significance2169546442169546442Humanname
405763474CV3253167single nucleotide variantNM_024622.6(FASTKD1):c.1564G>A (p.Ala522Thr)not specified [RCV004383883]uncertain significance2169546355169546355Humanname
405763499CV3253171single nucleotide variantNM_024622.6(FASTKD1):c.2325A>C (p.Glu775Asp)not specified [RCV004383887]uncertain significance2169531354169531354Humanname
405763504CV3253172single nucleotide variantNM_024622.6(FASTKD1):c.2441A>G (p.Gln814Arg)not specified [RCV004383888]uncertain significance2169530588169530588Humanname
407492716CV3432160single nucleotide variantNM_024622.6(FASTKD1):c.1425A>T (p.Lys475Asn)not specified [RCV004620858]uncertain significance2169546494169546494Humanname
407492720CV3432161single nucleotide variantNM_024622.6(FASTKD1):c.1094T>G (p.Val365Gly)not specified [RCV004620859]uncertain significance2169555244169555244Humanname
597695730CV3672179single nucleotide variantNM_024622.6(FASTKD1):c.1841T>C (p.Val614Ala)not specified [RCV004915798]uncertain significance2169540155169540155Humanname
597695740CV3672180single nucleotide variantNM_024622.6(FASTKD1):c.1501C>T (p.Arg501Trp)not specified [RCV004915799]likely benign2169546418169546418Humanname
597695750CV3672181single nucleotide variantNM_024622.6(FASTKD1):c.2105A>G (p.Gln702Arg)not specified [RCV004915800]uncertain significance2169537310169537310Humanname
597695765CV3672183single nucleotide variantNM_024622.6(FASTKD1):c.1862C>A (p.Ala621Asp)not specified [RCV004915802]uncertain significance2169540134169540134Humanname
597695771CV3672184single nucleotide variantNM_024622.6(FASTKD1):c.1622C>G (p.Ser541Cys)not specified [RCV004915803]uncertain significance2169546297169546297Humanname
597695779CV3672185single nucleotide variantNM_024622.6(FASTKD1):c.1354A>G (p.Ser452Gly)not specified [RCV004915804]uncertain significance2169546565169546565Humanname
597695789CV3672186single nucleotide variantNM_024622.6(FASTKD1):c.1868T>C (p.Leu623Pro)not specified [RCV004915805]uncertain significance2169540128169540128Humanname
597695797CV3672187single nucleotide variantNM_024622.6(FASTKD1):c.1613A>G (p.Glu538Gly)not specified [RCV004915806]likely benign2169546306169546306Humanname
598213283CV3966149single nucleotide variantNM_024622.6(FASTKD1):c.1732C>T (p.Arg578Cys)not specified [RCV005339235]uncertain significance2169544805169544805Humanname
598213288CV3966150single nucleotide variantNM_024622.6(FASTKD1):c.2359C>A (p.Leu787Ile)not specified [RCV005339236]uncertain significance2169530670169530670Humanname
598213294CV3966151single nucleotide variantNM_024622.6(FASTKD1):c.2491C>T (p.Arg831Trp)not specified [RCV005339237]uncertain significance2169529878169529878Humanname
598271519CV3966152single nucleotide variantNM_024622.6(FASTKD1):c.1479C>G (p.His493Gln)not specified [RCV005327762]uncertain significance2169546440169546440Humanname
13706973CV539434single nucleotide variantNM_024622.6(FASTKD1):c.2230T>A (p.Tyr744Asn)Glaucoma 1, open angle, B [RCV000663362]pathogenic2169531449169531449Human1name
15187758CV697157single nucleotide variantNM_024622.6(FASTKD1):c.2303C>G (p.Ser768Ter)not provided [RCV000953682]benign2169531376169531376Humanname