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61 records found for search term Paox
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401928732CV2806344single nucleotide variantNM_152911.4(PAOX):c.282G>A (p.Glu94=)not provided [RCV003389972]likely benign10133380099133380099Humanname
598259223CV4005806single nucleotide variantNM_152911.4(PAOX):c.25G>A (p.Glu9Lys)not specified [RCV005386442]likely benign10133379341133379341Humanname
401763059CV2720180single nucleotide variantNM_152911.4(PAOX):c.74G>T (p.Gly25Val)not specified [RCV004323733]uncertain significance10133379390133379390Humanname
156293974CV2321368single nucleotide variantNM_152911.4(PAOX):c.128T>C (p.Val43Ala)not specified [RCV004177367]uncertain significance10133379444133379444Humanname
156342267CV2343819single nucleotide variantNM_152911.4(PAOX):c.164G>A (p.Arg55His)not specified [RCV004193405]uncertain significance10133379480133379480Humanname
401756118CV2686296single nucleotide variantNM_152911.4(PAOX):c.163C>T (p.Arg55Cys)not specified [RCV004297379]uncertain significance10133379479133379479Humanname
401756409CV2687134single nucleotide variantNM_152911.4(PAOX):c.100G>T (p.Gly34Cys)not specified [RCV004304438]uncertain significance10133379416133379416Humanname
401758098CV2731686single nucleotide variantNM_152911.4(PAOX):c.1449C>T (p.His483=)not specified [RCV004331790]likely benign10133391368133391368Humanname
401890974CV2778571single nucleotide variantNM_152911.4(PAOX):c.1152C>T (p.Ala384=)not specified [RCV004344222]likely benign10133388986133388986Humanname
405758995CV3364093single nucleotide variantNM_152911.4(PAOX):c.1200T>C (p.Leu400=)not specified [RCV004500294]likely benign10133389034133389034Humanname
405759017CV3364097single nucleotide variantNM_152911.4(PAOX):c.1431G>A (p.Thr477=)not specified [RCV004500298]likely benign10133391350133391350Humanname
405759023CV3364098single nucleotide variantNM_152911.4(PAOX):c.187G>A (p.Val63Met)not specified [RCV004500299]uncertain significance10133380004133380004Humanname
405759030CV3364099single nucleotide variantNM_152911.4(PAOX):c.227G>T (p.Arg76Leu)not specified [RCV004500300]uncertain significance10133380044133380044Humanname
407518001CV3466442single nucleotide variantNM_152911.4(PAOX):c.1446G>A (p.Thr482=)not specified [RCV004650852]likely benign10133391365133391365Humanname
597717369CV3571223single nucleotide variantNM_152911.4(PAOX):c.157C>T (p.Arg53Cys)not specified [RCV004841524]uncertain significance10133379473133379473Humanname
598259213CV4005804single nucleotide variantNM_152911.4(PAOX):c.1401C>T (p.Ile467=)not specified [RCV005386440]likely benign10133391320133391320Humanname
598184993CV4005808single nucleotide variantNM_152911.4(PAOX):c.104A>G (p.His35Arg)not specified [RCV005395537]uncertain significance10133379420133379420Humanname
598185008CV4005811single nucleotide variantNM_152911.4(PAOX):c.1410G>T (p.Ala470=)not specified [RCV005395539]likely benign10133391329133391329Humanname
156161187CV2272570single nucleotide variantNM_152911.4(PAOX):c.406G>A (p.Gly136Ser)not specified [RCV004133460]uncertain significance10133380223133380223Humanname
156106537CV2307658single nucleotide variantNM_152911.4(PAOX):c.670G>A (p.Gly224Ser)not specified [RCV004168075]uncertain significance10133381461133381461Humanname
329357633CV2427787single nucleotide variantNM_152911.4(PAOX):c.383C>T (p.Ala128Val)not specified [RCV004252565]uncertain significance10133380200133380200Humanname
401751554CV2672494single nucleotide variantNM_152911.4(PAOX):c.806C>T (p.Ser269Leu)not specified [RCV004287534]likely benign10133381597133381597Humanname
401778931CV2701887single nucleotide variantNM_152911.4(PAOX):c.874C>A (p.Leu292Ile)not specified [RCV004320507]uncertain significance10133383965133383965Humanname
401765218CV2712548single nucleotide variantNM_152911.4(PAOX):c.987G>T (p.Glu329Asp)not provided [RCV004696456]|not specified [RCV004307882]uncertain significance10133384078133384078Humanname
401765594CV2717772single nucleotide variantNM_152911.4(PAOX):c.392C>G (p.Ala131Gly)not specified [RCV004321757]uncertain significance10133380209133380209Humanname
405759037CV3364100single nucleotide variantNM_152911.4(PAOX):c.346G>T (p.Ala116Ser)not specified [RCV004500301]uncertain significance10133380163133380163Humanname
405759049CV3364102single nucleotide variantNM_152911.4(PAOX):c.812A>G (p.Glu271Gly)not specified [RCV004500303]uncertain significance10133381603133381603Humanname
405759053CV3364103single nucleotide variantNM_152911.4(PAOX):c.863C>T (p.Pro288Leu)not specified [RCV004500304]uncertain significance10133381654133381654Humanname
407479461CV3466440single nucleotide variantNM_152911.4(PAOX):c.337G>A (p.Val113Met)not specified [RCV004664139]uncertain significance10133380154133380154Humanname
407479466CV3466441single nucleotide variantNM_152911.4(PAOX):c.447G>T (p.Glu149Asp)not specified [RCV004664140]uncertain significance10133380264133380264Humanname
597717329CV3571219single nucleotide variantNM_152911.4(PAOX):c.643C>T (p.Pro215Ser)not specified [RCV004841520]uncertain significance10133380460133380460Humanname
597717357CV3571222single nucleotide variantNM_152911.4(PAOX):c.736C>T (p.Pro246Ser)not specified [RCV004841523]uncertain significance10133381527133381527Humanname
597717377CV3571225single nucleotide variantNM_152911.4(PAOX):c.586G>A (p.Gly196Ser)not specified [RCV004841525]uncertain significance10133380403133380403Humanname
598259204CV4005802single nucleotide variantNM_152911.4(PAOX):c.332C>T (p.Pro111Leu)not specified [RCV005386438]uncertain significance10133380149133380149Humanname
598259207CV4005803single nucleotide variantNM_152911.4(PAOX):c.527C>T (p.Thr176Ile)not specified [RCV005386439]uncertain significance10133380344133380344Humanname
598185000CV4005809single nucleotide variantNM_152911.4(PAOX):c.482A>G (p.Lys161Arg)not specified [RCV005395538]uncertain significance10133380299133380299Humanname
598259233CV4005810single nucleotide variantNM_152911.4(PAOX):c.467G>A (p.Gly156Glu)not specified [RCV005386444]uncertain significance10133380284133380284Humanname
598259236CV4005812single nucleotide variantNM_152911.4(PAOX):c.557C>T (p.Ser186Phe)not specified [RCV005386445]uncertain significance10133380374133380374Humanname
156240475CV2231278single nucleotide variantNM_152911.4(PAOX):c.1222C>T (p.Arg408Trp)not specified [RCV004094763]uncertain significance10133389056133389056Humanname
155929186CV2277991single nucleotide variantNM_152911.4(PAOX):c.1071G>C (p.Gln357His)not specified [RCV004141228]uncertain significance10133384162133384162Humanname
156117592CV2278881single nucleotide variantNM_152911.4(PAOX):c.1276C>T (p.Arg426Cys)not specified [RCV004145584]likely benign10133389631133389631Humanname
155903039CV2353505single nucleotide variantNM_152911.4(PAOX):c.1008C>G (p.Cys336Trp)not specified [RCV004199490]uncertain significance10133384099133384099Humanname
156451076CV2402453single nucleotide variantNM_152911.4(PAOX):c.1360C>G (p.Gln454Glu)not provided [RCV003123254]uncertain significance10133389715133389715Humanname
329388054CV2437083single nucleotide variantNM_152911.4(PAOX):c.1270C>T (p.Arg424Trp)not specified [RCV004262891]uncertain significance10133389625133389625Humanname
329387961CV2440283single nucleotide variantNM_152911.4(PAOX):c.1010A>G (p.Gln337Arg)not specified [RCV004262768]uncertain significance10133384101133384101Humanname
401720696CV2673435single nucleotide variantNM_152911.4(PAOX):c.1445C>T (p.Thr482Met)not specified [RCV004288409]uncertain significance10133391364133391364Humanname
401722026CV2680790single nucleotide variantNM_152911.4(PAOX):c.1384G>A (p.Gly462Ser)not specified [RCV004293440]uncertain significance10133389739133389739Humanname
401734559CV2688558single nucleotide variantNM_152911.4(PAOX):c.1142G>A (p.Gly381Glu)not specified [RCV004301518]uncertain significance10133388976133388976Humanname
401719027CV2704925single nucleotide variantNM_152911.4(PAOX):c.1483C>T (p.Arg495Cys)not specified [RCV004307496]uncertain significance10133391402133391402Humanname
401880661CV2780309single nucleotide variantNM_152911.4(PAOX):c.1310A>C (p.Tyr437Ser)not specified [RCV004355930]uncertain significance10133389665133389665Humanname
405758984CV3364091single nucleotide variantNM_152911.4(PAOX):c.1094T>C (p.Ile365Thr)not specified [RCV004500292]uncertain significance10133384185133384185Humanname
405758990CV3364092single nucleotide variantNM_152911.4(PAOX):c.1172T>C (p.Met391Thr)not specified [RCV004500293]uncertain significance10133389006133389006Humanname
405759005CV3364095single nucleotide variantNM_152911.4(PAOX):c.1381G>A (p.Ala461Thr)not specified [RCV004500296]likely benign10133389736133389736Humanname
405759012CV3364096single nucleotide variantNM_152911.4(PAOX):c.1394T>A (p.Leu465His)not specified [RCV004500297]uncertain significance10133391313133391313Humanname
597717338CV3571220single nucleotide variantNM_152911.4(PAOX):c.1243C>T (p.Arg415Trp)not specified [RCV004841521]uncertain significance10133389598133389598Humanname
597717347CV3571221single nucleotide variantNM_152911.4(PAOX):c.1180C>G (p.Leu394Val)not specified [RCV004841522]uncertain significance10133389014133389014Humanname
597657828CV3571224single nucleotide variantNM_152911.4(PAOX):c.1250C>T (p.Pro417Leu)not specified [RCV004827681]uncertain significance10133389605133389605Humanname
597657837CV3571226single nucleotide variantNM_152911.4(PAOX):c.1450G>A (p.Gly484Arg)not specified [RCV004827682]uncertain significance10133391369133391369Humanname
598259198CV4005801single nucleotide variantNM_152911.4(PAOX):c.1204T>C (p.Cys402Arg)not specified [RCV005386437]uncertain significance10133389038133389038Humanname
598259218CV4005805single nucleotide variantNM_152911.4(PAOX):c.1484G>A (p.Arg495His)not specified [RCV005386441]uncertain significance10133391403133391403Humanname
598259228CV4005807single nucleotide variantNM_152911.4(PAOX):c.1480G>A (p.Asp494Asn)not specified [RCV005386443]uncertain significance10133391399133391399Humanname