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Variants search result for Homo sapiens
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48 records found for search term Cpa5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401730843CV2711526single nucleotide variantNM_080385.5(CPA5):c.26C>G (p.Thr9Arg)not specified [RCV004306841]uncertain significance7130346511130346511Humanname
156173969CV2247636single nucleotide variantNM_080385.5(CPA5):c.95T>G (p.Leu32Trp)not specified [RCV004110970]likely benign7130346580130346580Humanname
405685985CV3235823single nucleotide variantNM_080385.5(CPA5):c.55C>G (p.Arg19Gly)not specified [RCV004372337]uncertain significance7130346540130346540Humanname
156165709CV2330068single nucleotide variantNM_080385.5(CPA5):c.233T>C (p.Leu78Pro)not specified [RCV004185560]uncertain significance7130350009130350009Humanname
155926925CV2365845single nucleotide variantNM_080385.5(CPA5):c.131G>A (p.Arg44Gln)not specified [RCV004214379]uncertain significance7130347780130347780Humanname
156260605CV2395561single nucleotide variantNM_080385.5(CPA5):c.212G>A (p.Arg71His)not specified [RCV004241414]uncertain significance7130349988130349988Humanname
405685951CV3235816single nucleotide variantNM_080385.5(CPA5):c.1227G>A (p.Pro409=)not specified [RCV004372330]likely benign7130368513130368513Humanname
405685954CV3235817single nucleotide variantNM_080385.5(CPA5):c.1248G>A (p.Thr416=)not specified [RCV004372331]likely benign7130368534130368534Humanname
405685959CV3235818single nucleotide variantNM_080385.5(CPA5):c.250G>A (p.Val84Ile)not specified [RCV004372332]uncertain significance7130350026130350026Humanname
597650206CV3650926single nucleotide variantNM_080385.5(CPA5):c.1260G>A (p.Thr420=)not specified [RCV004910434]likely benign7130368546130368546Humanname
597773992CV3650931single nucleotide variantNM_080385.5(CPA5):c.224G>A (p.Arg75Lys)not specified [RCV004897626]uncertain significance7130350000130350000Humanname
598235208CV3945142single nucleotide variantNM_080385.5(CPA5):c.229A>G (p.Ser77Gly)not specified [RCV005320209]uncertain significance7130350005130350005Humanname
156230622CV2199588single nucleotide variantNM_080385.5(CPA5):c.877C>G (p.His293Asp)not specified [RCV004072336]uncertain significance7130367410130367410Humanname
156126401CV2234356single nucleotide variantNM_080385.5(CPA5):c.959T>C (p.Ile320Thr)not specified [RCV004100586]uncertain significance7130367492130367492Humanname
156199313CV2255981single nucleotide variantNM_080385.5(CPA5):c.479T>C (p.Val160Ala)not specified [RCV004122427]uncertain significance7130361189130361189Humanname
155964958CV2330515single nucleotide variantNM_080385.5(CPA5):c.896C>T (p.Ser299Leu)not specified [RCV004181079]uncertain significance7130367429130367429Humanname
155972698CV2335833single nucleotide variantNM_080385.5(CPA5):c.760C>T (p.Arg254Trp)not specified [RCV004196067]uncertain significance7130363431130363431Humanname
156053742CV2388558single nucleotide variantNM_080385.5(CPA5):c.799G>A (p.Gly267Ser)not specified [RCV004237406]uncertain significance7130363470130363470Humanname
329387439CV2436467single nucleotide variantNM_080385.5(CPA5):c.377G>A (p.Arg126Gln)not specified [RCV004251847]uncertain significance7130359632130359632Humanname
401729130CV2673162single nucleotide variantNM_080385.5(CPA5):c.386G>A (p.Arg129His)not specified [RCV004284143]uncertain significance7130359641130359641Humanname
401726961CV2691916single nucleotide variantNM_080385.5(CPA5):c.595G>A (p.Glu199Lys)not specified [RCV004299652]uncertain significance7130362498130362498Humanname
401730619CV2711417single nucleotide variantNM_080385.5(CPA5):c.563C>T (p.Ala188Val)not specified [RCV004313169]uncertain significance7130362466130362466Humanname
401890220CV2763711single nucleotide variantNM_080385.5(CPA5):c.859C>T (p.Pro287Ser)not specified [RCV004343207]uncertain significance7130367392130367392Humanname
405685964CV3235819single nucleotide variantNM_080385.5(CPA5):c.317T>C (p.Met106Thr)not specified [RCV004372333]uncertain significance7130350093130350093Humanname
405685968CV3235820single nucleotide variantNM_080385.5(CPA5):c.495T>G (p.Ile165Met)not specified [RCV004372334]uncertain significance7130361205130361205Humanname
405685974CV3235821single nucleotide variantNM_080385.5(CPA5):c.553C>T (p.Arg185Trp)not specified [RCV004372335]uncertain significance7130362456130362456Humanname
405685980CV3235822single nucleotide variantNM_080385.5(CPA5):c.554G>A (p.Arg185Gln)not specified [RCV004372336]likely benign7130362457130362457Humanname
405685995CV3235825single nucleotide variantNM_080385.5(CPA5):c.701T>C (p.Ile234Thr)not specified [RCV004372339]uncertain significance7130362948130362948Humanname
405686000CV3235826single nucleotide variantNM_080385.5(CPA5):c.925T>C (p.Phe309Leu)not specified [RCV004372340]uncertain significance7130367458130367458Humanname
407457219CV3419553single nucleotide variantNM_080385.5(CPA5):c.376C>T (p.Arg126Trp)not specified [RCV004610947]uncertain significance7130359631130359631Humanname
597650197CV3650925single nucleotide variantNM_080385.5(CPA5):c.691G>A (p.Asp231Asn)not specified [RCV004910433]uncertain significance7130362938130362938Humanname
597650247CV3650932single nucleotide variantNM_080385.5(CPA5):c.822G>C (p.Trp274Cys)not specified [RCV004910439]uncertain significance7130363493130363493Humanname
597650257CV3650933single nucleotide variantNM_080385.5(CPA5):c.686C>T (p.Ala229Val)not specified [RCV004910440]uncertain significance7130362933130362933Humanname
598235216CV3945143single nucleotide variantNM_080385.5(CPA5):c.559C>T (p.Pro187Ser)not specified [RCV005320210]uncertain significance7130362462130362462Humanname
156370692CV2204291single nucleotide variantNM_080385.5(CPA5):c.1067C>T (p.Ala356Val)not specified [RCV004079119]uncertain significance7130367934130367934Humanname
156167367CV2237228single nucleotide variantNM_080385.5(CPA5):c.1156T>C (p.Tyr386His)not specified [RCV004114961]uncertain significance7130368442130368442Humanname
156173950CV2247635single nucleotide variantNM_080385.5(CPA5):c.1178C>A (p.Ala393Asp)not specified [RCV004599474]uncertain significance7130368464130368464Humanname
156276089CV2276704single nucleotide variantNM_080385.5(CPA5):c.1196G>A (p.Arg399Gln)not specified [RCV004146500]uncertain significance7130368482130368482Humanname
156200817CV2313104single nucleotide variantNM_080385.5(CPA5):c.1015C>T (p.Pro339Ser)not specified [RCV004161375]uncertain significance7130367548130367548Humanname
329375134CV2470893single nucleotide variantNM_080385.5(CPA5):c.1043A>G (p.Asp348Gly)not specified [RCV004276092]uncertain significance7130367910130367910Humanname
401736151CV2688715single nucleotide variantNM_080385.5(CPA5):c.1268C>T (p.Ala423Val)not specified [RCV004303752]uncertain significance7130368554130368554Humanname
401760304CV2709743single nucleotide variantNM_080385.5(CPA5):c.1279A>G (p.Ile427Val)not specified [RCV004320733]uncertain significance7130368565130368565Humanname
407457222CV3419552single nucleotide variantNM_080385.5(CPA5):c.1118C>T (p.Thr373Ile)not specified [RCV004610946]uncertain significance7130367985130367985Humanname
597650214CV3650927single nucleotide variantNM_080385.5(CPA5):c.1162A>G (p.Ser388Gly)not specified [RCV004910435]uncertain significance7130368448130368448Humanname
597650226CV3650928single nucleotide variantNM_080385.5(CPA5):c.1174T>A (p.Tyr392Asn)not specified [RCV004910436]uncertain significance7130368460130368460Humanname
597650233CV3650929single nucleotide variantNM_080385.5(CPA5):c.1177G>A (p.Ala393Thr)not specified [RCV004910437]uncertain significance7130368463130368463Humanname
597650242CV3650930single nucleotide variantNM_080385.5(CPA5):c.1073A>G (p.Tyr358Cys)not specified [RCV004910438]uncertain significance7130367940130367940Humanname
597650266CV3650934single nucleotide variantNM_080385.5(CPA5):c.1202C>A (p.Thr401Asn)not specified [RCV004910441]uncertain significance7130368488130368488Humanname