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Variants search result for Homo sapiens
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51 records found for search term Apeh
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401763552CV2720364single nucleotide variantNM_001640.4(APEH):c.80G>T (p.Ser27Ile)not specified [RCV004325677]uncertain significance34967455649674556Humanname
401926428CV2827429single nucleotide variantNM_001640.4(APEH):c.561C>T (p.Ser187=)not provided [RCV003437848]likely benign34967617449676174Humanname
405662053CV3289693single nucleotide variantNM_001640.4(APEH):c.58C>A (p.Leu20Ile)not specified [RCV004417636]uncertain significance34967453449674534Humanname
401725422CV2697405single nucleotide variantNM_001640.4(APEH):c.266G>C (p.Arg89Pro)not specified [RCV004304155]uncertain significance34967530349675303Humanname
401882027CV2784043single nucleotide variantNM_001640.4(APEH):c.229G>A (p.Val77Met)not specified [RCV004362446]uncertain significance34967526649675266Humanname
401926429CV2827430single nucleotide variantNM_001640.4(APEH):c.1965G>A (p.Ser655=)not provided [RCV003437849]likely benign34968292449682924Humanname
597695638CV3574646single nucleotide variantNM_001640.4(APEH):c.265C>T (p.Arg89Trp)not specified [RCV004839144]uncertain significance34967530249675302Humanname
156242232CV2306491single nucleotide variantNM_001640.4(APEH):c.727A>C (p.Asn243His)not specified [RCV004157109]uncertain significance34967649849676498Humanname
156192756CV2350432single nucleotide variantNM_001640.4(APEH):c.334A>C (p.Thr112Pro)not specified [RCV004204806]uncertain significance34967575549675755Humanname
329359939CV2462213single nucleotide variantNM_001640.4(APEH):c.815T>A (p.Ile272Asn)not specified [RCV004266220]uncertain significance34967667949676679Humanname
401759985CV2701821single nucleotide variantNM_001640.4(APEH):c.938G>T (p.Arg313Leu)not specified [RCV004314210]uncertain significance34967696349676963Humanname
401752645CV2707078single nucleotide variantNM_001640.4(APEH):c.401A>G (p.Asn134Ser)not specified [RCV004321662]uncertain significance34967592549675925Humanname
401874067CV2772819single nucleotide variantNM_001640.4(APEH):c.916C>T (p.Arg306Trp)not specified [RCV004357607]uncertain significance34967694149676941Humanname
401868198CV2784685single nucleotide variantNM_001640.4(APEH):c.872A>C (p.Lys291Thr)not specified [RCV004352500]uncertain significance34967681249676812Humanname
401892392CV2785380single nucleotide variantNM_001640.4(APEH):c.567T>A (p.Asp189Glu)not specified [RCV004357124]uncertain significance34967618049676180Humanname
405662051CV3289692single nucleotide variantNM_001640.4(APEH):c.323A>G (p.Lys108Arg)not specified [RCV004417635]uncertain significance34967574449675744Humanname
407530626CV3463459single nucleotide variantNM_001640.4(APEH):c.830A>G (p.Asn277Ser)not specified [RCV004657151]uncertain significance34967669449676694Humanname
407511847CV3463468single nucleotide variantNM_001640.4(APEH):c.335C>T (p.Thr112Met)not specified [RCV004648182]uncertain significance34967575649675756Humanname
597695602CV3574641single nucleotide variantNM_001640.4(APEH):c.319C>T (p.Arg107Cys)not specified [RCV004839141]uncertain significance34967574049675740Humanname
597695613CV3574642single nucleotide variantNM_001640.4(APEH):c.832C>T (p.Arg278Cys)not specified [RCV004839142]uncertain significance34967669649676696Humanname
598241799CV4005168single nucleotide variantNM_001640.4(APEH):c.833G>A (p.Arg278His)not specified [RCV005383317]uncertain significance34967669749676697Humanname
598241889CV4005186single nucleotide variantNM_001640.4(APEH):c.382C>G (p.Arg128Gly)not specified [RCV005383331]uncertain significance34967590649675906Humanname
156140752CV2199881single nucleotide variantNM_001640.4(APEH):c.1378G>A (p.Asp460Asn)not specified [RCV004074070]uncertain significance34968117949681179Humanname
155940002CV2221915single nucleotide variantNM_001640.4(APEH):c.1846A>T (p.Ile616Phe)not specified [RCV004102927]uncertain significance34968269949682699Humanname
156053805CV2243010single nucleotide variantNM_001640.4(APEH):c.1433A>C (p.Gln478Pro)not specified [RCV004109931]uncertain significance34968123449681234Humanname
156315823CV2250827single nucleotide variantNM_001640.4(APEH):c.1579A>C (p.Lys527Gln)not specified [RCV004129685]uncertain significance34968194349681943Humanname
156319366CV2260832single nucleotide variantNM_001640.4(APEH):c.1727T>G (p.Phe576Cys)not specified [RCV004125742]uncertain significance34968258049682580Humanname
156189733CV2328854single nucleotide variantNM_001640.4(APEH):c.1597C>A (p.Leu533Ile)not specified [RCV004178068]uncertain significance34968196149681961Humanname
156165529CV2330054single nucleotide variantNM_001640.4(APEH):c.1724A>G (p.His575Arg)not specified [RCV004185546]uncertain significance34968257749682577Humanname
156333609CV2336021single nucleotide variantNM_001640.4(APEH):c.2078G>A (p.Arg693Gln)not specified [RCV004189626]uncertain significance34968313149683131Humanname
155919140CV2360153single nucleotide variantNM_001640.4(APEH):c.2027G>A (p.Arg676Gln)not specified [RCV004215425]uncertain significance34968308049683080Humanname
329372385CV2455185single nucleotide variantNM_001640.4(APEH):c.1162C>G (p.Leu388Val)not specified [RCV004274419]uncertain significance34967959649679596Humanname
401773574CV2727565single nucleotide variantNM_001640.4(APEH):c.1573C>G (p.Leu525Val)not specified [RCV004329753]uncertain significance34968193749681937Humanname
401765383CV2733666single nucleotide variantNM_001640.4(APEH):c.1062G>T (p.Glu354Asp)not specified [RCV004330462]uncertain significance34967885349678853Humanname
405662039CV3289688single nucleotide variantNM_001640.4(APEH):c.1122G>C (p.Gln374His)not specified [RCV004417631]uncertain significance34967891349678913Humanname
405662042CV3289689single nucleotide variantNM_001640.4(APEH):c.1415C>T (p.Pro472Leu)not specified [RCV004417632]uncertain significance34968121649681216Humanname
405662046CV3289690single nucleotide variantNM_001640.4(APEH):c.1798T>C (p.Tyr600His)not specified [RCV004417633]uncertain significance34968265149682651Humanname
405662048CV3289691single nucleotide variantNM_001640.4(APEH):c.2159T>C (p.Met720Thr)not specified [RCV004417634]uncertain significance34968330249683302Humanname
597657270CV3574639single nucleotide variantNM_001640.4(APEH):c.2156T>C (p.Phe719Ser)not specified [RCV004827603]uncertain significance34968329949683299Humanname
597695627CV3574643single nucleotide variantNM_001640.4(APEH):c.1613G>A (p.Arg538His)not specified [RCV004839143]uncertain significance34968235749682357Humanname
597657276CV3574645single nucleotide variantNM_001640.4(APEH):c.1295C>A (p.Thr432Asn)not specified [RCV004827604]uncertain significance34968062549680625Humanname
597695644CV3574647single nucleotide variantNM_001640.4(APEH):c.1808C>T (p.Thr603Ile)not specified [RCV004839145]uncertain significance34968266149682661Humanname
597695657CV3574648single nucleotide variantNM_001640.4(APEH):c.1748T>C (p.Leu583Pro)not specified [RCV004839146]uncertain significance34968260149682601Humanname
597695670CV3574649single nucleotide variantNM_001640.4(APEH):c.1820G>C (p.Cys607Ser)not specified [RCV004839147]uncertain significance34968267349682673Humanname
597657283CV3574650single nucleotide variantNM_001640.4(APEH):c.1078T>C (p.Tyr360His)not specified [RCV004827605]uncertain significance34967886949678869Humanname
598182886CV4005130single nucleotide variantNM_001640.4(APEH):c.1220G>T (p.Gly407Val)not specified [RCV005395213]uncertain significance34968055049680550Humanname
598241668CV4005139single nucleotide variantNM_001640.4(APEH):c.1147C>T (p.Arg383Cys)not specified [RCV005383292]uncertain significance34967893849678938Humanname
598241695CV4005148single nucleotide variantNM_001640.4(APEH):c.1366G>A (p.Glu456Lys)not specified [RCV005383297]uncertain significance34968116749681167Humanname
598241748CV4005158single nucleotide variantNM_001640.4(APEH):c.1700T>C (p.Val567Ala)not specified [RCV005383307]uncertain significance34968255349682553Humanname
598241840CV4005177single nucleotide variantNM_001640.4(APEH):c.1375C>T (p.Pro459Ser)not specified [RCV005383323]uncertain significance34968117649681176Humanname
598241963CV4005198single nucleotide variantNM_001640.4(APEH):c.1492A>G (p.Thr498Ala)not specified [RCV005383342]uncertain significance34968177549681775Humanname