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Variants search result for Homo sapiens
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32 records found for search term Klk5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156340271CV2347819single nucleotide variantNM_012427.5(KLK5):c.16C>T (p.Pro6Ser)not specified [RCV004195474]uncertain significance195095264250952642Humanname
155998257CV2260958single nucleotide variantNM_012427.5(KLK5):c.35T>C (p.Leu12Pro)not specified [RCV004125839]uncertain significance195095262350952623Humanname
329393910CV2472202single nucleotide variantNM_012427.5(KLK5):c.48C>G (p.Ile16Met)not specified [RCV004283320]uncertain significance195095261050952610Humanname
405814063CV3276422single nucleotide variantNM_012427.5(KLK5):c.58C>G (p.Leu20Val)not specified [RCV004409658]uncertain significance195095260050952600Humanname
405814056CV3276425single nucleotide variantNM_012427.5(KLK5):c.65G>T (p.Gly22Val)not specified [RCV004409661]uncertain significance195095259350952593Humanname
405813979CV3276429single nucleotide variantNM_012427.5(KLK5):c.77A>G (p.His26Arg)not specified [RCV004409665]likely benign195095011350950113Humanname
156167266CV2200993single nucleotide variantNM_012427.5(KLK5):c.214G>A (p.Asp72Asn)not specified [RCV004074759]uncertain significance195094997650949976Humanname
156032292CV2275004single nucleotide variantNM_012427.5(KLK5):c.161C>T (p.Ala54Val)not specified [RCV004135047]uncertain significance195095002950950029Humanname
155996428CV2288510single nucleotide variantNM_012427.5(KLK5):c.293T>C (p.Val98Ala)not specified [RCV004152044]uncertain significance195094989750949897Humanname
407499061CV3448685single nucleotide variantNM_012427.5(KLK5):c.238T>C (p.Trp80Arg)not specified [RCV004644216]uncertain significance195094995250949952Humanname
597797179CV3700908single nucleotide variantNM_012427.5(KLK5):c.152G>A (p.Gly51Glu)not specified [RCV004935719]uncertain significance195095003850950038Humanname
598221506CV3983843single nucleotide variantNM_012427.5(KLK5):c.226C>T (p.His76Tyr)not specified [RCV005360815]uncertain significance195094996450949964Humanname
156314949CV2253333single nucleotide variantNM_012427.5(KLK5):c.664C>T (p.Pro222Ser)not specified [RCV004123164]uncertain significance195094870250948702Humanname
155973689CV2317683single nucleotide variantNM_012427.5(KLK5):c.668G>A (p.Arg223Lys)not specified [RCV004174953]uncertain significance195094869850948698Humanname
156270483CV2326461single nucleotide variantNM_012427.5(KLK5):c.799G>T (p.Ala267Ser)not specified [RCV004183025]uncertain significance195094371450943714Humanname
156222451CV2343949single nucleotide variantNM_012427.5(KLK5):c.491G>A (p.Arg164His)not specified [RCV004195569]likely benign195094896050948960Humanname
156260310CV2359246single nucleotide variantNM_012427.5(KLK5):c.445G>A (p.Gly149Ser)not specified [RCV004212538]uncertain significance195094900650949006Humanname
156051895CV2363282single nucleotide variantNM_012427.5(KLK5):c.409G>T (p.Val137Phe)not specified [RCV004213835]uncertain significance195094904250949042Humanname
156148688CV2394510single nucleotide variantNM_012427.5(KLK5):c.814C>T (p.Pro272Ser)not specified [RCV004240868]uncertain significance195094369950943699Humanname
401722531CV2677019single nucleotide variantNM_012427.5(KLK5):c.665C>T (p.Pro222Leu)not specified [RCV004293620]uncertain significance195094870150948701Humanname
401866596CV2762693single nucleotide variantNM_012427.5(KLK5):c.803G>A (p.Arg268Gln)not specified [RCV004340254]likely benign195094371050943710Humanname
405814071CV3276418single nucleotide variantNM_012427.5(KLK5):c.421C>G (p.Pro141Ala)not specified [RCV004409654]uncertain significance195094903050949030Humanname
405814067CV3276420single nucleotide variantNM_012427.5(KLK5):c.481A>G (p.Arg161Gly)not specified [RCV004409656]uncertain significance195094897050948970Humanname
405814065CV3276421single nucleotide variantNM_012427.5(KLK5):c.580A>G (p.Lys194Glu)not specified [RCV004409657]uncertain significance195094887150948871Humanname
405814061CV3276423single nucleotide variantNM_012427.5(KLK5):c.623A>G (p.Asn208Ser)not specified [RCV004409659]uncertain significance195094874350948743Humanname
405814059CV3276424single nucleotide variantNM_012427.5(KLK5):c.652G>A (p.Glu218Lys)not specified [RCV004409660]likely benign195094871450948714Humanname
405814052CV3276427single nucleotide variantNM_012427.5(KLK5):c.677A>G (p.Asp226Gly)not specified [RCV004409663]uncertain significance195094868950948689Humanname
405814050CV3276428single nucleotide variantNM_012427.5(KLK5):c.736G>A (p.Gly246Arg)not specified [RCV004409664]uncertain significance195094377750943777Humanname
405813962CV3276430single nucleotide variantNM_012427.5(KLK5):c.802C>T (p.Arg268Trp)not specified [RCV004409666]uncertain significance195094371150943711Humanname
407499057CV3448684single nucleotide variantNM_012427.5(KLK5):c.443C>G (p.Pro148Arg)not specified [RCV004644215]uncertain significance195094900850949008Humanname
597797182CV3700909single nucleotide variantNM_012427.5(KLK5):c.355G>A (p.Gly119Ser)not specified [RCV004935720]uncertain significance195094909650949096Humanname
597797185CV3700910single nucleotide variantNM_012427.5(KLK5):c.756T>A (p.Asn252Lys)not specified [RCV004935721]uncertain significance195094375750943757Humanname