Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.93905792T>ACA78490854PROS1c.593A>T (p.Asp198Val)
c.556+37A>T (n.556+37A>T)
n.761A>T
c.551A>T (p.Asp184Val)
c.692A>T (n.692A>T)
c.689A>T (p.Asp230Val)
c.200A>T (p.Asp67Val)
 dbSNP COSMIC
3g.93905792T>CCA353673381PROS1c.593A>G (p.Asp198Gly)
c.556+37A>G (n.556+37A>G)
n.761A>G
c.551A>G (p.Asp184Gly)
c.692A>G (n.692A>G)
c.689A>G (p.Asp230Gly)
c.200A>G (p.Asp67Gly)
3g.93905792T>GCA353673382PROS1c.593A>C (p.Asp198Ala)
c.556+37A>C (n.556+37A>C)
n.761A>C
c.551A>C (p.Asp184Ala)
c.692A>C (n.692A>C)
c.689A>C (p.Asp230Ala)
c.200A>C (p.Asp67Ala)
3g.93905792T=CA1385042578PROS1c.593A= (p.Asp198=)
c.556+37A= (n.556+37A=)
n.761A=
c.551A= (p.Asp184=)
c.692A= (n.692A=)
c.689A= (p.Asp230=)
c.200A= (p.Asp67=)
3g.93905796_93905799delCA2666657497PROS1c.590_593del (p.Lys197IlefsTer10)
c.556+34_556+37del (n.556+34_556+37del)
n.758_761del
c.548_551del (p.Lys183IlefsTer10)
c.689_692del (n.689_692del)
c.686_689del (p.Lys229IlefsTer10)
c.686_689del (p.Lys229IlefsTer?)
c.197_200del (p.Lys66IlefsTer10)
 gnomAD v4
3g.93905793C>ACA353673383PROS1c.592G>T (p.Asp198Tyr)
c.556+36G>T (n.556+36G>T)
n.760G>T
c.550G>T (p.Asp184Tyr)
c.691G>T (n.691G>T)
c.688G>T (p.Asp230Tyr)
c.199G>T (p.Asp67Tyr)
 gnomAD v4 COSMIC
3g.93905793C>GCA353673384PROS1c.592G>C (p.Asp198His)
c.556+36G>C (n.556+36G>C)
n.760G>C
c.550G>C (p.Asp184His)
c.691G>C (n.691G>C)
c.688G>C (p.Asp230His)
c.199G>C (p.Asp67His)
 gnomAD v4
3g.93905793C>TCA353673385PROS1c.592G>A (p.Asp198Asn)
c.556+36G>A (n.556+36G>A)
n.760G>A
c.550G>A (p.Asp184Asn)
c.691G>A (n.691G>A)
c.688G>A (p.Asp230Asn)
c.199G>A (p.Asp67Asn)
3g.93905794T>ACA353673387PROS1c.591A>T (p.Lys197Asn)
c.556+35A>T (n.556+35A>T)
n.759A>T
c.549A>T (p.Lys183Asn)
c.690A>T (n.690A>T)
c.687A>T (p.Lys229Asn)
c.198A>T (p.Lys66Asn)
3g.93905794T>CCA434461748PROS1c.591A>G (p.Lys197=)
c.556+35A>G (n.556+35A>G)
n.759A>G
c.549A>G (p.Lys183=)
c.690A>G (n.690A>G)
c.687A>G (p.Lys229=)
c.198A>G (p.Lys66=)
 gnomAD v4
3g.93905794T>GCA353673386PROS1c.591A>C (p.Lys197Asn)
c.556+35A>C (n.556+35A>C)
n.759A>C
c.549A>C (p.Lys183Asn)
c.690A>C (n.690A>C)
c.687A>C (p.Lys229Asn)
c.198A>C (p.Lys66Asn)
3g.93905795T>ACA353673388PROS1c.590A>T (p.Lys197Ile)
c.556+34A>T (n.556+34A>T)
n.758A>T
c.548A>T (p.Lys183Ile)
c.689A>T (n.689A>T)
c.686A>T (p.Lys229Ile)
c.197A>T (p.Lys66Ile)
3g.93905795T>CCA78490861PROS1c.590A>G (p.Lys197Arg)
c.556+34A>G (n.556+34A>G)
n.758A>G
c.548A>G (p.Lys183Arg)
c.689A>G (n.689A>G)
c.686A>G (p.Lys229Arg)
c.197A>G (p.Lys66Arg)
 dbSNP gnomAD v3 gnomAD v4
3g.93905795T>GCA353673389PROS1c.590A>C (p.Lys197Thr)
c.556+34A>C (n.556+34A>C)
n.758A>C
c.548A>C (p.Lys183Thr)
c.689A>C (n.689A>C)
c.686A>C (p.Lys229Thr)
c.197A>C (p.Lys66Thr)
3g.93905795T=CA1385042579PROS1c.590A= (p.Lys197=)
c.556+34A= (n.556+34A=)
n.758A=
c.548A= (p.Lys183=)
c.689A= (n.689A=)
c.686A= (p.Lys229=)
c.197A= (p.Lys66=)
3g.93905796T>ACA353673390PROS1c.589A>T (p.Lys197Ter)
c.556+33A>T (n.556+33A>T)
n.757A>T
c.547A>T (p.Lys183Ter)
c.688A>T (n.688A>T)
c.685A>T (p.Lys229Ter)
c.196A>T (p.Lys66Ter)
3g.93905796T>CCA353673391PROS1c.589A>G (p.Lys197Glu)
c.556+33A>G (n.556+33A>G)
n.757A>G
c.547A>G (p.Lys183Glu)
c.688A>G (n.688A>G)
c.685A>G (p.Lys229Glu)
c.196A>G (p.Lys66Glu)
3g.93905796T>GCA353673392PROS1c.589A>C (p.Lys197Gln)
c.556+33A>C (n.556+33A>C)
n.757A>C
c.547A>C (p.Lys183Gln)
c.688A>C (n.688A>C)
c.685A>C (p.Lys229Gln)
c.196A>C (p.Lys66Gln)
3g.93905797C>ACA353673394PROS1c.588G>T (p.Lys196Asn)
c.556+32G>T (n.556+32G>T)
n.756G>T
c.546G>T (p.Lys182Asn)
c.687G>T (n.687G>T)
c.684G>T (p.Lys228Asn)
c.195G>T (p.Lys65Asn)
3g.93905797C=CA1385042580PROS1c.588G= (p.Lys196=)
c.556+32G= (n.556+32G=)
n.756G=
c.546G= (p.Lys182=)
c.687G= (n.687G=)
c.684G= (p.Lys228=)
c.195G= (p.Lys65=)
3g.93905797C>GCA353673393PROS1c.588G>C (p.Lys196Asn)
c.556+32G>C (n.556+32G>C)
n.756G>C
c.546G>C (p.Lys182Asn)
c.687G>C (n.687G>C)
c.684G>C (p.Lys228Asn)
c.195G>C (p.Lys65Asn)
3g.93905797C>TCA434626147PROS1c.588G>A (p.Lys196=)
c.556+32G>A (n.556+32G>A)
n.756G>A
c.546G>A (p.Lys182=)
c.687G>A (n.687G>A)
c.684G>A (p.Lys228=)
c.195G>A (p.Lys65=)
 dbSNP gnomAD v4
3g.93905798T>ACA353673395PROS1c.587A>T (p.Lys196Met)
c.556+31A>T (n.556+31A>T)
n.755A>T
c.545A>T (p.Lys182Met)
c.686A>T (n.686A>T)
c.683A>T (p.Lys228Met)
c.194A>T (p.Lys65Met)
3g.93905798T>CCA353673396PROS1c.587A>G (p.Lys196Arg)
c.556+31A>G (n.556+31A>G)
n.755A>G
c.545A>G (p.Lys182Arg)
c.686A>G (n.686A>G)
c.683A>G (p.Lys228Arg)
c.194A>G (p.Lys65Arg)
3g.93905798T>GCA353673397PROS1c.587A>C (p.Lys196Thr)
c.556+31A>C (n.556+31A>C)
n.755A>C
c.545A>C (p.Lys182Thr)
c.686A>C (n.686A>C)
c.683A>C (p.Lys228Thr)
c.194A>C (p.Lys65Thr)
3g.93905799T>ACA353673398PROS1c.586A>T (p.Lys196Ter)
c.556+30A>T (n.556+30A>T)
n.754A>T
c.544A>T (p.Lys182Ter)
c.685A>T (n.685A>T)
c.682A>T (p.Lys228Ter)
c.193A>T (p.Lys65Ter)
3g.93905799T>CCA123032PROS1c.586A>G (p.Lys196Glu)
c.556+30A>G (n.556+30A>G)
n.754A>G
c.544A>G (p.Lys182Glu)
c.685A>G (n.685A>G)
c.682A>G (p.Lys228Glu)
c.193A>G (p.Lys65Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905799T>GCA353673399PROS1c.586A>C (p.Lys196Gln)
c.556+30A>C (n.556+30A>C)
n.754A>C
c.544A>C (p.Lys182Gln)
c.685A>C (n.685A>C)
c.682A>C (p.Lys228Gln)
c.193A>C (p.Lys65Gln)
3g.93905799T=CA1385042581PROS1c.586A= (p.Lys196=)
c.556+30A= (n.556+30A=)
n.754A=
c.544A= (p.Lys182=)
c.685A= (n.685A=)
c.682A= (p.Lys228=)
c.193A= (p.Lys65=)
3g.93905800A=CA1385042582PROS1c.585T= (p.Asn195=)
c.556+29T= (n.556+29T=)
n.753T=
c.543T= (p.Asn181=)
c.684T= (n.684T=)
c.681T= (p.Asn227=)
c.192T= (p.Asn64=)
3g.93905800A>CCA353673400PROS1c.585T>G (p.Asn195Lys)
c.556+29T>G (n.556+29T>G)
n.753T>G
c.543T>G (p.Asn181Lys)
c.684T>G (n.684T>G)
c.681T>G (p.Asn227Lys)
c.192T>G (p.Asn64Lys)
3g.93905800A>GCA2503447PROS1c.585T>C (p.Asn195=)
c.556+29T>C (n.556+29T>C)
n.753T>C
c.543T>C (p.Asn181=)
c.684T>C (n.684T>C)
c.681T>C (p.Asn227=)
c.192T>C (p.Asn64=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905800A>TCA353673401PROS1c.585T>A (p.Asn195Lys)
c.556+29T>A (n.556+29T>A)
n.753T>A
c.543T>A (p.Asn181Lys)
c.684T>A (n.684T>A)
c.681T>A (p.Asn227Lys)
c.192T>A (p.Asn64Lys)
3g.93905801T>ACA353673402PROS1c.584A>T (p.Asn195Ile)
c.556+28A>T (n.556+28A>T)
n.752A>T
c.542A>T (p.Asn181Ile)
c.683A>T (n.683A>T)
c.680A>T (p.Asn227Ile)
c.191A>T (p.Asn64Ile)
3g.93905801T>CCA353673403PROS1c.584A>G (p.Asn195Ser)
c.556+28A>G (n.556+28A>G)
n.752A>G
c.542A>G (p.Asn181Ser)
c.683A>G (n.683A>G)
c.680A>G (p.Asn227Ser)
c.191A>G (p.Asn64Ser)
3g.93905801T>GCA353673404PROS1c.584A>C (p.Asn195Thr)
c.556+28A>C (n.556+28A>C)
n.752A>C
c.542A>C (p.Asn181Thr)
c.683A>C (n.683A>C)
c.680A>C (p.Asn227Thr)
c.191A>C (p.Asn64Thr)
3g.93905801_93905809delinsTTTGAAAGCCA1385042583PROS1c.576_584delinsGCTTTCAAA (p.Met192=)
c.556+20_556+28delinsGCTTTCAAA (n.556+20_556+28delinsGCTTTCAAA)
n.744_752delinsGCTTTCAAA
c.534_542delinsGCTTTCAAA (p.Met178=)
c.675_683delinsGCTTTCAAA (n.675_683delinsGCTTTCAAA)
c.672_680delinsGCTTTCAAA (p.Met224=)
c.183_191delinsGCTTTCAAA (p.Met61=)
3g.93905802T>ACA353673405PROS1c.583A>T (p.Asn195Tyr)
c.556+27A>T (n.556+27A>T)
n.751A>T
c.541A>T (p.Asn181Tyr)
c.682A>T (n.682A>T)
c.679A>T (p.Asn227Tyr)
c.190A>T (p.Asn64Tyr)
 dbSNP gnomAD v3 gnomAD v4
3g.93905802T>CCA353673406PROS1c.583A>G (p.Asn195Asp)
c.556+27A>G (n.556+27A>G)
n.751A>G
c.541A>G (p.Asn181Asp)
c.682A>G (n.682A>G)
c.679A>G (p.Asn227Asp)
c.190A>G (p.Asn64Asp)
 gnomAD v4
3g.93905802T>GCA353673407PROS1c.583A>C (p.Asn195His)
c.556+27A>C (n.556+27A>C)
n.751A>C
c.541A>C (p.Asn181His)
c.682A>C (n.682A>C)
c.679A>C (p.Asn227His)
c.190A>C (p.Asn64His)
3g.93905802T=CA1385042584PROS1c.583A= (p.Asn195=)
c.556+27A= (n.556+27A=)
n.751A=
c.541A= (p.Asn181=)
c.682A= (n.682A=)
c.679A= (p.Asn227=)
c.190A= (p.Asn64=)
3g.93905802_93905809delinsGCTTTCACA78490898PROS1c.576_583delinsTGAAAGC (p.Met192IlefsTer16)
c.556+20_556+27delinsTGAAAGC (n.556+20_556+27delinsTGAAAGC)
n.744_751delinsTGAAAGC
c.534_541delinsTGAAAGC (p.Met178IlefsTer16)
c.675_682delinsTGAAAGC (n.675_682delinsTGAAAGC)
c.672_679delinsTGAAAGC (p.Met224IlefsTer16)
c.672_679delinsTGAAAGC (p.Met224IlefsTer?)
c.183_190delinsTGAAAGC (p.Met61IlefsTer16)
 dbSNP
3g.93905803T>ACA434626153PROS1c.582A>T (p.Ser194=)
c.556+26A>T (n.556+26A>T)
n.750A>T
c.540A>T (p.Ser180=)
c.681A>T (n.681A>T)
c.678A>T (p.Ser226=)
c.189A>T (p.Ser63=)
3g.93905803T>CCA434626155PROS1c.582A>G (p.Ser194=)
c.556+26A>G (n.556+26A>G)
n.750A>G
c.540A>G (p.Ser180=)
c.681A>G (n.681A>G)
c.678A>G (p.Ser226=)
c.189A>G (p.Ser63=)
 dbSNP gnomAD v3 gnomAD v4
3g.93905803T>GCA434626157PROS1c.582A>C (p.Ser194=)
c.556+26A>C (n.556+26A>C)
n.750A>C
c.540A>C (p.Ser180=)
c.681A>C (n.681A>C)
c.678A>C (p.Ser226=)
c.189A>C (p.Ser63=)
 dbSNP gnomAD v2 gnomAD v4
3g.93905803T=CA1385042585PROS1c.582A= (p.Ser194=)
c.556+26A= (n.556+26A=)
n.750A=
c.540A= (p.Ser180=)
c.681A= (n.681A=)
c.678A= (p.Ser226=)
c.189A= (p.Ser63=)
3g.93905804G>ACA353673408PROS1c.581C>T (p.Ser194Leu)
c.556+25C>T (n.556+25C>T)
n.749C>T
c.539C>T (p.Ser180Leu)
c.680C>T (n.680C>T)
c.677C>T (p.Ser226Leu)
c.188C>T (p.Ser63Leu)
3g.93905804G>CCA353673409PROS1c.581C>G (p.Ser194Ter)
c.556+25C>G (n.556+25C>G)
n.749C>G
c.539C>G (p.Ser180Ter)
c.680C>G (n.680C>G)
c.677C>G (p.Ser226Ter)
c.188C>G (p.Ser63Ter)
 COSMIC
3g.93905804G=CA1385042586PROS1c.581C= (p.Ser194=)
c.556+25C= (n.556+25C=)
n.749C=
c.539C= (p.Ser180=)
c.680C= (n.680C=)
c.677C= (p.Ser226=)
c.188C= (p.Ser63=)
3g.93905804G>TCA353673410PROS1c.581C>A (p.Ser194Ter)
c.556+25C>A (n.556+25C>A)
n.749C>A
c.539C>A (p.Ser180Ter)
c.680C>A (n.680C>A)
c.677C>A (p.Ser226Ter)
c.188C>A (p.Ser63Ter)
 ClinVar dbSNP
3g.93905805A>CCA353673411PROS1c.580T>G (p.Ser194Ala)
c.556+24T>G (n.556+24T>G)
n.748T>G
c.538T>G (p.Ser180Ala)
c.679T>G (n.679T>G)
c.676T>G (p.Ser226Ala)
c.187T>G (p.Ser63Ala)
3g.93905805A>GCA353673412PROS1c.580T>C (p.Ser194Pro)
c.556+24T>C (n.556+24T>C)
n.748T>C
c.538T>C (p.Ser180Pro)
c.679T>C (n.679T>C)
c.676T>C (p.Ser226Pro)
c.187T>C (p.Ser63Pro)
3g.93905805A>TCA353673413PROS1c.580T>A (p.Ser194Thr)
c.556+24T>A (n.556+24T>A)
n.748T>A
c.538T>A (p.Ser180Thr)
c.679T>A (n.679T>A)
c.676T>A (p.Ser226Thr)
c.187T>A (p.Ser63Thr)
3g.93905807delCA2586972711PROS1c.580del (p.Ser194GlnfsTer14)
c.556+24del (n.556+24del)
n.748del
c.538del (p.Ser180GlnfsTer14)
c.679del (n.679del)
c.676del (p.Ser226GlnfsTer14)
c.676del (p.Ser226GlnfsTer?)
c.187del (p.Ser63GlnfsTer14)
3g.93905806A=CA1385042587PROS1c.579T= (p.Leu193=)
c.556+23T= (n.556+23T=)
n.747T=
c.537T= (p.Leu179=)
c.678T= (n.678T=)
c.675T= (p.Leu225=)
c.186T= (p.Leu62=)
3g.93905806A>CCA434626160PROS1c.579T>G (p.Leu193=)
c.556+23T>G (n.556+23T>G)
n.747T>G
c.537T>G (p.Leu179=)
c.678T>G (n.678T>G)
c.675T>G (p.Leu225=)
c.186T>G (p.Leu62=)
3g.93905806A>GCA2503448PROS1c.579T>C (p.Leu193=)
c.556+23T>C (n.556+23T>C)
n.747T>C
c.537T>C (p.Leu179=)
c.678T>C (n.678T>C)
c.675T>C (p.Leu225=)
c.186T>C (p.Leu62=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905806A>TCA434626163PROS1c.579T>A (p.Leu193=)
c.556+23T>A (n.556+23T>A)
n.747T>A
c.537T>A (p.Leu179=)
c.678T>A (n.678T>A)
c.675T>A (p.Leu225=)
c.186T>A (p.Leu62=)
3g.93905807A=CA1385042588PROS1c.578T= (p.Leu193=)
c.556+22T= (n.556+22T=)
n.746T=
c.536T= (p.Leu179=)
c.677T= (n.677T=)
c.674T= (p.Leu225=)
c.185T= (p.Leu62=)
3g.93905807A>CCA353673415PROS1c.578T>G (p.Leu193Arg)
c.556+22T>G (n.556+22T>G)
n.746T>G
c.536T>G (p.Leu179Arg)
c.677T>G (n.677T>G)
c.674T>G (p.Leu225Arg)
c.185T>G (p.Leu62Arg)
 gnomAD v3 gnomAD v4
3g.93905807A>GCA2503449PROS1c.578T>C (p.Leu193Pro)
c.556+22T>C (n.556+22T>C)
n.746T>C
c.536T>C (p.Leu179Pro)
c.677T>C (n.677T>C)
c.674T>C (p.Leu225Pro)
c.185T>C (p.Leu62Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.93905807A>TCA353673414PROS1c.578T>A (p.Leu193His)
c.556+22T>A (n.556+22T>A)
n.746T>A
c.536T>A (p.Leu179His)
c.677T>A (n.677T>A)
c.674T>A (p.Leu225His)
c.185T>A (p.Leu62His)
3g.93905808G>ACA353673416PROS1c.577C>T (p.Leu193Phe)
c.556+21C>T (n.556+21C>T)
n.745C>T
c.535C>T (p.Leu179Phe)
c.676C>T (n.676C>T)
c.673C>T (p.Leu225Phe)
c.184C>T (p.Leu62Phe)
 gnomAD v4
3g.93905808G>CCA353673417PROS1c.577C>G (p.Leu193Val)
c.556+21C>G (n.556+21C>G)
n.745C>G
c.535C>G (p.Leu179Val)
c.676C>G (n.676C>G)
c.673C>G (p.Leu225Val)
c.184C>G (p.Leu62Val)
3g.93905808G>TCA353673418PROS1c.577C>A (p.Leu193Ile)
c.556+21C>A (n.556+21C>A)
n.745C>A
c.535C>A (p.Leu179Ile)
c.676C>A (n.676C>A)
c.673C>A (p.Leu225Ile)
c.184C>A (p.Leu62Ile)
3g.93905809C>ACA353673419PROS1c.576G>T (p.Met192Ile)
c.556+20G>T (n.556+20G>T)
n.744G>T
c.534G>T (p.Met178Ile)
c.675G>T (n.675G>T)
c.672G>T (p.Met224Ile)
c.183G>T (p.Met61Ile)
3g.93905809C>GCA353673420PROS1c.576G>C (p.Met192Ile)
c.556+20G>C (n.556+20G>C)
n.744G>C
c.534G>C (p.Met178Ile)
c.675G>C (n.675G>C)
c.672G>C (p.Met224Ile)
c.183G>C (p.Met61Ile)
3g.93905809C>TCA353673421PROS1c.576G>A (p.Met192Ile)
c.556+20G>A (n.556+20G>A)
n.744G>A
c.534G>A (p.Met178Ile)
c.675G>A (n.675G>A)
c.672G>A (p.Met224Ile)
c.183G>A (p.Met61Ile)
3g.93905810A>CCA353673422PROS1c.575T>G (p.Met192Arg)
c.556+19T>G (n.556+19T>G)
n.743T>G
c.533T>G (p.Met178Arg)
c.674T>G (n.674T>G)
c.671T>G (p.Met224Arg)
c.182T>G (p.Met61Arg)
3g.93905810A>GCA353673423PROS1c.575T>C (p.Met192Thr)
c.556+19T>C (n.556+19T>C)
n.743T>C
c.533T>C (p.Met178Thr)
c.674T>C (n.674T>C)
c.671T>C (p.Met224Thr)
c.182T>C (p.Met61Thr)
3g.93905810A>TCA353673424PROS1c.575T>A (p.Met192Lys)
c.556+19T>A (n.556+19T>A)
n.743T>A
c.533T>A (p.Met178Lys)
c.674T>A (n.674T>A)
c.671T>A (p.Met224Lys)
c.182T>A (p.Met61Lys)
3g.93905811T>ACA353673425PROS1c.574A>T (p.Met192Leu)
c.556+18A>T (n.556+18A>T)
n.742A>T
c.532A>T (p.Met178Leu)
c.673A>T (n.673A>T)
c.670A>T (p.Met224Leu)
c.181A>T (p.Met61Leu)
 gnomAD v4
3g.93905811T>CCA353673426PROS1c.574A>G (p.Met192Val)
c.556+18A>G (n.556+18A>G)
n.742A>G
c.532A>G (p.Met178Val)
c.673A>G (n.673A>G)
c.670A>G (p.Met224Val)
c.181A>G (p.Met61Val)
 COSMIC
3g.93905811T>GCA353673427PROS1c.574A>C (p.Met192Leu)
c.556+18A>C (n.556+18A>C)
n.742A>C
c.532A>C (p.Met178Leu)
c.673A>C (n.673A>C)
c.670A>C (p.Met224Leu)
c.181A>C (p.Met61Leu)
3g.93905812A>CCA434626169PROS1c.573T>G (p.Val191=)
c.556+17T>G (n.556+17T>G)
n.741T>G
c.531T>G (p.Val177=)
c.672T>G (n.672T>G)
c.669T>G (p.Val223=)
c.180T>G (p.Val60=)
3g.93905812A>GCA434626172PROS1c.573T>C (p.Val191=)
c.556+17T>C (n.556+17T>C)
n.741T>C
c.531T>C (p.Val177=)
c.672T>C (n.672T>C)
c.669T>C (p.Val223=)
c.180T>C (p.Val60=)
3g.93905812A>TCA434626171PROS1c.573T>A (p.Val191=)
c.556+17T>A (n.556+17T>A)
n.741T>A
c.531T>A (p.Val177=)
c.672T>A (n.672T>A)
c.669T>A (p.Val223=)
c.180T>A (p.Val60=)
 ClinVar
3g.93905813A=CA1385042589PROS1c.572T= (p.Val191=)
c.556+16T= (n.556+16T=)
n.740T=
c.530T= (p.Val177=)
c.671T= (n.671T=)
c.668T= (p.Val223=)
c.179T= (p.Val60=)
3g.93905813A>CCA353673428PROS1c.572T>G (p.Val191Gly)
c.556+16T>G (n.556+16T>G)
n.740T>G
c.530T>G (p.Val177Gly)
c.671T>G (n.671T>G)
c.668T>G (p.Val223Gly)
c.179T>G (p.Val60Gly)
3g.93905813A>GCA353673429PROS1c.572T>C (p.Val191Ala)
c.556+16T>C (n.556+16T>C)
n.740T>C
c.530T>C (p.Val177Ala)
c.671T>C (n.671T>C)
c.668T>C (p.Val223Ala)
c.179T>C (p.Val60Ala)
3g.93905813A>TCA2503450PROS1c.572T>A (p.Val191Asp)
c.556+16T>A (n.556+16T>A)
n.740T>A
c.530T>A (p.Val177Asp)
c.671T>A (n.671T>A)
c.668T>A (p.Val223Asp)
c.179T>A (p.Val60Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.93905814C>ACA353673430PROS1c.571G>T (p.Val191Phe)
c.556+15G>T (n.556+15G>T)
n.739G>T
c.529G>T (p.Val177Phe)
c.670G>T (n.670G>T)
c.667G>T (p.Val223Phe)
c.178G>T (p.Val60Phe)
3g.93905814C=CA1385042590PROS1c.571G= (p.Val191=)
c.556+15G= (n.556+15G=)
n.739G=
c.529G= (p.Val177=)
c.670G= (n.670G=)
c.667G= (p.Val223=)
c.178G= (p.Val60=)
3g.93905814C>GCA353673432PROS1c.571G>C (p.Val191Leu)
c.556+15G>C (n.556+15G>C)
n.739G>C
c.529G>C (p.Val177Leu)
c.670G>C (n.670G>C)
c.667G>C (p.Val223Leu)
c.178G>C (p.Val60Leu)
 dbSNP gnomAD v3 gnomAD v4
3g.93905814C>TCA353673431PROS1c.571G>A (p.Val191Ile)
c.556+15G>A (n.556+15G>A)
n.739G>A
c.529G>A (p.Val177Ile)
c.670G>A (n.670G>A)
c.667G>A (p.Val223Ile)
c.178G>A (p.Val60Ile)
 dbSNP COSMIC
3g.93905815A>CCA353673433PROS1c.570T>G (p.Phe190Leu)
c.556+14T>G (n.556+14T>G)
n.738T>G
c.528T>G (p.Phe176Leu)
c.669T>G (n.669T>G)
c.666T>G (p.Phe222Leu)
c.177T>G (p.Phe59Leu)
3g.93905815A>GCA434626179PROS1c.570T>C (p.Phe190=)
c.556+14T>C (n.556+14T>C)
n.738T>C
c.528T>C (p.Phe176=)
c.669T>C (n.669T>C)
c.666T>C (p.Phe222=)
c.177T>C (p.Phe59=)
3g.93905815A>TCA353673434PROS1c.570T>A (p.Phe190Leu)
c.556+14T>A (n.556+14T>A)
n.738T>A
c.528T>A (p.Phe176Leu)
c.669T>A (n.669T>A)
c.666T>A (p.Phe222Leu)
c.177T>A (p.Phe59Leu)
3g.93905816A>CCA353673435PROS1c.569T>G (p.Phe190Cys)
c.556+13T>G (n.556+13T>G)
n.737T>G
c.527T>G (p.Phe176Cys)
c.668T>G (n.668T>G)
c.665T>G (p.Phe222Cys)
c.176T>G (p.Phe59Cys)
3g.93905816A>GCA353673436PROS1c.569T>C (p.Phe190Ser)
c.556+13T>C (n.556+13T>C)
n.737T>C
c.527T>C (p.Phe176Ser)
c.668T>C (n.668T>C)
c.665T>C (p.Phe222Ser)
c.176T>C (p.Phe59Ser)
3g.93905816A>TCA353673437PROS1c.569T>A (p.Phe190Tyr)
c.556+13T>A (n.556+13T>A)
n.737T>A
c.527T>A (p.Phe176Tyr)
c.668T>A (n.668T>A)
c.665T>A (p.Phe222Tyr)
c.176T>A (p.Phe59Tyr)
3g.93905817A>CCA353673438PROS1c.568T>G (p.Phe190Val)
c.556+12T>G (n.556+12T>G)
n.736T>G
c.526T>G (p.Phe176Val)
c.667T>G (n.667T>G)
c.664T>G (p.Phe222Val)
c.175T>G (p.Phe59Val)
3g.93905817A>GCA353673439PROS1c.568T>C (p.Phe190Leu)
c.556+12T>C (n.556+12T>C)
n.736T>C
c.526T>C (p.Phe176Leu)
c.667T>C (n.667T>C)
c.664T>C (p.Phe222Leu)
c.175T>C (p.Phe59Leu)
 gnomAD v4
3g.93905817A>TCA353673440PROS1c.568T>A (p.Phe190Ile)
c.556+12T>A (n.556+12T>A)
n.736T>A
c.526T>A (p.Phe176Ile)
c.667T>A (n.667T>A)
c.664T>A (p.Phe222Ile)
c.175T>A (p.Phe59Ile)
3g.93905818A>CCA434626184PROS1c.567T>G (p.Gly189=)
c.556+11T>G (n.556+11T>G)
n.735T>G
c.525T>G (p.Gly175=)
c.666T>G (n.666T>G)
c.663T>G (p.Gly221=)
c.174T>G (p.Gly58=)
3g.93905818A>GCA434626185PROS1c.567T>C (p.Gly189=)
c.556+11T>C (n.556+11T>C)
n.735T>C
c.525T>C (p.Gly175=)
c.666T>C (n.666T>C)
c.663T>C (p.Gly221=)
c.174T>C (p.Gly58=)
 gnomAD v4
3g.93905818A>TCA434626186PROS1c.567T>A (p.Gly189=)
c.556+11T>A (n.556+11T>A)
n.735T>A
c.525T>A (p.Gly175=)
c.666T>A (n.666T>A)
c.663T>A (p.Gly221=)
c.174T>A (p.Gly58=)
3g.93905819C>ACA353673441PROS1c.566G>T (p.Gly189Val)
c.556+10G>T (n.556+10G>T)
n.734G>T
c.524G>T (p.Gly175Val)
c.665G>T (n.665G>T)
c.662G>T (p.Gly221Val)
c.173G>T (p.Gly58Val)
3g.93905819C=CA1385042591PROS1c.566G= (p.Gly189=)
c.556+10G= (n.556+10G=)
n.734G=
c.524G= (p.Gly175=)
c.665G= (n.665G=)
c.662G= (p.Gly221=)
c.173G= (p.Gly58=)
3g.93905819C>GCA353673442PROS1c.566G>C (p.Gly189Ala)
c.556+10G>C (n.556+10G>C)
n.734G>C
c.524G>C (p.Gly175Ala)
c.665G>C (n.665G>C)
c.662G>C (p.Gly221Ala)
c.173G>C (p.Gly58Ala)
 gnomAD v4
3g.93905819C>TCA353673443PROS1c.566G>A (p.Gly189Asp)
c.556+10G>A (n.556+10G>A)
n.734G>A
c.524G>A (p.Gly175Asp)
c.665G>A (n.665G>A)
c.662G>A (p.Gly221Asp)
c.173G>A (p.Gly58Asp)
 ClinVar dbSNP
3g.93905820C>ACA353673446PROS1c.565G>T (p.Gly189Cys)
c.556+9G>T (n.556+9G>T)
n.733G>T
c.523G>T (p.Gly175Cys)
c.664G>T (n.664G>T)
c.661G>T (p.Gly221Cys)
c.172G>T (p.Gly58Cys)
3g.93905820C>GCA353673444PROS1c.565G>C (p.Gly189Arg)
c.556+9G>C (n.556+9G>C)
n.733G>C
c.523G>C (p.Gly175Arg)
c.664G>C (n.664G>C)
c.661G>C (p.Gly221Arg)
c.172G>C (p.Gly58Arg)
3g.93905820C>TCA353673445PROS1c.565G>A (p.Gly189Ser)
c.556+9G>A (n.556+9G>A)
n.733G>A
c.523G>A (p.Gly175Ser)
c.664G>A (n.664G>A)
c.661G>A (p.Gly221Ser)
c.172G>A (p.Gly58Ser)
3g.93905821A=CA1385042593PROS1c.564T= (p.Asn188=)
c.556+8T= (n.556+8T=)
c.171T= (p.Asn57=)
n.732T=
c.522T= (p.Asn174=)
c.663T= (n.663T=)
c.660T= (p.Asn220=)
3g.93905821A>CCA353673447PROS1c.564T>G (p.Asn188Lys)
c.556+8T>G (n.556+8T>G)
c.171T>G (p.Asn57Lys)
n.732T>G
c.522T>G (p.Asn174Lys)
c.663T>G (n.663T>G)
c.660T>G (p.Asn220Lys)
3g.93905821A>GCA434626192PROS1c.564T>C (p.Asn188=)
c.556+8T>C (n.556+8T>C)
c.171T>C (p.Asn57=)
n.732T>C
c.522T>C (p.Asn174=)
c.663T>C (n.663T>C)
c.660T>C (p.Asn220=)
 dbSNP
3g.93905821A>TCA353673448PROS1c.564T>A (p.Asn188Lys)
c.556+8T>A (n.556+8T>A)
c.171T>A (p.Asn57Lys)
n.732T>A
c.522T>A (p.Asn174Lys)
c.663T>A (n.663T>A)
c.660T>A (p.Asn220Lys)
3g.93905821_93905822delinsATCA1385042592PROS1c.563_564delinsAT (p.Asn188=)
c.556+7_556+8delinsAT (n.556+7_556+8delinsAT)
c.170_171delinsAT (p.Asn57=)
n.731_732delinsAT
c.521_522delinsAT (p.Asn174=)
c.662_663delinsAT (n.662_663delinsAT)
c.659_660delinsAT (p.Asn220=)
3g.93905822T>ACA353673449PROS1c.563A>T (p.Asn188Ile)
c.556+7A>T (n.556+7A>T)
c.170A>T (p.Asn57Ile)
n.731A>T
c.521A>T (p.Asn174Ile)
c.662A>T (n.662A>T)
c.659A>T (p.Asn220Ile)
3g.93905822T>CCA2503452PROS1c.563A>G (p.Asn188Ser)
c.556+7A>G (n.556+7A>G)
c.170A>G (p.Asn57Ser)
n.731A>G
c.521A>G (p.Asn174Ser)
c.662A>G (n.662A>G)
c.659A>G (p.Asn220Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905822T>GCA353673450PROS1c.563A>C (p.Asn188Thr)
c.556+7A>C (n.556+7A>C)
c.170A>C (p.Asn57Thr)
n.731A>C
c.521A>C (p.Asn174Thr)
c.662A>C (n.662A>C)
c.659A>C (p.Asn220Thr)
3g.93905822T=CA1385042594PROS1c.563A= (p.Asn188=)
c.556+7A= (n.556+7A=)
c.170A= (p.Asn57=)
n.731A=
c.521A= (p.Asn174=)
c.662A= (n.662A=)
c.659A= (p.Asn220=)
3g.93905826dupCA915940538PROS1c.563dup (p.Asn188LysfsTer9)
c.556+7dup (n.556+7dup)
c.170dup (p.Asn57LysfsTer?)
n.731dup
c.521dup (p.Asn174LysfsTer9)
c.662dup (n.662dup)
c.659dup (p.Asn220LysfsTer9)
c.170dup (p.Asn57LysfsTer9)
3g.93905826delCA2503451PROS1c.563del (p.Asn188MetfsTer20)
c.556+7del (n.556+7del)
c.170del (p.Asn57=)
n.731del
c.521del (p.Asn174MetfsTer20)
c.662del (n.662del)
c.659del (p.Asn220MetfsTer20)
c.659del (p.Asn220MetfsTer?)
c.170del (p.Asn57MetfsTer20)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.93905823T>ACA353673451PROS1c.562A>T (p.Asn188Tyr)
c.556+6A>T (n.556+6A>T)
c.169A>T (p.Asn57Tyr)
n.730A>T
c.520A>T (p.Asn174Tyr)
c.661A>T (n.661A>T)
c.658A>T (p.Asn220Tyr)
3g.93905823T>CCA353673452PROS1c.562A>G (p.Asn188Asp)
c.556+6A>G (n.556+6A>G)
c.169A>G (p.Asn57Asp)
n.730A>G
c.520A>G (p.Asn174Asp)
c.661A>G (n.661A>G)
c.658A>G (p.Asn220Asp)
3g.93905823T>GCA353673453PROS1c.562A>C (p.Asn188His)
c.556+6A>C (n.556+6A>C)
c.169A>C (p.Asn57His)
n.730A>C
c.520A>C (p.Asn174His)
c.661A>C (n.661A>C)
c.658A>C (p.Asn220His)
3g.93905824T>ACA353673454PROS1c.561A>T (p.Lys187Asn)
c.556+5A>T (n.556+5A>T)
c.168A>T (p.Lys56Asn)
n.729A>T
c.519A>T (p.Lys173Asn)
c.660A>T (n.660A>T)
c.657A>T (p.Lys219Asn)
3g.93905824T>CCA434626199PROS1c.561A>G (p.Lys187=)
c.556+5A>G (n.556+5A>G)
c.168A>G (p.Lys56=)
n.729A>G
c.519A>G (p.Lys173=)
c.660A>G (n.660A>G)
c.657A>G (p.Lys219=)
3g.93905824T>GCA353673455PROS1c.561A>C (p.Lys187Asn)
c.556+5A>C (n.556+5A>C)
c.168A>C (p.Lys56Asn)
n.729A>C
c.519A>C (p.Lys173Asn)
c.660A>C (n.660A>C)
c.657A>C (p.Lys219Asn)
3g.93905825T>ACA353673457PROS1c.560A>T (p.Lys187Ile)
c.556+4A>T (n.556+4A>T)
c.167A>T (p.Lys56Ile)
n.728A>T
c.518A>T (p.Lys173Ile)
c.659A>T (n.659A>T)
c.656A>T (p.Lys219Ile)
3g.93905825T>CCA78490916PROS1c.560A>G (p.Lys187Arg)
c.556+4A>G (n.556+4A>G)
c.167A>G (p.Lys56Arg)
n.728A>G
c.518A>G (p.Lys173Arg)
c.659A>G (n.659A>G)
c.656A>G (p.Lys219Arg)
 dbSNP
3g.93905825T>GCA353673456PROS1c.560A>C (p.Lys187Thr)
c.556+4A>C (n.556+4A>C)
c.167A>C (p.Lys56Thr)
n.728A>C
c.518A>C (p.Lys173Thr)
c.659A>C (n.659A>C)
c.656A>C (p.Lys219Thr)
3g.93905825T=CA1385042595PROS1c.560A= (p.Lys187=)
c.556+4A= (n.556+4A=)
c.167A= (p.Lys56=)
n.728A=
c.518A= (p.Lys173=)
c.659A= (n.659A=)
c.656A= (p.Lys219=)
3g.93905826T>ACA353673458PROS1c.559A>T (p.Lys187Ter)
c.556+3A>T (n.556+3A>T)
c.166A>T (p.Lys56Ter)
n.727A>T
c.517A>T (p.Lys173Ter)
c.658A>T (n.658A>T)
c.655A>T (p.Lys219Ter)
3g.93905826T>CCA353673459PROS1c.559A>G (p.Lys187Glu)
c.556+3A>G (n.556+3A>G)
c.166A>G (p.Lys56Glu)
n.727A>G
c.517A>G (p.Lys173Glu)
c.658A>G (n.658A>G)
c.655A>G (p.Lys219Glu)
3g.93905826T>GCA353673460PROS1c.559A>C (p.Lys187Gln)
c.556+3A>C (n.556+3A>C)
c.166A>C (p.Lys56Gln)
n.727A>C
c.517A>C (p.Lys173Gln)
c.658A>C (n.658A>C)
c.655A>C (p.Lys219Gln)
3g.93905827A>CCA353673461PROS1c.558T>G (p.Cys186Trp)
c.556+2T>G (n.556+2T>G)
c.165T>G (p.Cys55Trp)
n.726T>G
c.516T>G (p.Cys172Trp)
c.657T>G (n.657T>G)
c.654T>G (p.Cys218Trp)
3g.93905827A>GCA434626206PROS1c.558T>C (p.Cys186=)
c.556+2T>C (n.556+2T>C)
c.165T>C (p.Cys55=)
n.726T>C
c.516T>C (p.Cys172=)
c.657T>C (n.657T>C)
c.654T>C (p.Cys218=)
3g.93905827A>TCA353673462PROS1c.558T>A (p.Cys186Ter)
c.556+2T>A (n.556+2T>A)
c.165T>A (p.Cys55Ter)
n.726T>A
c.516T>A (p.Cys172Ter)
c.657T>A (n.657T>A)
c.654T>A (p.Cys218Ter)
3g.93905828C>ACA353673463PROS1c.557G>T (p.Cys186Phe)
c.556+1G>T (n.556+1G>T)
c.164G>T (p.Cys55Phe)
n.725G>T
c.515G>T (p.Cys172Phe)
c.656G>T (n.656G>T)
c.653G>T (p.Cys218Phe)
3g.93905828C=CA1385042596PROS1c.557G= (p.Cys186=)
c.556+1G= (n.556+1G=)
c.164G= (p.Cys55=)
n.725G=
c.515G= (p.Cys172=)
c.656G= (n.656G=)
c.653G= (p.Cys218=)
3g.93905828C>GCA353673464PROS1c.557G>C (p.Cys186Ser)
c.556+1G>C (n.556+1G>C)
c.164G>C (p.Cys55Ser)
n.725G>C
c.515G>C (p.Cys172Ser)
c.656G>C (n.656G>C)
c.653G>C (p.Cys218Ser)
 dbSNP gnomAD v3 gnomAD v4
3g.93905828C>TCA2503453PROS1c.557G>A (p.Cys186Tyr)
c.556+1G>A (n.556+1G>A)
c.164G>A (p.Cys55Tyr)
n.725G>A
c.515G>A (p.Cys172Tyr)
c.656G>A (n.656G>A)
c.653G>A (p.Cys218Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.93905829A>CCA353673465PROS1c.556T>G (p.Cys186Gly)
c.556T>G (p.Tyr186Asp)
c.163T>G (p.Cys55Gly)
n.724T>G
c.514T>G (p.Cys172Gly)
c.655T>G (n.655T>G)
c.652T>G (p.Cys218Gly)
3g.93905829A>GCA353673466PROS1c.556T>C (p.Cys186Arg)
c.556T>C (p.Tyr186His)
c.163T>C (p.Cys55Arg)
n.724T>C
c.514T>C (p.Cys172Arg)
c.655T>C (n.655T>C)
c.652T>C (p.Cys218Arg)
3g.93905829A>TCA353673467PROS1c.556T>A (p.Cys186Ser)
c.556T>A (p.Tyr186Asn)
c.163T>A (p.Cys55Ser)
n.724T>A
c.514T>A (p.Cys172Ser)
c.655T>A (n.655T>A)
c.652T>A (p.Cys218Ser)
3g.93905830G>ACA2503454PROS1c.555C>T (p.Ser185=)
c.162C>T (p.Ser54=)
n.723C>T
c.513C>T (p.Ser171=)
c.654C>T (n.654C>T)
c.651C>T (p.Ser217=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.93905830G>CCA434626211PROS1c.555C>G (p.Ser185=)
c.162C>G (p.Ser54=)
n.723C>G
c.513C>G (p.Ser171=)
c.654C>G (n.654C>G)
c.651C>G (p.Ser217=)
3g.93905830G=CA1385042597PROS1c.555C= (p.Ser185=)
c.162C= (p.Ser54=)
n.723C=
c.513C= (p.Ser171=)
c.654C= (n.654C=)
c.651C= (p.Ser217=)
3g.93905830G>TCA434626213PROS1c.555C>A (p.Ser185=)
c.162C>A (p.Ser54=)
n.723C>A
c.513C>A (p.Ser171=)
c.654C>A (n.654C>A)
c.651C>A (p.Ser217=)
3g.93905831G>ACA78490921PROS1c.554C>T (p.Ser185Phe)
c.161C>T (p.Ser54Phe)
n.722C>T
c.512C>T (p.Ser171Phe)
c.653C>T (n.653C>T)
c.650C>T (p.Ser217Phe)
 dbSNP
3g.93905831G>CCA353673469PROS1c.554C>G (p.Ser185Cys)
c.161C>G (p.Ser54Cys)
n.722C>G
c.512C>G (p.Ser171Cys)
c.653C>G (n.653C>G)
c.650C>G (p.Ser217Cys)
 gnomAD v4
3g.93905831G=CA1385042598PROS1c.554C= (p.Ser185=)
c.161C= (p.Ser54=)
n.722C=
c.512C= (p.Ser171=)
c.653C= (n.653C=)
c.650C= (p.Ser217=)
3g.93905831G>TCA353673468PROS1c.554C>A (p.Ser185Tyr)
c.161C>A (p.Ser54Tyr)
n.722C>A
c.512C>A (p.Ser171Tyr)
c.653C>A (n.653C>A)
c.650C>A (p.Ser217Tyr)
3g.93905832A>CCA353673470PROS1c.553T>G (p.Ser185Ala)
c.160T>G (p.Ser54Ala)
n.721T>G
c.511T>G (p.Ser171Ala)
c.652T>G (n.652T>G)
c.649T>G (p.Ser217Ala)
3g.93905832A>GCA353673471PROS1c.553T>C (p.Ser185Pro)
c.160T>C (p.Ser54Pro)
n.721T>C
c.511T>C (p.Ser171Pro)
c.652T>C (n.652T>C)
c.649T>C (p.Ser217Pro)
3g.93905832A>TCA353673472PROS1c.553T>A (p.Ser185Thr)
c.160T>A (p.Ser54Thr)
n.721T>A
c.511T>A (p.Ser171Thr)
c.652T>A (n.652T>A)
c.649T>A (p.Ser217Thr)
3g.93905833A>CCA353673473PROS1c.552T>G (p.Cys184Trp)
c.159T>G (p.Cys53Trp)
n.720T>G
c.510T>G (p.Cys170Trp)
c.651T>G (n.651T>G)
c.648T>G (p.Cys216Trp)
3g.93905833A>GCA434626216PROS1c.552T>C (p.Cys184=)
c.159T>C (p.Cys53=)
n.720T>C
c.510T>C (p.Cys170=)
c.651T>C (n.651T>C)
c.648T>C (p.Cys216=)
3g.93905833A>TCA353673474PROS1c.552T>A (p.Cys184Ter)
c.159T>A (p.Cys53Ter)
n.720T>A
c.510T>A (p.Cys170Ter)
c.651T>A (n.651T>A)
c.648T>A (p.Cys216Ter)
3g.93905834C>ACA353673477PROS1c.551G>T (p.Cys184Phe)
c.158G>T (p.Cys53Phe)
n.719G>T
c.509G>T (p.Cys170Phe)
c.650G>T (n.650G>T)
c.647G>T (p.Cys216Phe)
3g.93905834C>GCA353673475PROS1c.551G>C (p.Cys184Ser)
c.158G>C (p.Cys53Ser)
n.719G>C
c.509G>C (p.Cys170Ser)
c.650G>C (n.650G>C)
c.647G>C (p.Cys216Ser)
3g.93905834C>TCA353673476PROS1c.551G>A (p.Cys184Tyr)
c.158G>A (p.Cys53Tyr)
n.719G>A
c.509G>A (p.Cys170Tyr)
c.650G>A (n.650G>A)
c.647G>A (p.Cys216Tyr)
 gnomAD v4
3g.93905834_93905835delinsCACA1385042599PROS1c.550_551delinsTG (p.Cys184=)
c.157_158delinsTG (p.Cys53=)
n.718_719delinsTG
c.508_509delinsTG (p.Cys170=)
c.649_650delinsTG (n.649_650delinsTG)
c.646_647delinsTG (p.Cys216=)
3g.93905835delCA915941517PROS1c.550del (p.Cys184ValfsTer24)
c.550del (p.Cys184ValfsTer9)
c.157del (p.Cys53ValfsTer?)
n.718del
c.508del (p.Cys170ValfsTer24)
c.649del (n.649del)
c.646del (p.Cys216ValfsTer24)
c.646del (p.Cys216ValfsTer?)
c.157del (p.Cys53ValfsTer24)
 ClinVar dbSNP
3g.93905835A>CCA353673478PROS1c.550T>G (p.Cys184Gly)
c.157T>G (p.Cys53Gly)
n.718T>G
c.508T>G (p.Cys170Gly)
c.649T>G (n.649T>G)
c.646T>G (p.Cys216Gly)
3g.93905835A>GCA353673479PROS1c.550T>C (p.Cys184Arg)
c.157T>C (p.Cys53Arg)
n.718T>C
c.508T>C (p.Cys170Arg)
c.649T>C (n.649T>C)
c.646T>C (p.Cys216Arg)
3g.93905835A>TCA353673480PROS1c.550T>A (p.Cys184Ser)
c.157T>A (p.Cys53Ser)
n.718T>A
c.508T>A (p.Cys170Ser)
c.649T>A (n.649T>A)
c.646T>A (p.Cys216Ser)
 gnomAD v4
3g.93905836G>ACA434626218PROS1c.549C>T (p.His183=)
c.156C>T (p.His52=)
n.717C>T
c.507C>T (p.His169=)
c.648C>T (n.648C>T)
c.645C>T (p.His215=)
3g.93905836G>CCA353673481PROS1c.549C>G (p.His183Gln)
c.156C>G (p.His52Gln)
n.717C>G
c.507C>G (p.His169Gln)
c.648C>G (n.648C>G)
c.645C>G (p.His215Gln)
3g.93905836G=CA1385042600PROS1c.549C= (p.His183=)
c.156C= (p.His52=)
n.717C=
c.507C= (p.His169=)
c.648C= (n.648C=)
c.645C= (p.His215=)
3g.93905836G>TCA353673482PROS1c.549C>A (p.His183Gln)
c.156C>A (p.His52Gln)
n.717C>A
c.507C>A (p.His169Gln)
c.648C>A (n.648C>A)
c.645C>A (p.His215Gln)
 dbSNP
3g.93905837T>ACA353673485PROS1c.548A>T (p.His183Leu)
c.155A>T (p.His52Leu)
n.716A>T
c.506A>T (p.His169Leu)
c.647A>T (n.647A>T)
c.644A>T (p.His215Leu)
3g.93905837T>CCA353673484PROS1c.548A>G (p.His183Arg)
c.155A>G (p.His52Arg)
n.716A>G
c.506A>G (p.His169Arg)
c.647A>G (n.647A>G)
c.644A>G (p.His215Arg)
 dbSNP gnomAD v2
3g.93905837T>GCA353673483PROS1c.548A>C (p.His183Pro)
c.155A>C (p.His52Pro)
n.716A>C
c.506A>C (p.His169Pro)
c.647A>C (n.647A>C)
c.644A>C (p.His215Pro)
3g.93905837T=CA1385042601PROS1c.548A= (p.His183=)
c.155A= (p.His52=)
n.716A=
c.506A= (p.His169=)
c.647A= (n.647A=)
c.644A= (p.His215=)
3g.93905837_93905838delinsTGCA1385042602PROS1c.547_548delinsCA (p.His183=)
c.154_155delinsCA (p.His52=)
n.715_716delinsCA
c.505_506delinsCA (p.His169=)
c.646_647delinsCA (n.646_647delinsCA)
c.643_644delinsCA (p.His215=)
3g.93905838G>ACA353673486PROS1c.547C>T (p.His183Tyr)
c.154C>T (p.His52Tyr)
n.715C>T
c.505C>T (p.His169Tyr)
c.646C>T (n.646C>T)
c.643C>T (p.His215Tyr)
 gnomAD v4
3g.93905838G>CCA353673488PROS1c.547C>G (p.His183Asp)
c.154C>G (p.His52Asp)
n.715C>G
c.505C>G (p.His169Asp)
c.646C>G (n.646C>G)
c.643C>G (p.His215Asp)
3g.93905838G>TCA353673487PROS1c.547C>A (p.His183Asn)
c.154C>A (p.His52Asn)
n.715C>A
c.505C>A (p.His169Asn)
c.646C>A (n.646C>A)
c.643C>A (p.His215Asn)
 gnomAD v4
3g.93905839delCA545016845PROS1c.547del (p.His183ThrfsTer25)
c.547del (p.His183ThrfsTer10)
c.154del (p.His52ThrfsTer?)
n.715del
c.505del (p.His169ThrfsTer25)
c.646del (n.646del)
c.643del (p.His215ThrfsTer25)
c.643del (p.His215ThrfsTer?)
c.154del (p.His52ThrfsTer25)
 dbSNP gnomAD v2 gnomAD v4
3g.93905839G>ACA434626220PROS1c.546C>T (p.Tyr182=)
c.153C>T (p.Tyr51=)
n.714C>T
c.504C>T (p.Tyr168=)
c.645C>T (n.645C>T)
c.642C>T (p.Tyr214=)
 gnomAD v4
3g.93905839G>CCA353673489PROS1c.546C>G (p.Tyr182Ter)
c.153C>G (p.Tyr51Ter)
n.714C>G
c.504C>G (p.Tyr168Ter)
c.645C>G (n.645C>G)
c.642C>G (p.Tyr214Ter)
3g.93905839G>TCA353673490PROS1c.546C>A (p.Tyr182Ter)
c.153C>A (p.Tyr51Ter)
n.714C>A
c.504C>A (p.Tyr168Ter)
c.645C>A (n.645C>A)
c.642C>A (p.Tyr214Ter)
3g.93905840delCA2586972712PROS1c.545del (p.Tyr182SerfsTer26)
c.545del (p.Tyr182SerfsTer11)
c.152del (p.Tyr51SerfsTer?)
n.713del
c.503del (p.Tyr168SerfsTer26)
c.644del (n.644del)
c.641del (p.Tyr214SerfsTer26)
c.641del (p.Tyr214SerfsTer?)
c.152del (p.Tyr51SerfsTer26)
3g.93905840T>ACA353673491PROS1c.545A>T (p.Tyr182Phe)
c.152A>T (p.Tyr51Phe)
n.713A>T
c.503A>T (p.Tyr168Phe)
c.644A>T (n.644A>T)
c.641A>T (p.Tyr214Phe)
3g.93905840T>CCA353673492PROS1c.545A>G (p.Tyr182Cys)
c.152A>G (p.Tyr51Cys)
n.713A>G
c.503A>G (p.Tyr168Cys)
c.644A>G (n.644A>G)
c.641A>G (p.Tyr214Cys)
 gnomAD v4
3g.93905840T>GCA353673493PROS1c.545A>C (p.Tyr182Ser)
c.152A>C (p.Tyr51Ser)
n.713A>C
c.503A>C (p.Tyr168Ser)
c.644A>C (n.644A>C)
c.641A>C (p.Tyr214Ser)
3g.93905840dupCA2586972713PROS1c.545dup (p.Tyr182Ter)
c.152dup (p.Tyr51Ter)
n.713dup
c.503dup (p.Tyr168Ter)
c.644dup (n.644dup)
c.641dup (p.Tyr214Ter)
3g.93905841A>CCA353673494PROS1c.544T>G (p.Tyr182Asp)
c.151T>G (p.Tyr51Asp)
n.712T>G
c.502T>G (p.Tyr168Asp)
c.643T>G (n.643T>G)
c.640T>G (p.Tyr214Asp)
3g.93905841A>GCA353673495PROS1c.544T>C (p.Tyr182His)
c.151T>C (p.Tyr51His)
n.712T>C
c.502T>C (p.Tyr168His)
c.643T>C (n.643T>C)
c.640T>C (p.Tyr214His)
3g.93905841A>TCA353673496PROS1c.544T>A (p.Tyr182Asn)
c.151T>A (p.Tyr51Asn)
n.712T>A
c.502T>A (p.Tyr168Asn)
c.643T>A (n.643T>A)
c.640T>A (p.Tyr214Asn)
3g.93905842A>CCA353673498PROS1c.543T>G (p.Ser181Arg)
c.150T>G (p.Ser50Arg)
n.711T>G
c.501T>G (p.Ser167Arg)
c.642T>G (n.642T>G)
c.639T>G (p.Ser213Arg)
3g.93905842A>GCA434626222PROS1c.543T>C (p.Ser181=)
c.150T>C (p.Ser50=)
n.711T>C
c.501T>C (p.Ser167=)
c.642T>C (n.642T>C)
c.639T>C (p.Ser213=)
3g.93905842A>TCA353673497PROS1c.543T>A (p.Ser181Arg)
c.150T>A (p.Ser50Arg)
n.711T>A
c.501T>A (p.Ser167Arg)
c.642T>A (n.642T>A)
c.639T>A (p.Ser213Arg)
3g.93905843C>ACA353673499PROS1c.542G>T (p.Ser181Ile)
c.149G>T (p.Ser50Ile)
n.710G>T
c.500G>T (p.Ser167Ile)
c.641G>T (n.641G>T)
c.638G>T (p.Ser213Ile)
3g.93905843C>GCA353673500PROS1c.542G>C (p.Ser181Thr)
c.149G>C (p.Ser50Thr)
n.710G>C
c.500G>C (p.Ser167Thr)
c.641G>C (n.641G>C)
c.638G>C (p.Ser213Thr)
 gnomAD v4
3g.93905843C>TCA353673501PROS1c.542G>A (p.Ser181Asn)
c.149G>A (p.Ser50Asn)
n.710G>A
c.500G>A (p.Ser167Asn)
c.641G>A (n.641G>A)
c.638G>A (p.Ser213Asn)
3g.93905844T>ACA353673502PROS1c.541A>T (p.Ser181Cys)
c.148A>T (p.Ser50Cys)
n.709A>T
c.499A>T (p.Ser167Cys)
c.640A>T (n.640A>T)
c.637A>T (p.Ser213Cys)
3g.93905844T>CCA353673503PROS1c.541A>G (p.Ser181Gly)
c.148A>G (p.Ser50Gly)
n.709A>G
c.499A>G (p.Ser167Gly)
c.640A>G (n.640A>G)
c.637A>G (p.Ser213Gly)
 dbSNP gnomAD v4
3g.93905844T>GCA353673504PROS1c.541A>C (p.Ser181Arg)
c.148A>C (p.Ser50Arg)
n.709A>C
c.499A>C (p.Ser167Arg)
c.640A>C (n.640A>C)
c.637A>C (p.Ser213Arg)
3g.93905844T=CA1385042603PROS1c.541A= (p.Ser181=)
c.148A= (p.Ser50=)
n.709A=
c.499A= (p.Ser167=)
c.640A= (n.640A=)
c.637A= (p.Ser213=)
3g.93905845T>ACA434626226PROS1c.540A>T (p.Gly180=)
c.147A>T (p.Gly49=)
n.708A>T
c.498A>T (p.Gly166=)
c.639A>T (n.639A>T)
c.636A>T (p.Gly212=)
3g.93905845T>CCA434626227PROS1c.540A>G (p.Gly180=)
c.147A>G (p.Gly49=)
n.708A>G
c.498A>G (p.Gly166=)
c.639A>G (n.639A>G)
c.636A>G (p.Gly212=)
3g.93905845T>GCA434626228PROS1c.540A>C (p.Gly180=)
c.147A>C (p.Gly49=)
n.708A>C
c.498A>C (p.Gly166=)
c.639A>C (n.639A>C)
c.636A>C (p.Gly212=)
3g.93905846C>ACA353673507PROS1c.539G>T (p.Gly180Val)
c.146G>T (p.Gly49Val)
n.707G>T
c.497G>T (p.Gly166Val)
c.638G>T (n.638G>T)
c.635G>T (p.Gly212Val)
3g.93905846C>GCA353673505PROS1c.539G>C (p.Gly180Ala)
c.146G>C (p.Gly49Ala)
n.707G>C
c.497G>C (p.Gly166Ala)
c.638G>C (n.638G>C)
c.635G>C (p.Gly212Ala)
3g.93905846C>TCA353673506PROS1c.539G>A (p.Gly180Glu)
c.146G>A (p.Gly49Glu)
n.707G>A
c.497G>A (p.Gly166Glu)
c.638G>A (n.638G>A)
c.635G>A (p.Gly212Glu)
3g.93905847C>ACA353673508PROS1c.538G>T (p.Gly180Ter)
c.145G>T (p.Gly49Ter)
n.706G>T
c.496G>T (p.Gly166Ter)
c.637G>T (n.637G>T)
c.634G>T (p.Gly212Ter)
3g.93905847C=CA1385042604PROS1c.538G= (p.Gly180=)
c.145G= (p.Gly49=)
n.706G=
c.496G= (p.Gly166=)
c.637G= (n.637G=)
c.634G= (p.Gly212=)
3g.93905847C>GCA353673509PROS1c.538G>C (p.Gly180Arg)
c.145G>C (p.Gly49Arg)
n.706G>C
c.496G>C (p.Gly166Arg)
c.637G>C (n.637G>C)
c.634G>C (p.Gly212Arg)
3g.93905847C>TCA353673510PROS1c.538G>A (p.Gly180Arg)
c.145G>A (p.Gly49Arg)
n.706G>A
c.496G>A (p.Gly166Arg)
c.637G>A (n.637G>A)
c.634G>A (p.Gly212Arg)
 ClinVar dbSNP
3g.93905848A>CCA434626233PROS1c.537T>G (p.Pro179=)
c.144T>G (p.Pro48=)
n.705T>G
c.495T>G (p.Pro165=)
c.636T>G (n.636T>G)
c.633T>G (p.Pro211=)
3g.93905848A>GCA434626234PROS1c.537T>C (p.Pro179=)
c.144T>C (p.Pro48=)
n.705T>C
c.495T>C (p.Pro165=)
c.636T>C (n.636T>C)
c.633T>C (p.Pro211=)
3g.93905848A>TCA434626236PROS1c.537T>A (p.Pro179=)
c.144T>A (p.Pro48=)
n.705T>A
c.495T>A (p.Pro165=)
c.636T>A (n.636T>A)
c.633T>A (p.Pro211=)
3g.93905849G>ACA353673511PROS1c.536C>T (p.Pro179Leu)
c.143C>T (p.Pro48Leu)
n.704C>T
c.494C>T (p.Pro165Leu)
c.635C>T (n.635C>T)
c.632C>T (p.Pro211Leu)
3g.93905849G>CCA2503455PROS1c.536C>G (p.Pro179Arg)
c.143C>G (p.Pro48Arg)
n.704C>G
c.494C>G (p.Pro165Arg)
c.635C>G (n.635C>G)
c.632C>G (p.Pro211Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905849G=CA1385042605PROS1c.536C= (p.Pro179=)
c.143C= (p.Pro48=)
n.704C=
c.494C= (p.Pro165=)
c.635C= (n.635C=)
c.632C= (p.Pro211=)
3g.93905849G>TCA353673512PROS1c.536C>A (p.Pro179His)
c.143C>A (p.Pro48His)
n.704C>A
c.494C>A (p.Pro165His)
c.635C>A (n.635C>A)
c.632C>A (p.Pro211His)
3g.93905850G>ACA353673513PROS1c.535C>T (p.Pro179Ser)
c.142C>T (p.Pro48Ser)
n.703C>T
c.493C>T (p.Pro165Ser)
c.634C>T (n.634C>T)
c.631C>T (p.Pro211Ser)
3g.93905850G>CCA353673514PROS1c.535C>G (p.Pro179Ala)
c.142C>G (p.Pro48Ala)
n.703C>G
c.493C>G (p.Pro165Ala)
c.634C>G (n.634C>G)
c.631C>G (p.Pro211Ala)
3g.93905850G=CA1385042606PROS1c.535C= (p.Pro179=)
c.142C= (p.Pro48=)
n.703C=
c.493C= (p.Pro165=)
c.634C= (n.634C=)
c.631C= (p.Pro211=)
3g.93905850G>TCA353673515PROS1c.535C>A (p.Pro179Thr)
c.142C>A (p.Pro48Thr)
n.703C>A
c.493C>A (p.Pro165Thr)
c.634C>A (n.634C>A)
c.631C>A (p.Pro211Thr)
 dbSNP
3g.93905851T>ACA434626237PROS1c.534A>T (p.Thr178=)
c.141A>T (p.Thr47=)
n.702A>T
c.492A>T (p.Thr164=)
c.633A>T (n.633A>T)
c.630A>T (p.Thr210=)
3g.93905851T>CCA434626240PROS1c.534A>G (p.Thr178=)
c.141A>G (p.Thr47=)
n.702A>G
c.492A>G (p.Thr164=)
c.633A>G (n.633A>G)
c.630A>G (p.Thr210=)
3g.93905851T>GCA434626242PROS1c.534A>C (p.Thr178=)
c.141A>C (p.Thr47=)
n.702A>C
c.492A>C (p.Thr164=)
c.633A>C (n.633A>C)
c.630A>C (p.Thr210=)
 gnomAD v4
3g.93905852G>ACA353673516PROS1c.533C>T (p.Thr178Ile)
c.140C>T (p.Thr47Ile)
n.701C>T
c.491C>T (p.Thr164Ile)
c.632C>T (n.632C>T)
c.629C>T (p.Thr210Ile)
 dbSNP gnomAD v4
3g.93905852G>CCA353673517PROS1c.533C>G (p.Thr178Arg)
c.140C>G (p.Thr47Arg)
n.701C>G
c.491C>G (p.Thr164Arg)
c.632C>G (n.632C>G)
c.629C>G (p.Thr210Arg)
3g.93905852G=CA1385042607PROS1c.533C= (p.Thr178=)
c.140C= (p.Thr47=)
n.701C=
c.491C= (p.Thr164=)
c.632C= (n.632C=)
c.629C= (p.Thr210=)
3g.93905852G>TCA353673518PROS1c.533C>A (p.Thr178Lys)
c.140C>A (p.Thr47Lys)
n.701C>A
c.491C>A (p.Thr164Lys)
c.632C>A (n.632C>A)
c.629C>A (p.Thr210Lys)
3g.93905853T>ACA353673519PROS1c.532A>T (p.Thr178Ser)
c.139A>T (p.Thr47Ser)
n.700A>T
c.490A>T (p.Thr164Ser)
c.631A>T (n.631A>T)
c.628A>T (p.Thr210Ser)
3g.93905853T>CCA353673521PROS1c.532A>G (p.Thr178Ala)
c.139A>G (p.Thr47Ala)
n.700A>G
c.490A>G (p.Thr164Ala)
c.631A>G (n.631A>G)
c.628A>G (p.Thr210Ala)
3g.93905853T>GCA353673520PROS1c.532A>C (p.Thr178Pro)
c.139A>C (p.Thr47Pro)
n.700A>C
c.490A>C (p.Thr164Pro)
c.631A>C (n.631A>C)
c.628A>C (p.Thr210Pro)
3g.93905854A>CCA353673522PROS1c.531T>G (p.Asn177Lys)
c.138T>G (p.Asn46Lys)
n.699T>G
c.489T>G (p.Asn163Lys)
c.630T>G (n.630T>G)
c.627T>G (p.Asn209Lys)
3g.93905854A>GCA434626247PROS1c.531T>C (p.Asn177=)
c.138T>C (p.Asn46=)
n.699T>C
c.489T>C (p.Asn163=)
c.630T>C (n.630T>C)
c.627T>C (p.Asn209=)
 COSMIC
3g.93905854A>TCA353673523PROS1c.531T>A (p.Asn177Lys)
c.138T>A (p.Asn46Lys)
n.699T>A
c.489T>A (p.Asn163Lys)
c.630T>A (n.630T>A)
c.627T>A (p.Asn209Lys)
3g.93905855T>ACA353673524PROS1c.530A>T (p.Asn177Ile)
c.137A>T (p.Asn46Ile)
n.698A>T
c.488A>T (p.Asn163Ile)
c.629A>T (n.629A>T)
c.626A>T (p.Asn209Ile)
3g.93905855T>CCA353673525PROS1c.530A>G (p.Asn177Ser)
c.137A>G (p.Asn46Ser)
n.698A>G
c.488A>G (p.Asn163Ser)
c.629A>G (n.629A>G)
c.626A>G (p.Asn209Ser)
3g.93905855T>GCA353673526PROS1c.530A>C (p.Asn177Thr)
c.137A>C (p.Asn46Thr)
n.698A>C
c.488A>C (p.Asn163Thr)
c.629A>C (n.629A>C)
c.626A>C (p.Asn209Thr)
3g.93905856T>ACA353673527PROS1c.529A>T (p.Asn177Tyr)
c.136A>T (p.Asn46Tyr)
n.697A>T
c.487A>T (p.Asn163Tyr)
c.628A>T (n.628A>T)
c.625A>T (p.Asn209Tyr)
3g.93905856T>CCA2503456PROS1c.529A>G (p.Asn177Asp)
c.136A>G (p.Asn46Asp)
n.697A>G
c.487A>G (p.Asn163Asp)
c.628A>G (n.628A>G)
c.625A>G (p.Asn209Asp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905856T>GCA353673528PROS1c.529A>C (p.Asn177His)
c.136A>C (p.Asn46His)
n.697A>C
c.487A>C (p.Asn163His)
c.628A>C (n.628A>C)
c.625A>C (p.Asn209His)
 gnomAD v4
3g.93905856T=CA1385042608PROS1c.529A= (p.Asn177=)
c.136A= (p.Asn46=)
n.697A=
c.487A= (p.Asn163=)
c.628A= (n.628A=)
c.625A= (p.Asn209=)
3g.93905857A>CCA353673529PROS1c.528T>G (p.Asp176Glu)
c.135T>G (p.Asp45Glu)
n.696T>G
c.486T>G (p.Asp162Glu)
c.627T>G (n.627T>G)
c.624T>G (p.Asp208Glu)
3g.93905857A>GCA434626254PROS1c.528T>C (p.Asp176=)
c.135T>C (p.Asp45=)
n.696T>C
c.486T>C (p.Asp162=)
c.627T>C (n.627T>C)
c.624T>C (p.Asp208=)
3g.93905857A>TCA353673530PROS1c.528T>A (p.Asp176Glu)
c.135T>A (p.Asp45Glu)
n.696T>A
c.486T>A (p.Asp162Glu)
c.627T>A (n.627T>A)
c.624T>A (p.Asp208Glu)
3g.93905858T>ACA353673531PROS1c.527A>T (p.Asp176Val)
c.134A>T (p.Asp45Val)
n.695A>T
c.485A>T (p.Asp162Val)
c.626A>T (n.626A>T)
c.623A>T (p.Asp208Val)
3g.93905858T>CCA353673532PROS1c.527A>G (p.Asp176Gly)
c.134A>G (p.Asp45Gly)
n.695A>G
c.485A>G (p.Asp162Gly)
c.626A>G (n.626A>G)
c.623A>G (p.Asp208Gly)
 gnomAD v4
3g.93905858T>GCA353673533PROS1c.527A>C (p.Asp176Ala)
c.134A>C (p.Asp45Ala)
n.695A>C
c.485A>C (p.Asp162Ala)
c.626A>C (n.626A>C)
c.623A>C (p.Asp208Ala)
3g.93905859C>ACA353673534PROS1c.526G>T (p.Asp176Tyr)
c.133G>T (p.Asp45Tyr)
n.694G>T
c.484G>T (p.Asp162Tyr)
c.625G>T (n.625G>T)
c.622G>T (p.Asp208Tyr)
 dbSNP gnomAD v2 gnomAD v4
3g.93905859C=CA1385042609PROS1c.526G= (p.Asp176=)
c.133G= (p.Asp45=)
n.694G=
c.484G= (p.Asp162=)
c.625G= (n.625G=)
c.622G= (p.Asp208=)
3g.93905859C>GCA2503457PROS1c.526G>C (p.Asp176His)
c.133G>C (p.Asp45His)
n.694G>C
c.484G>C (p.Asp162His)
c.625G>C (n.625G>C)
c.622G>C (p.Asp208His)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.93905859C>TCA353673535PROS1c.526G>A (p.Asp176Asn)
c.133G>A (p.Asp45Asn)
n.694G>A
c.484G>A (p.Asp162Asn)
c.625G>A (n.625G>A)
c.622G>A (p.Asp208Asn)
3g.93905860A=CA1385042610PROS1c.525T= (p.Cys175=)
c.132T= (p.Cys44=)
n.693T=
c.483T= (p.Cys161=)
c.624T= (n.624T=)
c.621T= (p.Cys207=)
3g.93905860A>CCA353673536PROS1c.525T>G (p.Cys175Trp)
c.132T>G (p.Cys44Trp)
n.693T>G
c.483T>G (p.Cys161Trp)
c.624T>G (n.624T>G)
c.621T>G (p.Cys207Trp)
 dbSNP gnomAD v2 gnomAD v4
3g.93905860A>GCA434626255PROS1c.525T>C (p.Cys175=)
c.132T>C (p.Cys44=)
n.693T>C
c.483T>C (p.Cys161=)
c.624T>C (n.624T>C)
c.621T>C (p.Cys207=)
3g.93905860A>TCA353673537PROS1c.525T>A (p.Cys175Ter)
c.132T>A (p.Cys44Ter)
n.693T>A
c.483T>A (p.Cys161Ter)
c.624T>A (n.624T>A)
c.621T>A (p.Cys207Ter)
3g.93905861C>ACA353673538PROS1c.524G>T (p.Cys175Phe)
c.131G>T (p.Cys44Phe)
n.692G>T
c.482G>T (p.Cys161Phe)
c.623G>T (n.623G>T)
c.620G>T (p.Cys207Phe)
3g.93905861C>GCA353673539PROS1c.524G>C (p.Cys175Ser)
c.131G>C (p.Cys44Ser)
n.692G>C
c.482G>C (p.Cys161Ser)
c.623G>C (n.623G>C)
c.620G>C (p.Cys207Ser)
 gnomAD v4
3g.93905861C>TCA353673540PROS1c.524G>A (p.Cys175Tyr)
c.131G>A (p.Cys44Tyr)
n.692G>A
c.482G>A (p.Cys161Tyr)
c.623G>A (n.623G>A)
c.620G>A (p.Cys207Tyr)
3g.93905862A>CCA353673541PROS1c.523T>G (p.Cys175Gly)
c.130T>G (p.Cys44Gly)
n.691T>G
c.481T>G (p.Cys161Gly)
c.622T>G (n.622T>G)
c.619T>G (p.Cys207Gly)
3g.93905862A>GCA353673542PROS1c.523T>C (p.Cys175Arg)
c.130T>C (p.Cys44Arg)
n.691T>C
c.481T>C (p.Cys161Arg)
c.622T>C (n.622T>C)
c.619T>C (p.Cys207Arg)
 gnomAD v4
3g.93905862A>TCA353673543PROS1c.523T>A (p.Cys175Ser)
c.130T>A (p.Cys44Ser)
n.691T>A
c.481T>A (p.Cys161Ser)
c.622T>A (n.622T>A)
c.619T>A (p.Cys207Ser)
3g.93905864delCA2757501085PROS1c.523del (p.Cys175ValfsTer?)
c.523del (p.Cys175ValfsTer18)
c.130del (p.Cys44ValfsTer?)
n.691del
c.481del (p.Cys161ValfsTer?)
c.622del (n.622del)
c.619del (p.Cys207ValfsTer?)
3g.93905863A>CCA353673544PROS1c.522T>G (p.Ile174Met)
c.129T>G (p.Ile43Met)
n.690T>G
c.480T>G (p.Ile160Met)
c.621T>G (n.621T>G)
c.618T>G (p.Ile206Met)
3g.93905863A>GCA434626259PROS1c.522T>C (p.Ile174=)
c.129T>C (p.Ile43=)
n.690T>C
c.480T>C (p.Ile160=)
c.621T>C (n.621T>C)
c.618T>C (p.Ile206=)
3g.93905863A>TCA434626258PROS1c.522T>A (p.Ile174=)
c.129T>A (p.Ile43=)
n.690T>A
c.480T>A (p.Ile160=)
c.621T>A (n.621T>A)
c.618T>A (p.Ile206=)
3g.93905864A>CCA353673547PROS1c.521T>G (p.Ile174Ser)
c.128T>G (p.Ile43Ser)
n.689T>G
c.479T>G (p.Ile160Ser)
c.620T>G (n.620T>G)
c.617T>G (p.Ile206Ser)
3g.93905864A>GCA353673546PROS1c.521T>C (p.Ile174Thr)
c.128T>C (p.Ile43Thr)
n.689T>C
c.479T>C (p.Ile160Thr)
c.620T>C (n.620T>C)
c.617T>C (p.Ile206Thr)
3g.93905864A>TCA353673545PROS1c.521T>A (p.Ile174Asn)
c.128T>A (p.Ile43Asn)
n.689T>A
c.479T>A (p.Ile160Asn)
c.620T>A (n.620T>A)
c.617T>A (p.Ile206Asn)
3g.93905865T>ACA353673548PROS1c.520A>T (p.Ile174Phe)
c.127A>T (p.Ile43Phe)
n.688A>T
c.478A>T (p.Ile160Phe)
c.619A>T (n.619A>T)
c.616A>T (p.Ile206Phe)
3g.93905865T>CCA353673550PROS1c.520A>G (p.Ile174Val)
c.127A>G (p.Ile43Val)
n.688A>G
c.478A>G (p.Ile160Val)
c.619A>G (n.619A>G)
c.616A>G (p.Ile206Val)
3g.93905865T>GCA353673549PROS1c.520A>C (p.Ile174Leu)
c.127A>C (p.Ile43Leu)
n.688A>C
c.478A>C (p.Ile160Leu)
c.619A>C (n.619A>C)
c.616A>C (p.Ile206Leu)
3g.93905866T>ACA353673551PROS1c.519A>T (p.Gln173His)
c.126A>T (p.Gln42His)
n.687A>T
c.477A>T (p.Gln159His)
c.618A>T (n.618A>T)
c.615A>T (p.Gln205His)
3g.93905866T>CCA434626261PROS1c.519A>G (p.Gln173=)
c.126A>G (p.Gln42=)
n.687A>G
c.477A>G (p.Gln159=)
c.618A>G (n.618A>G)
c.615A>G (p.Gln205=)
3g.93905866T>GCA353673552PROS1c.519A>C (p.Gln173His)
c.126A>C (p.Gln42His)
n.687A>C
c.477A>C (p.Gln159His)
c.618A>C (n.618A>C)
c.615A>C (p.Gln205His)
3g.93905867T>ACA353673553PROS1c.518A>T (p.Gln173Leu)
c.125A>T (p.Gln42Leu)
n.686A>T
c.476A>T (p.Gln159Leu)
c.617A>T (n.617A>T)
c.614A>T (p.Gln205Leu)
3g.93905867T>CCA353673554PROS1c.518A>G (p.Gln173Arg)
c.125A>G (p.Gln42Arg)
n.686A>G
c.476A>G (p.Gln159Arg)
c.617A>G (n.617A>G)
c.614A>G (p.Gln205Arg)
3g.93905867T>GCA353673555PROS1c.518A>C (p.Gln173Pro)
c.125A>C (p.Gln42Pro)
n.686A>C
c.476A>C (p.Gln159Pro)
c.617A>C (n.617A>C)
c.614A>C (p.Gln205Pro)
3g.93905868G>ACA353673556PROS1c.517C>T (p.Gln173Ter)
c.124C>T (p.Gln42Ter)
n.685C>T
c.475C>T (p.Gln159Ter)
c.616C>T (n.616C>T)
c.613C>T (p.Gln205Ter)
3g.93905868G>CCA353673557PROS1c.517C>G (p.Gln173Glu)
c.124C>G (p.Gln42Glu)
n.685C>G
c.475C>G (p.Gln159Glu)
c.616C>G (n.616C>G)
c.613C>G (p.Gln205Glu)
3g.93905868G>TCA353673558PROS1c.517C>A (p.Gln173Lys)
c.124C>A (p.Gln42Lys)
n.685C>A
c.475C>A (p.Gln159Lys)
c.616C>A (n.616C>A)
c.613C>A (p.Gln205Lys)
 ClinVar dbSNP gnomAD v4
3g.93905869A>CCA353673559PROS1c.516T>G (p.Ser172Arg)
c.123T>G (p.Ser41Arg)
n.684T>G
c.474T>G (p.Ser158Arg)
c.615T>G (n.615T>G)
c.612T>G (p.Ser204Arg)
3g.93905869A>GCA434626271PROS1c.516T>C (p.Ser172=)
c.123T>C (p.Ser41=)
n.684T>C
c.474T>C (p.Ser158=)
c.615T>C (n.615T>C)
c.612T>C (p.Ser204=)
3g.93905869A>TCA353673560PROS1c.516T>A (p.Ser172Arg)
c.123T>A (p.Ser41Arg)
n.684T>A
c.474T>A (p.Ser158Arg)
c.615T>A (n.615T>A)
c.612T>A (p.Ser204Arg)
3g.93905870C>ACA353673563PROS1c.515G>T (p.Ser172Ile)
c.122G>T (p.Ser41Ile)
n.683G>T
c.473G>T (p.Ser158Ile)
c.614G>T (n.614G>T)
c.611G>T (p.Ser204Ile)
3g.93905870C>GCA353673562PROS1c.515G>C (p.Ser172Thr)
c.122G>C (p.Ser41Thr)
n.683G>C
c.473G>C (p.Ser158Thr)
c.614G>C (n.614G>C)
c.611G>C (p.Ser204Thr)
3g.93905870C>TCA353673561PROS1c.515G>A (p.Ser172Asn)
c.122G>A (p.Ser41Asn)
n.683G>A
c.473G>A (p.Ser158Asn)
c.614G>A (n.614G>A)
c.611G>A (p.Ser204Asn)
3g.93905871T>ACA353673564PROS1c.514A>T (p.Ser172Cys)
c.121A>T (p.Ser41Cys)
n.682A>T
c.472A>T (p.Ser158Cys)
c.613A>T (n.613A>T)
c.610A>T (p.Ser204Cys)
3g.93905871T>CCA353673565PROS1c.514A>G (p.Ser172Gly)
c.121A>G (p.Ser41Gly)
n.682A>G
c.472A>G (p.Ser158Gly)
c.613A>G (n.613A>G)
c.610A>G (p.Ser204Gly)
 dbSNP gnomAD v2 gnomAD v4
3g.93905871T>GCA353673566PROS1c.514A>C (p.Ser172Arg)
c.121A>C (p.Ser41Arg)
n.682A>C
c.472A>C (p.Ser158Arg)
c.613A>C (n.613A>C)
c.610A>C (p.Ser204Arg)
3g.93905871T=CA1385042611PROS1c.514A= (p.Ser172=)
c.121A= (p.Ser41=)
n.682A=
c.472A= (p.Ser158=)
c.613A= (n.613A=)
c.610A= (p.Ser204=)
3g.93905872G>ACA434626274PROS1c.513C>T (p.Cys171=)
c.120C>T (p.Cys40=)
n.681C>T
c.471C>T (p.Cys157=)
c.612C>T (n.612C>T)
c.609C>T (p.Cys203=)
3g.93905872G>CCA353673567PROS1c.513C>G (p.Cys171Trp)
c.120C>G (p.Cys40Trp)
n.681C>G
c.471C>G (p.Cys157Trp)
c.612C>G (n.612C>G)
c.609C>G (p.Cys203Trp)
3g.93905872G>TCA353673568PROS1c.513C>A (p.Cys171Ter)
c.120C>A (p.Cys40Ter)
n.681C>A
c.471C>A (p.Cys157Ter)
c.612C>A (n.612C>A)
c.609C>A (p.Cys203Ter)
3g.93905873C>ACA353673569PROS1c.512G>T (p.Cys171Phe)
c.119G>T (p.Cys40Phe)
n.680G>T
c.470G>T (p.Cys157Phe)
c.611G>T (n.611G>T)
c.608G>T (p.Cys203Phe)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
3g.93905873C=CA1385042612PROS1c.512G= (p.Cys171=)
c.119G= (p.Cys40=)
n.680G=
c.470G= (p.Cys157=)
c.611G= (n.611G=)
c.608G= (p.Cys203=)
3g.93905873C>GCA353673570PROS1c.512G>C (p.Cys171Ser)
c.119G>C (p.Cys40Ser)
n.680G>C
c.470G>C (p.Cys157Ser)
c.611G>C (n.611G>C)
c.608G>C (p.Cys203Ser)
 ClinVar dbSNP
3g.93905873C>TCA353673571PROS1c.512G>A (p.Cys171Tyr)
c.119G>A (p.Cys40Tyr)
n.680G>A
c.470G>A (p.Cys157Tyr)
c.611G>A (n.611G>A)
c.608G>A (p.Cys203Tyr)
3g.93905874A=CA1385042613PROS1c.511T= (p.Cys171=)
c.118T= (p.Cys40=)
n.679T=
c.469T= (p.Cys157=)
c.610T= (n.610T=)
c.607T= (p.Cys203=)
3g.93905874A>CCA353673572PROS1c.511T>G (p.Cys171Gly)
c.118T>G (p.Cys40Gly)
n.679T>G
c.469T>G (p.Cys157Gly)
c.610T>G (n.610T>G)
c.607T>G (p.Cys203Gly)
 ClinVar dbSNP
3g.93905874A>GCA353673573PROS1c.511T>C (p.Cys171Arg)
c.118T>C (p.Cys40Arg)
n.679T>C
c.469T>C (p.Cys157Arg)
c.610T>C (n.610T>C)
c.607T>C (p.Cys203Arg)
3g.93905874A>TCA353673574PROS1c.511T>A (p.Cys171Ser)
c.118T>A (p.Cys40Ser)
n.679T>A
c.469T>A (p.Cys157Ser)
c.610T>A (n.610T>A)
c.607T>A (p.Cys203Ser)
3g.93905875A>CCA434626278PROS1c.510T>G (p.Gly170=)
c.117T>G (p.Gly39=)
n.678T>G
c.468T>G (p.Gly156=)
c.609T>G (n.609T>G)
c.606T>G (p.Gly202=)
3g.93905875A>GCA434626280PROS1c.510T>C (p.Gly170=)
c.117T>C (p.Gly39=)
n.678T>C
c.468T>C (p.Gly156=)
c.609T>C (n.609T>C)
c.606T>C (p.Gly202=)
3g.93905875A>TCA434626284PROS1c.510T>A (p.Gly170=)
c.117T>A (p.Gly39=)
n.678T>A
c.468T>A (p.Gly156=)
c.609T>A (n.609T>A)
c.606T>A (p.Gly202=)
3g.93905876C>ACA353673576PROS1c.509G>T (p.Gly170Val)
c.116G>T (p.Gly39Val)
n.677G>T
c.467G>T (p.Gly156Val)
c.608G>T (n.608G>T)
c.605G>T (p.Gly202Val)
3g.93905876C>GCA353673577PROS1c.509G>C (p.Gly170Ala)
c.116G>C (p.Gly39Ala)
n.677G>C
c.467G>C (p.Gly156Ala)
c.608G>C (n.608G>C)
c.605G>C (p.Gly202Ala)
3g.93905876C>TCA353673575PROS1c.509G>A (p.Gly170Asp)
c.116G>A (p.Gly39Asp)
n.677G>A
c.467G>A (p.Gly156Asp)
c.608G>A (n.608G>A)
c.605G>A (p.Gly202Asp)
3g.93905877C>ACA353673578PROS1c.508G>T (p.Gly170Cys)
c.115G>T (p.Gly39Cys)
n.676G>T
c.466G>T (p.Gly156Cys)
c.607G>T (n.607G>T)
c.604G>T (p.Gly202Cys)
 COSMIC
3g.93905877C>GCA353673579PROS1c.508G>C (p.Gly170Arg)
c.115G>C (p.Gly39Arg)
n.676G>C
c.466G>C (p.Gly156Arg)
c.607G>C (n.607G>C)
c.604G>C (p.Gly202Arg)
3g.93905877C>TCA353673580PROS1c.508G>A (p.Gly170Ser)
c.115G>A (p.Gly39Ser)
n.676G>A
c.466G>A (p.Gly156Ser)
c.607G>A (n.607G>A)
c.604G>A (p.Gly202Ser)
3g.93905878T>ACA434626287PROS1c.507A>T (p.Gly169=)
c.114A>T (p.Gly38=)
n.675A>T
c.465A>T (p.Gly155=)
c.606A>T (n.606A>T)
c.603A>T (p.Gly201=)
 gnomAD v4
3g.93905878T>CCA434626288PROS1c.507A>G (p.Gly169=)
c.114A>G (p.Gly38=)
n.675A>G
c.465A>G (p.Gly155=)
c.606A>G (n.606A>G)
c.603A>G (p.Gly201=)
3g.93905878T>GCA434626289PROS1c.507A>C (p.Gly169=)
c.114A>C (p.Gly38=)
n.675A>C
c.465A>C (p.Gly155=)
c.606A>C (n.606A>C)
c.603A>C (p.Gly201=)
3g.93905879C>ACA353673581PROS1c.506G>T (p.Gly169Val)
c.113G>T (p.Gly38Val)
n.674G>T
c.464G>T (p.Gly155Val)
c.605G>T (n.605G>T)
c.602G>T (p.Gly201Val)
 dbSNP gnomAD v2 gnomAD v4
3g.93905879C=CA1385042614PROS1c.506G= (p.Gly169=)
c.113G= (p.Gly38=)
n.674G=
c.464G= (p.Gly155=)
c.605G= (n.605G=)
c.602G= (p.Gly201=)
3g.93905879C>GCA2503458PROS1c.506G>C (p.Gly169Ala)
c.113G>C (p.Gly38Ala)
n.674G>C
c.464G>C (p.Gly155Ala)
c.605G>C (n.605G>C)
c.602G>C (p.Gly201Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.93905879C>TCA353673582PROS1c.506G>A (p.Gly169Glu)
c.113G>A (p.Gly38Glu)
n.674G>A
c.464G>A (p.Gly155Glu)
c.605G>A (n.605G>A)
c.602G>A (p.Gly201Glu)
 gnomAD v4
3g.93905880C>ACA353673585PROS1c.505G>T (p.Gly169Ter)
c.112G>T (p.Gly38Ter)
n.673G>T
c.463G>T (p.Gly155Ter)
c.604G>T (n.604G>T)
c.601G>T (p.Gly201Ter)
3g.93905880C>GCA353673583PROS1c.505G>C (p.Gly169Arg)
c.112G>C (p.Gly38Arg)
n.673G>C
c.463G>C (p.Gly155Arg)
c.604G>C (n.604G>C)
c.601G>C (p.Gly201Arg)
3g.93905880C>TCA353673584PROS1c.505G>A (p.Gly169Arg)
c.112G>A (p.Gly38Arg)
n.673G>A
c.463G>A (p.Gly155Arg)
c.604G>A (n.604G>A)
c.601G>A (p.Gly201Arg)
3g.93905881A>CCA353673586PROS1c.504T>G (p.Asn168Lys)
c.111T>G (p.Asn37Lys)
n.672T>G
c.462T>G (p.Asn154Lys)
c.603T>G (n.603T>G)
c.600T>G (p.Asn200Lys)
3g.93905881A>GCA434626292PROS1c.504T>C (p.Asn168=)
c.111T>C (p.Asn37=)
n.672T>C
c.462T>C (p.Asn154=)
c.603T>C (n.603T>C)
c.600T>C (p.Asn200=)
3g.93905881A>TCA353673587PROS1c.504T>A (p.Asn168Lys)
c.111T>A (p.Asn37Lys)
n.672T>A
c.462T>A (p.Asn154Lys)
c.603T>A (n.603T>A)
c.600T>A (p.Asn200Lys)
3g.93905882T>ACA353673588PROS1c.503A>T (p.Asn168Ile)
c.110A>T (p.Asn37Ile)
n.671A>T
c.461A>T (p.Asn154Ile)
c.602A>T (n.602A>T)
c.599A>T (p.Asn200Ile)
3g.93905882T>CCA2503459PROS1c.503A>G (p.Asn168Ser)
c.110A>G (p.Asn37Ser)
n.671A>G
c.461A>G (p.Asn154Ser)
c.602A>G (n.602A>G)
c.599A>G (p.Asn200Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905882T>GCA353673589PROS1c.503A>C (p.Asn168Thr)
c.110A>C (p.Asn37Thr)
n.671A>C
c.461A>C (p.Asn154Thr)
c.602A>C (n.602A>C)
c.599A>C (p.Asn200Thr)
3g.93905882T=CA1385042615PROS1c.503A= (p.Asn168=)
c.110A= (p.Asn37=)
n.671A=
c.461A= (p.Asn154=)
c.602A= (n.602A=)
c.599A= (p.Asn200=)
3g.93905883T>ACA353673590PROS1c.502A>T (p.Asn168Tyr)
c.109A>T (p.Asn37Tyr)
n.670A>T
c.460A>T (p.Asn154Tyr)
c.601A>T (n.601A>T)
c.598A>T (p.Asn200Tyr)
3g.93905883T>CCA353673592PROS1c.502A>G (p.Asn168Asp)
c.109A>G (p.Asn37Asp)
n.670A>G
c.460A>G (p.Asn154Asp)
c.601A>G (n.601A>G)
c.598A>G (p.Asn200Asp)
3g.93905883T>GCA353673591PROS1c.502A>C (p.Asn168His)
c.109A>C (p.Asn37His)
n.670A>C
c.460A>C (p.Asn154His)
c.601A>C (n.601A>C)
c.598A>C (p.Asn200His)
3g.93905884T>ACA434626299PROS1c.501A>T (p.Ile167=)
c.108A>T (p.Ile36=)
n.669A>T
c.459A>T (p.Ile153=)
c.600A>T (n.600A>T)
c.597A>T (p.Ile199=)
3g.93905884T>CCA2503460PROS1c.501A>G (p.Ile167Met)
c.108A>G (p.Ile36Met)
n.669A>G
c.459A>G (p.Ile153Met)
c.600A>G (n.600A>G)
c.597A>G (p.Ile199Met)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.93905884T>GCA434626302PROS1c.501A>C (p.Ile167=)
c.108A>C (p.Ile36=)
n.669A>C
c.459A>C (p.Ile153=)
c.600A>C (n.600A>C)
c.597A>C (p.Ile199=)
3g.93905884T=CA1385042616PROS1c.501A= (p.Ile167=)
c.108A= (p.Ile36=)
n.669A=
c.459A= (p.Ile153=)
c.600A= (n.600A=)
c.597A= (p.Ile199=)
3g.93905885A>CCA353673593PROS1c.500T>G (p.Ile167Arg)
c.107T>G (p.Ile36Arg)
n.668T>G
c.458T>G (p.Ile153Arg)
c.599T>G (n.599T>G)
c.596T>G (p.Ile199Arg)
3g.93905885A>GCA353673594PROS1c.500T>C (p.Ile167Thr)
c.107T>C (p.Ile36Thr)
n.668T>C
c.458T>C (p.Ile153Thr)
c.599T>C (n.599T>C)
c.596T>C (p.Ile199Thr)
3g.93905885A>TCA353673595PROS1c.500T>A (p.Ile167Lys)
c.107T>A (p.Ile36Lys)
n.668T>A
c.458T>A (p.Ile153Lys)
c.599T>A (n.599T>A)
c.596T>A (p.Ile199Lys)
3g.93905886T>ACA353673596PROS1c.499A>T (p.Ile167Leu)
c.106A>T (p.Ile36Leu)
n.667A>T
c.457A>T (p.Ile153Leu)
c.598A>T (n.598A>T)
c.595A>T (p.Ile199Leu)
3g.93905886T>CCA353673597PROS1c.499A>G (p.Ile167Val)
c.106A>G (p.Ile36Val)
n.667A>G
c.457A>G (p.Ile153Val)
c.598A>G (n.598A>G)
c.595A>G (p.Ile199Val)
 dbSNP gnomAD v4
3g.93905886T>GCA353673598PROS1c.499A>C (p.Ile167Leu)
c.106A>C (p.Ile36Leu)
n.667A>C
c.457A>C (p.Ile153Leu)
c.598A>C (n.598A>C)
c.595A>C (p.Ile199Leu)
3g.93905886T=CA1385042617PROS1c.499A= (p.Ile167=)
c.106A= (p.Ile36=)
n.667A=
c.457A= (p.Ile153=)
c.598A= (n.598A=)
c.595A= (p.Ile199=)
3g.93905887A=CA1385042618PROS1c.498T= (p.Asn166=)
c.105T= (p.Asn35=)
n.666T=
c.456T= (p.Asn152=)
c.597T= (n.597T=)
c.594T= (p.Asn198=)
3g.93905887A>CCA353673599PROS1c.498T>G (p.Asn166Lys)
c.105T>G (p.Asn35Lys)
n.666T>G
c.456T>G (p.Asn152Lys)
c.597T>G (n.597T>G)
c.594T>G (p.Asn198Lys)
 gnomAD v4
3g.93905887A>GCA78490959PROS1c.498T>C (p.Asn166=)
c.105T>C (p.Asn35=)
n.666T>C
c.456T>C (p.Asn152=)
c.597T>C (n.597T>C)
c.594T>C (p.Asn198=)
 dbSNP
3g.93905887A>TCA353673600PROS1c.498T>A (p.Asn166Lys)
c.105T>A (p.Asn35Lys)
n.666T>A
c.456T>A (p.Asn152Lys)
c.597T>A (n.597T>A)
c.594T>A (p.Asn198Lys)
3g.93905888T>ACA353673601PROS1c.497A>T (p.Asn166Ile)
c.104A>T (p.Asn35Ile)
n.665A>T
c.455A>T (p.Asn152Ile)
c.596A>T (n.596A>T)
c.593A>T (p.Asn198Ile)
3g.93905888T>CCA353673602PROS1c.497A>G (p.Asn166Ser)
c.104A>G (p.Asn35Ser)
n.665A>G
c.455A>G (p.Asn152Ser)
c.596A>G (n.596A>G)
c.593A>G (p.Asn198Ser)
 dbSNP gnomAD v2 gnomAD v4
3g.93905888T>GCA353673603PROS1c.497A>C (p.Asn166Thr)
c.104A>C (p.Asn35Thr)
n.665A>C
c.455A>C (p.Asn152Thr)
c.596A>C (n.596A>C)
c.593A>C (p.Asn198Thr)
3g.93905888T=CA1385042619PROS1c.497A= (p.Asn166=)
c.104A= (p.Asn35=)
n.665A=
c.455A= (p.Asn152=)
c.596A= (n.596A=)
c.593A= (p.Asn198=)
3g.93905889T>ACA353673604PROS1c.496A>T (p.Asn166Tyr)
c.103A>T (p.Asn35Tyr)
n.664A>T
c.454A>T (p.Asn152Tyr)
c.595A>T (n.595A>T)
c.592A>T (p.Asn198Tyr)
3g.93905889T>CCA353673605PROS1c.496A>G (p.Asn166Asp)
c.103A>G (p.Asn35Asp)
n.664A>G
c.454A>G (p.Asn152Asp)
c.595A>G (n.595A>G)
c.592A>G (p.Asn198Asp)
3g.93905889T>GCA2503461PROS1c.496A>C (p.Asn166His)
c.103A>C (p.Asn35His)
n.664A>C
c.454A>C (p.Asn152His)
c.595A>C (n.595A>C)
c.592A>C (p.Asn198His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93905889T=CA1385042620PROS1c.496A= (p.Asn166=)
c.103A= (p.Asn35=)
n.664A=
c.454A= (p.Asn152=)
c.595A= (n.595A=)
c.592A= (p.Asn198=)
3g.93905890T>ACA434626315PROS1c.495A>T (p.Ser165=)
c.102A>T (p.Ser34=)
n.663A>T
c.453A>T (p.Ser151=)
c.594A>T (n.594A>T)
c.591A>T (p.Ser197=)
3g.93905890T>CCA434626310PROS1c.495A>G (p.Ser165=)
c.102A>G (p.Ser34=)
n.663A>G
c.453A>G (p.Ser151=)
c.594A>G (n.594A>G)
c.591A>G (p.Ser197=)
3g.93905890T>GCA434626313PROS1c.495A>C (p.Ser165=)
c.102A>C (p.Ser34=)
n.663A>C
c.453A>C (p.Ser151=)
c.594A>C (n.594A>C)
c.591A>C (p.Ser197=)
3g.93905891G>ACA353673608PROS1c.494C>T (p.Ser165Leu)
c.101C>T (p.Ser34Leu)
n.662C>T
c.452C>T (p.Ser151Leu)
c.593C>T (n.593C>T)
c.590C>T (p.Ser197Leu)
 gnomAD v4 COSMIC
3g.93905891G>CCA353673606PROS1c.494C>G (p.Ser165Ter)
c.101C>G (p.Ser34Ter)
n.662C>G
c.452C>G (p.Ser151Ter)
c.593C>G (n.593C>G)
c.590C>G (p.Ser197Ter)
3g.93905891G>TCA353673607PROS1c.494C>A (p.Ser165Ter)
c.101C>A (p.Ser34Ter)
n.662C>A
c.452C>A (p.Ser151Ter)
c.593C>A (n.593C>A)
c.590C>A (p.Ser197Ter)
3g.93905892A>CCA353673609PROS1c.493T>G (p.Ser165Ala)
c.100T>G (p.Ser34Ala)
n.661T>G
c.451T>G (p.Ser151Ala)
c.592T>G (n.592T>G)
c.589T>G (p.Ser197Ala)
3g.93905892A>GCA353673610PROS1c.493T>C (p.Ser165Pro)
c.100T>C (p.Ser34Pro)
n.661T>C
c.451T>C (p.Ser151Pro)
c.592T>C (n.592T>C)
c.589T>C (p.Ser197Pro)
3g.93905892A>TCA353673611PROS1c.493T>A (p.Ser165Thr)
c.100T>A (p.Ser34Thr)
n.661T>A
c.451T>A (p.Ser151Thr)
c.592T>A (n.592T>A)
c.589T>A (p.Ser197Thr)

Number of alleles fetched